From owner-ageing@net.bio.net Sat Jul 01 23:00:00 1995
Path: biosci!rutgers!gatech!howland.reston.ans.net!xlink.net!nntp.gmd.de!news.rwth-aachen.de!news.rhrz.uni-bonn.de!news.uni-stuttgart.de!news.belwue.de!News.Uni-Marburg.DE!usenet
From: Andreas Becker <becker@ps1515.chemie.uni-marburg.de>
Newsgroups: bionet.molbio.ageing
Subject: Mitochondria WWW site
Date: 2 Jul 1995 11:39:20 GMT
Organization: FB Chemie/Biochemie, Phillips-Universitaet, D-35039 MARBURG
Lines: 16
Message-ID: <3t60h8$6fd@surz03.HRZ.Uni-Marburg.DE>
NNTP-Posting-Host: nnex08.ppp.uni-marburg.de
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 1.1N (Windows; I; 16bit)

Is there any site with the topics:
mitochondria
mitochondria and aging

I want to build up a www site where I will mention that topics.
If any one know a www site please tell me.

----------------------------------------------------------------------
Andreas Becker
Arbeitskreis Prof. Kadenbach, FB Chemie/Biochemie, Hans-
Meerwein-Strasse, Philipps-Universitaet, 35043 Marburg, Germany
Phone: privat +49 6421 47304  Labor +49 6421 28 -5721 Fax -2191
eMail: BECKER@ps1515.Chemie.Uni-Marburg.De
WWW  : http://www.chemie.uni-marburg.de/~becker



From owner-ageing@net.bio.net Sun Jul 02 23:00:00 1995
Path: biosci!POSSUM.MURDOCH.EDU.AU!cummins
From: cummins@POSSUM.MURDOCH.EDU.AU (Dr Jim Cummins)
Newsgroups: bionet.molbio.ageing
Subject: Re: Mitochondria WWW site
Date: 2 Jul 1995 17:39:10 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 23
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v01510102ac1ceb87b190@[134.115.81.42]>
NNTP-Posting-Host: net.bio.net

>Is there any site with the topics:
>mitochondria
>mitochondria and aging
>
>I want to build up a www site where I will mention that topics.
>If any one know a www site please tell me.

Try gopher://megasun.bch.umontreal.ca:70/11/Organelles
http://www.hookup.net/mall/aging/agesit59.html


Jim "Spermatology rules o~ o~ o~ o~" Cummins

Associate Professor in Veterinary Anatomy
Murdoch University, Western Australia 6150
Tel +61-9-360 2668, Fax +61-9-310 4144
E mail <cummins@possum.murdoch.edu.au>
URL <http://Numbat.murdoch.edu.au/spermatology/spermhp.html>
"An inordinate fondness for Beetles" (Haldane on God).





From owner-ageing@net.bio.net Tue Jul 04 23:00:00 1995
Path: biosci!bcm!cs.utexas.edu!news.sprintlink.net!gatech!newsjunkie.ans.net!Rezonet.net!titane!comback!nntphost!comback!chatterbox.login.net!doctor_godless
Newsgroups: bionet.molbio.ageing
Message-ID: <1554@chatterbox.login.net>
Reply-To: doctor_godless@chatterbox.login.net (DOCTOR GODLESS)
From: doctor_godless@chatterbox.login.net (DOCTOR GODLESS)
Date: Wed, 05 Jul 1995 06:05:00 GMT
Subject: Re: Searching            
Lines: 12

 I would also like a copy. Please send me one at: 
 
                                Doctor_godless@chatterbox.login.net

It would be much appreciated. I don't want to bother Dr. Post if I can
avoid it. Thanks in advance.
                                        Doc



... There's nothing to fear except nothing itself. -Wagschal  
___ Blue Wave/QWK v2.12


From owner-ageing@net.bio.net Wed Jul 05 23:00:00 1995
Path: biosci!RESUNIX.RI.SICKKIDS.ON.CA!shah
From: shah@RESUNIX.RI.SICKKIDS.ON.CA
Newsgroups: bionet.molbio.ageing
Subject: cell-death meeting
Date: 6 Jul 1995 10:43:40 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 17
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v01510100ac21ce5c91b2@[142.20.6.185]>
NNTP-Posting-Host: net.bio.net

Hi,
I am a PhD graduate student in yeast genetics and very close to graduation.
I have decided that I would like to pursue the field of programmed cell
death for my Post Doc and hopefully future career.  I would love to be able
to go to a cell-death meeting this year to familiarize myself with the
field and get to know the people in the field.  I know that there is a Cold
Spring Harbour meeting coming in September, but I am told that it would be
difficult to attend the meeting since I don't belong to a cell-death lab.
Do you have any advice for me as to how I can attend this meeting, whether
there are any other meeting that I might go to that is not as restricted
and equally informative.  I thank you in advance for your help and
suggestions.

Sherry
shah@resunix.ri.sickkids.on.ca



From owner-ageing@net.bio.net Wed Jul 05 23:00:00 1995
Path: biosci!FREENET.TORONTO.ON.CA!bk772
From: bk772@FREENET.TORONTO.ON.CA (Dmitri Chamchad)
Newsgroups: bionet.molbio.ageing
Subject: pathology/histology job need
Date: 6 Jul 1995 12:27:49 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 112
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.3.89.9507061414.B4074-0100000@bloor>
References: <v01510100ac21ce5c91b2@[142.20.6.185]>
NNTP-Posting-Host: net.bio.net


	My name is Dmitri Chamchad , I'm doctor of medicine.
I had working several years on the problem of aging. I searched 
especially aging of spermatogenic cells in mail gonads, comparison 
between Youngest and oldest models. I search intercellular interaction 
between Leudig cells, Sertolly cells and spermatogenic layer. I did 
find conformity to natural laws in aging process of male gonads, and
as result - method of treatment male sterility syndrome.
If You can help me by any way , I'll be very grateful.


                      R E S U M E

                 SUMMARY OF QUALIFICATION

- selection  tissues for analysis; different methods of tissue
preservation;  preparation of tissues for examination by
ultratome and microtome;

- DNA molecular Biology: Isotope or DIG labeling DNA probes.
Southern, Northern, and Western blots analysis.

- tissue culture: Mammalian cell culture. Specimen preparation
and operation for SEM and TEM.

- chemical methods of tissue colouring using different stains
as haematoxylin and eosin dye, Sudan IV, Feulgen's reaction,
argentum impregnation; fluorescent stains and fluorescent
antibodies; processing tissues using enzymes ( Dnase, RNase,
Phosphothase etc); immunologic method of labeling antibodies;

- quality analysis of microscopic cells, tissues and cells
identification, morphometry, computerized analysing tissues;

-  computer software: Word Perfect; Microsoft Excel, Words,
Works, Windows; programming in Visual Basic, Fortran.

                      WORK EXPERIENCE

11.1986 Histologist. Department of Histology and Embryology of
06.1990 Medical University, Moscow, Russia.

11.1990 Histologist. M.P. "Medinform"
06.1992 Moscow, Russia.

                         EDUCATION

09.1985 Russian Medical University, Moscow, Russia,
02.1992 Paediatric Department. Degree, Medical Doctor.

09.1980 Moscow Medical College
07.1982 Diploma, Registered Nurse

                     LIST OF PUBLICATIONS

1. V.S.Sukhorukov, D.A.Chamchad "definition of spermatogenic
layer maturity level in rats during regeneration or during
intact testicular development" in Archives of AHE-Society
[Archives of Anatomy, Histology and Embryology], 1989, N9, pp
88-91

2. V.S.Sukhorukov, S.B.Tarabryn, D.A.Chamchad "Use of Sertoli
-cells-only syndrome model for investigation of some gonadal
development regularities in "Actual Problems of Medical
Embryology" Siberian Depart. of Medical Academy, AHE-Society,
Irkutsk, 1989


3. V.S.Sukhorukov, S.B.Tarabryn, I.A.Darenkov, A.A.Dreval,
O.V.Volkova, A.K.Polonsky, D.A.Chamchad "Way for male sterility
treatment" Patent request N 48248664/14, priority of May 29,1990

4. V.S.Sukhorukov, S.B.Tarabryn, D.A.Chamchad "Postnatal
SCO-syndrome in rats as a model of paracrine regulation and
regeneration research" 4th Int. Congr. on Vertebrates Biol. 1992
Moscow

5. O.V.Volkova, S.B.Tarabryn, S.B.Sukhorukov, D.A.Chamchad
"Paracrine regulation in male gonads. I. Interactions between
somatic gonadal components." Archives of AHE-Society 1992

6.O. V.Volkova, S.B.Tarabryn, V.S.Sukhorukov, D.A.Chamchad
"Paracrine regulation in male gonads. II About the possibility
of germ cells influence on somatic microenvironment" Archives of
AHE-Society in press.

                    OTHERS

   Permanent resinent of Canada


             REFERENCES (can be send by request):

1. Chief of Department of Histology and Embryology of Russian
   Medical University, Member of Medical Academy D.M. prof.
   Olga  V. Volkova Moscow, Ostrovitanova str. Building N1
   Department of Histology and Embryology tel.(095)-434-4192;

2. Scientific Chief M.D. Ph.D. Docent. Sergey B. Tarabryn
   Moscow, Ostrovitanova str. Building N1
   Department of Histology and Embryology tel.(095)-442-6323
                                              (095)-434-5534
3. General Director M.P. "Medinform" Victor I. Shustov
   Moscow, Bolotnikovskay str.41-96 tel.(095)-433-0520


Dmitri Chamchad
715 Finch ave. west, apt.904
Downsview, Ontario, M3H 4X7,
Canada.
tel. (416)-398-5947
e-mail: bk772@freenet.toronto.on.ca

From owner-ageing@net.bio.net Thu Jul 06 23:00:00 1995
Path: biosci!bcm!cs.utexas.edu!howland.reston.ans.net!europa.chnt.gtegsc.com!news.umbc.edu!haven.umd.edu!purdue!mozo.cc.purdue.edu!not-for-mail
From: barani@mace.cc.purdue.edu (Barani)
Newsgroups: bionet.molbio.ageing
Subject: AGEING of Cells vs Organisms
Date: 7 Jul 1995 11:26:39 -0500
Organization: Purdue University
Lines: 21
Message-ID: <3tjn7v$qmp@mace.cc.purdue.edu>
NNTP-Posting-Host: mace.cc.purdue.edu

   AGEING of an Organism is different from AGEING of individual 
   cells. Sometimes faster AGEING of cells may mean a slower 
   AGEING of the organism. For example, older cells should be 
   destroyed in an organism as fast as possible and replaced 
   with newer young cells. Otherwise older cells can lead to 
   cancer.  For the organism AGEING can be counted based on 
   markers that are breakdown-points in metabolic pathways. Some 
   critical breakdowns lead to visible changes in the organism
   like greying of hair.

   Barani
   Lilly Hall of Life Sciences
   Purdue University

	    |         |          |           |           |
	  -----     -----      -----       -----       -----
	    |         |          |           |           |
   ================================================================
   |  This box is dedicated to the memory of those who spent their|
   |  Lifetimes on the AGE-OLD problem of the OLD-AGE problem.    |
   ================================================================

From owner-ageing@net.bio.net Thu Jul 06 23:00:00 1995
Path: biosci!SINGER.ASRI.EDU!MANEV
From: MANEV@SINGER.ASRI.EDU
Newsgroups: bionet.molbio.ageing
Subject: REGISTRATION IS IN PROGRESS FOR APOPTOSIS SYMPOSIUM
Date: 7 Jul 1995 04:52:12 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 7
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.3.89.9507070707.A22681-0100000@SINGER.ASRI.EDU>
NNTP-Posting-Host: net.bio.net

International Symposium on Oxidative Stress, Apoptosis and Brain Damage
will be held in Pittsburgh, PA from September 21 to 24.
Registration is in progress ($ 250, three days; includes course materials,
welcome reception, continental breakfast, lunch and refreshment breaks 
each day).
For information please call: +412-359-4952.


From owner-ageing@net.bio.net Thu Jul 06 23:00:00 1995
Path: biosci!galaxy.ucr.edu!library.ucla.edu!agate!overload.lbl.gov!lll-winken.llnl.gov!enews.sgi.com!decwrl!waikato!auckland.ac.nz!kcbbs!planet!chambers!steve
From: steve@chambers.ak.planet.co.nz (Steve Chambers)
Newsgroups: bionet.molbio.ageing,sci.life-extension
Subject: Re: Needed:Information about aging and death of organisms (human, animals)
Message-ID: <Nqa-vAHPBh107h@chambers.ak.planet.co.nz>
Date: Fri, 7 Jul 95 17:43:41 +1200
References: <AC20DB9F966833A01@port15-highway.extern.uni-ulm.de>
Organization: PlaNet (Auckland New Zealand)
Lines: 80
Xref: biosci bionet.molbio.ageing:1846 sci.life-extension:6021

In <AC20DB9F966833A01@port15-highway.extern.uni-ulm.de> Anne.Lilie@extern.uni-ulm.de (Anne Lilie) writes:
>Hello,

Hi Anne

This is quite a shopping list of questions!  And I hope it'll stimulate 
some discussion for you.  I'll (I hope) start the ball rolling by 
answering them as succinctly as I can.


>-What exactly happens when an organism ages? 

It varies from organism to organism, and for each organism there are a
_huge_ number of changes associated with aging.

>Does the metabolism slow down,

Usually, but there's no reason for us to _assume_ that that's a bad thing.
Indeed, there are many reasons to think that a reduced metabolism may be
beneficial.

>and therefore reduces the intake of oxidation and water (which leads to
>hydration of the skin etc..)?
>-And why does the organism loose water (newborn 90% but adult 80%)?

I imaging that this is largely a function of increased fat %, rather than 
anything else.  However, connective tissue Xlinking and general conn. tiss.
disorder may be a factor.

>-Why do some people age later and some sooner? 

Variability in biological function is the norm - rather than the exception.

>Is the "aging clock" build in the cell?

There is certainly some form of clock in most cells which influences the
aging (or more correctly the cellular senescence) of those cells.  Whether
this has any influence on the aging of whole organisms has yet to be
determined.

>-Are all tissues (cells) affected? 

No - at least not significantly so within the lifetime of any multicellular
organisms that I'm aware of.

>Where (in which cells) does the aging process start? Or does it start 
>gradually? 

Aging is an amalgam of many processes.  Some of them start the moment a 
cell comes into existence.  

>Are only certain tissues affected?

Effects to only some tissues have so far been shown to influence age-
dependant mortality.  

>-During the aging process, how do the molecules react and in which way do
>they change their composition?

Aging processes are many and varied.  Some of the more important "molecule
changing" agents are; reactive oxygen species and other free radicals,
glycosylation and other crosslinking reactions.

>-What is death? During the aging process have the molecules changed
>gradually,  that in the end, they just cant react anymore or very little
>with each other, and then just start falling apart (causing the organism,
>to get less and less resistant to illness...)?

>Thank you, waiting for your answers,

I've crossposted this to bionet.molbio.ageing and sci.life.extension.  Check
these newsgroups out - these matters are discussed regularly there. 

Steve

-- 
 ________________________ 
(I_lurk,_therefore_I_am!_\  ,,,                           Steve Chambers
                           (o o)          steve@chambers.ak.planet.co.nz
-----------------------oOO--(_)--OOo------------------------------------

From owner-ageing@net.bio.net Thu Jul 06 23:00:00 1995
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!howland.reston.ans.net!usc!chandler.hsc.usc.edu!user
From: hutchin@hsc.usc.edu (Tim Hutchin)
Newsgroups: bionet.molbio.ageing
Subject: Re: Aging or Ageing?
Date: Fri, 07 Jul 1995 09:28:21 +0000
Organization: University of Southern California
Lines: 9
Sender: hutchin@chandler.hsc.usc.edu
Distribution: world
Message-ID: <hutchin-0707950928210001@chandler.hsc.usc.edu>
References: <3tjjt2$36k@ixnews7.ix.netcom.com>
NNTP-Posting-Host: chandler.hsc.usc.edu

In article <3tjjt2$36k@ixnews7.ix.netcom.com>, "Lawrence C. Chen"
<g2bfunky@ix.netcom.com> wrote:

> Isn't the correctly spelling "AGING"?

Only if you're American.  The correct English spelling is ageing.

-- 
                                             

From owner-ageing@net.bio.net Thu Jul 06 23:00:00 1995
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!howland.reston.ans.net!ix.netcom.com!netnews
From: "Lawrence C. Chen" <g2bfunky@ix.netcom.com>
Newsgroups: bionet.molbio.ageing
Subject: Aging or Ageing?
Date: 7 Jul 1995 15:29:38 GMT
Organization: Netcom
Lines: 2
Distribution: world
Message-ID: <3tjjt2$36k@ixnews7.ix.netcom.com>
NNTP-Posting-Host: ix-ir16-03.ix.netcom.com
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 1.2b2 (Windows; I; 16bit)

Isn't the correctly spelling "AGING"?


From owner-ageing@net.bio.net Fri Jul 07 23:00:00 1995
Path: biosci!bloom-beacon.mit.edu!news.starnet.net!wupost!waikato!auckland.ac.nz!kcbbs!planet!chambers!steve
From: steve@chambers.ak.planet.co.nz (Steve Chambers)
Newsgroups: bionet.molbio.ageing
Subject: >Aging or Ageing?
Message-ID: <lap-vAJFBh107h@chambers.ak.planet.co.nz>
Date: Sat, 8 Jul 95 10:31:01 +1200
References: <3tjjt2$36k@ixnews7.ix.netcom.com>
Organization: PlaNet (Auckland New Zealand)
Lines: 18

In <3tjjt2$36k@ixnews7.ix.netcom.com> "Lawrence C. Chen" <g2bfunky@ix.netcom.com> writes:
>Isn't the correctly spelling "AGING"?

Writers of English english tend to use "ageing" while those of American
english tend to use "aging".  Either is correct according to the Oxford
Dictionary.

I use "aging" because it's used five times more frequently in scientific
literature.  (Do a medline search using both and you'll see what I mean.)
Common usage is the mother of language.

Steve

-- 
 ________________________ 
(I_lurk,_therefore_I_am!_\  ,,,                           Steve Chambers
                           (o o)          steve@chambers.ak.planet.co.nz
-----------------------oOO--(_)--OOo------------------------------------

From owner-ageing@net.bio.net Fri Jul 07 23:00:00 1995
Path: biosci!POSSUM.MURDOCH.EDU.AU!cummins
From: cummins@POSSUM.MURDOCH.EDU.AU (Jim Cummins)
Newsgroups: bionet.molbio.ageing
Subject: Re: >Aging or Ageing?
Date: 7 Jul 1995 19:21:34 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 8
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.SUN.3.90.950708102457.13072E-100000@possum>
References: <lap-vAJFBh107h@chambers.ak.planet.co.nz>
NNTP-Posting-Host: net.bio.net

Who cars?

Dr Jim Cummins                            +61-9-360 2668
School of Veterinary Studies          FAX =61-9-310 4144     
Murdoch University               cummins@possum.murdoch.edu.au
Murdoch, Western Australia 6150
"For every complex problem there's a simple solution.  And it's wrong!"


From owner-ageing@net.bio.net Fri Jul 07 23:00:00 1995
Path: biosci!ns1.faseb.org!darwin.sura.net!www.uno.edu!uno.edu!KGPL
From: kgpl@uno.edu
Newsgroups: bionet.molbio.ageing
Subject: Free Radicals in Cell Nuclei?
Date: 8 Jul 1995 09:12:31 GMT
Organization: University of New Orleans
Lines: 10
Message-ID: <3tli5v$utc@www.uno.edu>
Reply-To: kgpl@uno.edu
NNTP-Posting-Host: jazz.ucc.uno.edu

Someone has suggested to me that a lot of age-related damage may
be the result of accidental miscopying of DNA due to the presence
of free-radicals in cell nuclei messing up the copying process.
Is this possible?  What kinds of free-radicals are generated within,
or can get into, the nucleus of a cell?  Is there any reason to
suspect that this sort of damage is more likely to occur during
the process of cell division?
 
Thanks,
Kevin

From owner-ageing@net.bio.net Fri Jul 07 23:00:00 1995
Path: biosci!biosci!not-for-mail
From: agerus95@glas.apc.org (Vitaly I. Dontsov)
Newsgroups: bionet.cellbiol,bionet.molbio.ageing
Subject: Information Bulletin of Foundation of Life prolongation
Date: 8 Jul 1995 08:31:38 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 888
Sender: kristoff@net.bio.net
Distribution: world
Message-ID: <m0sUUtD-0006zCN@glas.apc.org>
NNTP-Posting-Host: net.bio.net
Xref: biosci bionet.cellbiol:2536 bionet.molbio.ageing:1854

                  *******************************************
                  *                                         *
                  *      A G E  and  L O N G E V I T Y      *
                  *                                         *
                  *******************************************
                             INFORMATION BULLETIN
                     of FOUNDATION for LIFE PROLONGATION
                                   Vol.5
                                  MOSCOW
                            RUSSIAN FEDERATION

    E.MAIL: agerus95@glas.apc.org  ( in GlasNet )
    E.MAIL CONFERENCE: AGEING&LONGEVITY.BIOMED.NEWS(RUS)
                        in brief: ageing.biomed ( in GlasNet )
    Tel.(095) 903-16-40, 365-05-25( Foundation for life prolongation )
        (095) 903-16-40 ( Clinical consulting Center )
        (095) 365-03-25, 365-05-25 ( Scientific researches )
                        For correspondence:
          prof. Podkolzin A.A.,  D.M.,  Academician of New York
          Academy of Science,  Director of Central scientific  research
          laboratory, MOSCOW medical Stomatological Institute
          ( or Vitaly I.Dontsov, M.D. )
          Moscow, 103473,  Delegatskaja str.,  20.  Russian  Federation
          Fax.(095)  973-32-59  Tel.(095)  365-05-25, 365-03-25
 ---------------------------------------------------------------------------
                             - 2 -

    CONTENTS:

 About the Foundation for Life Prolongation .............................  3
 Programme of The first  Russian  conference  "Medical  and  biological
      aspects of normal and pathological aging"........................... 4
 Brief communications and thesises of  reports  of  The  first  Russian
      conference   "Medical   and  biological  aspects  of  normal  and
      pathological aging"................................................. 7
 Foundation of life prolongation present original scientific reports:.....19
 Foundation of life prolongation present original scientific projects:....21
 New complex scientific-research programme "New biological and physical
      methods in diagnostics and treatment of tumours"....................24

 ---------------------------------------------------------------------------
                             - 3 -

                     FOUNDATION for LIFE PROLONGATION

     Scientific non-state  organization,  which carry out coordination,
 realization and financing investigations in Biology of Aging  and Life
 Prolongation,  new  and  ancient  methods for creative realization and
 self-improvement  of  individuals,  new  methods  of   biostimulation,
 bioactivation and rejuvenation.
     Scientific researches from Russian Academy of Sciences, Academy of
 Medical  Sciences and Ministry of Health participates in our programs.
                           FUND CARRY OUT:
     Coordination of  complex investigation programs in fundamental and
 clinical assay in biology of aging and the life prolongation.
     Organization of conferences and meetings.
     Publicize books,  reports,  prepare computer programs.
     Leading scientists  in  Biology  of  Aging  and  Life Prolongation
 present lectures and reports.
     Organization of working-outs,  production and marketing of special
 devices and methods .
     Realization of East and Ancient health courses, which help to make
 creative realization and self-improvement of individuals.
  Accomplishing other measures in Biology of Aging and Life Prolongation.

    Tel.(095) 903-16-40, 365-05-25( Foundation for life prolongation )
        (095) 903-16-40 ( Clinical consulting Center )
        (095) 365-03-25, 365-05-25 ( Scientific researches )
                        For correspondence:
          prof. Podkolzin A.A.,  D.M.,  Academician of New York
          Academy of Science,  Director of Central scientific  research
          laboratory, MOSCOW medical Stomatological Institute
          ( or Vitaly I.Dontsov, M.D. )
          Moscow, 103473,  Delegatskaja str.,  20.  Russian  Federation
          Fax.(095)  973-32-59  Tel.(095)  365-05-25, 365-03-25

 ---------------------------------------------------------------------------
                            - 4 -
              INFORMATION of FOUNDATION for LIFE PROLONGATION
                   About:  THE FIRST RUSSIAN CONFERENCE
    "MEDICAL AND BIOLOGICAL ASPECTES OF NORMAL AND PATHOLOGICAL AGING"
                     ( 23-24 November, 1993, Moscow )
        Institute of chemical physic of Russian Academy of Science
      Moscow seciety of Nature researchers of Moscow State University
   Foundation for Life prolongation,  International association "FENIX"
  Central research laboratory of Moscow medical stomatologocal institute

               I SECTION:"FUNDAMENTAL MECHANISMS OF AGING".
  1.Surmounting of the species barier of human  lifestrategical problem
    of its radical prolongation. Vischev I.V., D.Ph.
  3.Fundamental mechanisms of aging,  it general types and  mechanisms.
      Dontsov V.I., M.D.
  4.The problems of aging and mortility of high  organisms  and  Darvin
    natural selection theory. Akifjev A.P., Ph.D.
  5.The nature of organism ageing process. Muhankin A.I., Ph.D.
  6.The systems of life longivity determination. Gubanov E.A.
  7.Humans manifests the potentially non-aging properties.Haljavkin A.V.
  8.Gene-immortalised effects   on  cell  mitosis  and  differentiation
    regulation,  aging and programmed cell wreck. Haljavkin A.V., Ph.D.
  9.DNA secondary structure defects,  recognited by S1 nuclease and its
    probable role in somatic mammalians cells aging.Potapenko A.I.,Ph.D.
  2.Mathematical model and whole graphic of age mortility, its probable
    physiological sense and new immunological theory of aging.Dontsov V.I.
 10.Epygenetic structurization  of  biosystems time and new forms of DNA
    memory. Garjaev P.P.,Ph.D.
 11.Wave mechanisms  of  gene  regulation  and  its  role  in  cell age
    correction. Chirckova E.N., Ph.D.
 12.Embrion hypothalamic transplantation as method of organism develop-
    ment programm correction. Ata-Muradova F.A.,Ph.D., Dontsov V.I.,MD
 13.About possible artificial life prolongation by"gene  cycling"  me-
    thods. Isaev N.N.
 14.Mathematical models of mortility graphics. Poltorakov A.P.
 15.Age-dependent mortility from leukosis:  effects  of  radiation  and
    age. Mamaeva E.F., Ph.D.
 16.The biological effects of age age-increasing mortility. Mamaev V.B.
 17.Biorhytmes as probable regulator mechanism of life term.Bakaev V.V.
 ---------------------------------------------------------------------------
                             - 5 -

   II SECTION: "CLINICAL AND PHYSIOLOGICAL RESEARCH AND BIOSTIMULATION".
  1.Theory, physico-chemical  and  biological  basis  of "agents of low
    intensivity" effects. Podkolzin A.A., M.D.
  2.Mechanisms of   "agents   of   low   intensivity"effect:  resonanse
    stimulation immune antibody production in mice by the  use  of  low
    intensivity pulse current. Barysheva A.V., M.D., etc.
  3.Immunomodulation effects  of  low  intensivity  magnetic  field  on
    immune antibody production in mice. Dontsov V.I., M.D.
  4.The new method of function and  bioenergetic  diagnosis,  treatment
    and   bostimulation  by  the  original  electroacupuncture  without
    external currents. Makaz V.G., M.D.
  5.Device and patented method of tumour diagnosis by spectrofluorescence.
    Makaz V.G., M.D.
  6.New properties  for  effects on free-radical mechanisms of aging by
    electrochemical ativated systems. Podkolzin A.A., M.D. etc.
  7.Genetics aspects of artificial life prolongation prolem. Borisov S.E.
  8.Analysis of some effective methods of life prolongation: hypobiosis
    as perspective method for life prolongation in mammalians.
    Chernilevsky V.E., Ph.D.
  9.About effects  of  some phyto-extracts on development and life term
    in plants. Aleutsky N.N.,M.D.
 10.New effective   phyto-microelement   and   homeopathic  complexes.
    Shepelenko A.M. etc.
 11.Adaptation as  method  for  regulation  of  aging  process in man.
    Muhankin A.I., Ph.D.
 12.About some indexes in the measuring of human aging rate.
    Verchotin M.A., Ph.D.
 13.The principle of minimum energy in ontogenesis and age bioenergetic
   problems. Ozernuk N.D.,Ph.D.
 14.About effects  of  age  on  activity  of  enzymes of lipids and DNA
    methabolism. Romanenko E.B.
 15.Neuro-phisiological aspects  in  the measuring of human aging rate.
    Novoselov V.M.
 16.Analysis of  energy-producing  systems  regulation  mechanisms  and
    methods for its measuring. Pospelov A.A., M.D.
 17.Some aspects  of  the  mathematical  models  of  human  aging  rate
    measuring. Zajarny A.N.
 ---------------------------------------------------------------------------
                             - 6 -
 18.Homeopathical profilaction  of aging. Sluzkin N.I.,M.D.
 19.About low temperature effects on life term of some vermics.Bakaev V.V.
 20.Depression in  age  and  problems  in  surmounting of resistance to
    remedies. Bujkov V.A., M.D.
 21.Selenium concepts  of  decreasing  man  supermortility  in Finland.
     Anuphriev A.D.
 22.New opportunities of weak bioelectrocurrents and non-ionizing radi-
    ation in diagnosis, treatments and age biostimulation. Dontsov V.I.

           III SECTION: HISTORY OF GERONTOLOGY, SOCIAL ASPECTS,
                        ANCIENT EAST METHODS OF LIFE PROLONGATION.
  1.Term of life and its secret.  Belova T.A., Ph.D.
  2.Life prolongation  as a science. Tuev  V.A., Ph.D.
  3.About creation   of   National   Institute   of   Health  and  Life
    Prolongation. Vishev I.V., Ph.D.
  4.About centers of life prolongation.Ananjev V.M,Ph.D.
  5.The working expirience of  life  prolongation  center  "Anastasis".
    Bogolubova L.G., Ph.D., etc.
  6.Mathematical models of effects of social and psychical  factors  on
    human aging. Judasin L.A.
  7.Psychotherapy as prophylactic  factor  on  patients  with  cerebral
    atherosclerosis. Grigorjevskich V.S.,MD
  8.Energy self-organization in cell and energy interaction in organism.
    Fofanov S.I.
  9.General methodology of East and Ancient esoteric ( secret ) knowledge
    and psychotechnics. Dontsov V.I., MD
 ---------------------------------------------------------------------------
                             - 7 -
 BRIEF COMMUNICATIONS AND THESISES OF REPORTS of THE FIRST RUSSIAN CONFERENCE
     "MEDICAL AND BIOLOGICAL ASPECTS OF NORMAL AND PATHOLOGICAL AGING"

                      FUNDAMENTAL MECHANISMS OF AGING

                FUNDAMENTAL MECHANISMS AND TYPES OF AGING.
                             Dontsov V.I., MD
   Central scientific research laboratory, MOSCOW medical Stomatological
    Institute. Moscow,103473, Delegatskaja str.,20. Russian Federation
            Fax. (095) 973-32-59 Tel.(095) 365-03-25, 365-05-25

    Original theoretic  and  experimental  reports  about  the computer
 models of sells-renovation processes in  mammalians,  which  can  make
 possible obtaining the whole graphic of age mortality and to speculate
 about probable physiological sense of it.  Theoretical presentation of
 4 principal ,  general types of aging and special role of the critical
 part for mammalians  aging  mechanism  -  reduction  of  self  tissues
 renovation;  special models of its regulation mechanisms in mammalians
 and humans especially.
    Here is  completely new lymphoid theory of aging,  based on the new
 lymphocytes function - its ability to  regulate  growth  of  different
 cell types. Theoretical, mathematical models, special bibliography and
 original experimental studies illustrate:  regeneration  of  different
 tissue  and  specially  lymphocyte function decline with age,  what is
 equivalent to the reduction of cells renovation.
    The commercial  products for research,  education and advertisement
 may be elaborated.
 ---------------------------------------------------------------------------
                             - 8 -
  MATHEMATICAL MODEL WHICH MAKE IT POSSIBLE TO OBTAIN THE  WHOLE DIAGRAM
          OF AGE MORTALITY AND ITS PROBABLE PHYSIOLOGICAL SENSE.
                             Dontsov V.I., MD

    The general cybernetic point of view on the biological systems have
 shown  two principle mechanisms of its structure (state) steadfastness
 during the time:  a) by the formation of nonregenerated units ( teeth,
 nefrons,  nerve  cells,  non-reparated  DNA  sites etc.  ),
    b) by the dynamic balance of self-renovated units (  metabolism  of
 biomolecules,  cell  regeneration  of  skin,  liver and other internal
 organs, regeneration of some tissues and organs etc. ).
    The non-regenerated   units   existence  in  mammalians  and  other
 contemporary intricated organisms  is  the  result  of  some  impotent
 special processes ( for example, the information storage in mind or in
 DNA-genes ) and the result of high natural animal mortality  when  the
 age period of life have not any evolution significance.
    These situation leads to the  fundamental  mechanism  of  age:  the
 numbers  decreasing during time of the non-renovated molecules, cells,
 organs etc.(  because  of  limiting  existence  probability  of  every
 separate  units  ) and increasing of mutants units with low functional
 power ( because for more probable unfavorable results of mutation ).
    For self-renovated    units    3    principle    processes   exist:
 1)self-regeneration (metabolism,  cell  mitosis,  tissue  regeneration
 etc.), 2)fatal case for some units ( and elimination from system ) and
 3)mutation of some units ( without  elimination  from  system  but  it
 leads to decreasing of system effectiveness ).
 ---------------------------------------------------------------------------
                             - 9 -
    The mathematical  model  of  these processes is:
    dA/dt = c*A/(c1*A + c2 ) - k1*A - k2*A
    dmA/dt = c3*mA/(c4*mA + c5) - k3*mA + k2*A
 where A  and  mA  -  the  number  of  normal  and  mutant units,  that
 self-renovation is depended on self-number ( the positive  feedback  )
 and  is limited with self-number ( the negative feedback,  for example
 chalone mechanism ). The number decreasing of normal units is depended
 on its fatal cases and mutation, for mutated units - only fatal cases.
 "C" and "k" are coefficients that may vary due to balance  of deferent
 regulator  factors  of  organism,  that  leads  to  dynamic balance of
 self-renovated systems.
    Everybody can  see by use the computer models the self-formation of
 dynamic balance of self  -renovated  system  that  is  described  with
 formula  1  and time-depended elimination of non-renovated units.  The
 necessary terms for balance are k1 < k3 ( normal units  must  be  more
 steady  than mutants that is realistic ).  System is unsteady to tumor
 growth (negative feedback lack ), but it is not mechanism of aging.
    As result   of   co-existence   of  renovated  and  not  units  its
 interactions exist also. If regeneration level of self-renovated units
 is  depended  on  non-renovated  units  number,  the age-period during
 ontogenesis must be exist.  The cause of this  situation  may  be  the
 processes of organism growth and its limitations during ontogenesis.
    The mammalians  mechanisms  of  reproduction  needs  in  period  of
 organism  growth  and  in its limitation mechanisms due to gravitation
 barrier and food-dependence of growth.  As self-renovation  may  exist
 without general mass growth, not general growth limitation mechanisms,
 but  special  TYPE  of  growth  limitation  leads  to  age  period  in
 mammalians.  It  is  clear that self-renovation mechanism have not any
 internal tendency both growth and degradation  but  only  for  dynamic
 balance   in   time.   The   result  of  renovatednon-renovated  units
 interaction, unlikely, have these time-depended mechanisms.
 ---------------------------------------------------------------------------
                             - 10 -
    We propose the next general theory of growth regulation in organism
 with period  of  aging.  Let  level  of  renovation  in  multicellular
 organism  ( and general organism mass as its function ) be depended on
 concentration of some stimulated renovation (  for  example  enhancing
 coefficient  "c"  in  formula  1 ) factor "F" - the product of special
 positive regulator cells "D".  For time-depended  growth  during  some
 years  it is necessary the positive F-factor gradient.  The well-known
 biological mechanism for this situation realization  is time-dependent
 natural  death of negative regulator cells "I":  the balance D - I = F
 is resulting in stimulation of growth or its restriction. If "D" cells
 is  renovated,  growth is limited but there is no any period of system
 degradation   (   period   of   aging);   if   the   "D"   cells    is
 non-renovated,there  is period of aging as result of decreasing of "D"
 cells number due to formula 2:
    dD/dt = - Kd*D , dI/dt = -Ki*I ,( Kd < Ki).
    The general  curve  of  time-depended  renovation  change  and  its
 depended  age  mortality  have  shown  on Fig.1.  The age mortality is
 presented as log ( 1/F ) due to general theory of aging  as decreasing
 of "general vitality" ( as function of "F" ).
    Anyone may see the well coincidence of theoretical  curve  and  any
 experimental  and demographic real age mortality curves.  This results
 is coincident with regulator group theory of aging and show  the  main
 mechanism  of  aging - the decreasing of renovation level of different
 regenerated units in organism.
    The results   of  its  is  mass  decreasing  during  the  age,  the
 increasing of time,  needs  for  renovation  of  deferent  regenerated
 units,  the  increasing  of  mutants  units  and  other all well known
 symptoms of age.  The  specific  morphological  substrates  may  be  -
 regulator non-renovated cells of hypothalamus, deferent growth factors
 in  blood;  for  peripheral  mechanisms  -  proliferated   cells   and
 mechanisms of its regulation,  especially,  some types of lymphocytes,
 that regulate proliferation  of  somatic  cells.  We  have  shown  the
 existence  of special lymphoid system,  that regulate proliferation of
 all cell type in organism and proposed special theory of aging as time
 -dependent  decrease in lymphoid-regulation of somatic cell renovation
 ( Dontsov V.I.,  1990,  1993 ).  The thymus-dependent hypophys-induced
 degradation may be reversed,  with restoration of growth, reproduction
 and some other symptoms of  age  by  deferent  methods,  for  example,
 embryo  hypothalamic  transplantation ( Ata-Muradova F.A.  et al.1987;
 Matsumoto A.et al.,1984 ).
 ---------------------------------------------------------------------------
   p  o                     - 11 -                    o     o     o
   a                                          o
   r   o                                o             Ln M
   a                                o
   m    o                         o
   e                            o
   t     o                    o
   e                        o
   r      o               o
   s                    o
  100- . *  o          o
       .   *        o
        .  o  *   o
         .  o + o*
          . + o  +    *
          +.          +    * +
         +   .                   * +
        +      .                       +*
       +F         .                              +*
      +                .  I                                 +*  D
      ------------------------.----------------------------------------
    Figure 1.                                              300   Time
 The general  theoretical  curve of time-depended renovation change and
 its depended age mortality in  system,  that  contains  renovated  and
 regulatory non-renovated units.
    D -  stimulator  growth  regulator  cells,  I  -  inhibitor  growth
 regulator  cells,  F  =  D  -  I,  M - age mortality M = Ln(1/F) ( For
 D=I=100, Kd=0.01, Ki=0.05, c=10, M=Ln(1/(F+c)*100) * 100 )

    Reference.
  Ata-Muradova F.A.,  Dontsov V.I.  Proc.  Academy of Science of  USSR,
 1987.Vol.297,N.1.P.237-240 (Rus.).
  Dontsov V.I.  The immunobiology  of  postnatal  development.  MOSCOW.
 Science. 1990. 152 p.( Rus.).
  Dontsov V.I.  Age deficit of lymphocytes-regulator of  somatic  cells
 growth  as  probable  central  mechanism  of aging in mammalians.  In:
 "Aging and  longevity".  Ed.of  Fund   of   longevity.   Moscow,1993.
 N 1.P.18(Rus).
  Matsumoto A.et al.Proc.Japan Acap.,1984.Vol.60. Ser.B.N 4.P.73-76.
 ---------------------------------------------------------------------------
                             - 12 -
  LYMPHOCYTES-REGULATORS OF  CELL  PROLIFERATION  SHORTAGE  AS  POSSIBLE
                  CENTRAL MECHANISM OF MAMMALIANS AGING.
                             Dontsov V.I., MD.

    It is known that one of the central mechanism of  mammalians  aging
 is  the  age-dependent  decrease of tissues proliferous potential that
 leads to decrease of tissues and organs self-renovation.  The  general
 decrease of age cell mitotic index affects all cell types and increase
 the cell share in G1 phase of cell cycle which is coincided to  be the
 result  of  the well-known age cell G1/S block,  the cause of which is
 unknown.
    Immunology considers  the  analogous  G1/S  block  of  age  animals
 lymphocytes which  proves  to  be  the  result  of  T-cells  regulator
 populations:  during  age there is increase of T-suppressers share and
 decrease in  T-helpers  which  results  from  hypothalamic-lymphocytes
 effects on the thymus in age.
    It has been shown that lymphocytes  are  capable  of  regulation  a
 number  of  non-immune function in organism.  Lymphocytes transfer the
 "regeneration information"  to  normal  animals  which  increases  the
 normal recipientts liver,  kidney and other organs and tissues mitotic
 index  in  10  or  even  100-times;  lymphocytes  also  take  part  in
 physiological self-renovation of proliferous cells containing tissues,
 in tissues hyperplastic processes, malignant cells growth, in organism
 growth  and its restriction in age adults,in regulation of homeopathic
 cells differentiation and growth processes and other  functions  where
 cell  proliferation  and  growth  are  the  central  physiological  or
 pathogenic  mechanism  (  Babaeva,  1982;  Prehn,1972;  Rosenfeld   et
 al.,1977; Wortis,1974 etc.).
    All these data severed the basis for our hypothesis that lymphocyte
 system  of  organisms has been primarily formed not only for immunity,
 but  for  regulation  of  all  cell  growth  processes   types   which
 biologically are most impotent in all types of multicelular organisms.
 ---------------------------------------------------------------------------
                             - 13 -
    In fact,  the decrease of this  lymphocytes  function  may  be  the
 central   mechanism   of   aging,  especially  for  proliferous  cells
 containing tissues.  The author has elaborated the theory  of  special
 lymphoid  system  in  multicellular  organisms regulating all types of
 cell proliferation and growth.
    Its elements   are   cell-proliferation-regulator   lymphocytes  of
 stimulator or inhibitor types ( CPL+  and  CPL-  ).  The  mathematical
 model  have  been created and CPL-dependent age-theory has been worked
 out ( Dontsov,1990,1993 ).
    The theory  has the following postulates:  1) The main mechanism of
 tissue and whole organism  age  process  is  decreasing  of  its  cell
 self-renovation.
    2) It is the result of disballance in CPL-system of organism.
    3) There  is decrease of CPL/+/ share in age mammalians accompanied
 by the general decrease of CPL.
    4) It  brings  to G1/S block both lymphocytes-effectors of immunity
 and proliferated somatic cells of all tissue types.
    5) As a result, there is decrease in tissue renovation and increase
 in life time (duration) of individual  low  proliferated  cells  which
 enhances the share of low proliferated cells in tissues.
    6) As tissue renovation mechanisms do not stop  but  only  decrease
 there  are  always  young  cells  present  in  age  tissues as well as
 compensatory hyperplastic processes etc.
    7) The disballance of CPL-system is the result of continued effects
 of  the  special  central  mechanism  regulating  the  restriction  of
 organism   growth   in   the   period  when  growth  is  stopped.  The
 morphological substrate  of  this  mechanism  is  hypothalamic  growth
 regulator centers ( Ata-Muradova et al.,1987 ).
 ---------------------------------------------------------------------------
                             - 14 -
    This theory being not contradictory but going along the  same lines
 with the basis theories of age, it show the principal mechanism of age
 realization  for   self-regenerated   tissues   in   connection   with
 fundamental  for  all mammalians process - growth and its restriction.
 The effects on non-proliferated cell-types may also be described.
    References.
  Ata-Muradova F.A.,  Dontsov V.I.  Proc.  Academy of Science of  USSR,
 1987.Vol.297,N.1.P.237-240 ( Rus.).
  Babaeva A,G.,Nesterenko V.G.,Judina  N.V.//Bulletin  of  experimental
 biology and medicine.1982.N.6.P.98 (Rus).
  Dontsov V.I.  The immunobiology  of  postnatal  development.  Moscow.
 Science. 1990. 152 p.( Rus.).
  Dontsov V.I.  Age deficit of lymphocytes-regulator of  somatic  cells
 growth  as  probable central mechanism of aging in mammalians// In:  "
 Aging  and  longevity".  Edition  of  Fund   of   longevity.   Moscow.
 1993.P.18(Rus.).
  Prehn R.T.//Science.1972.Vol.176.P.170-171.
  Rosenfeld R.,Thorsson A.V.,Hintz R.J. Clin.Endocrinol.and Methabol.
    1977.Vol.48.P.456-461.
  Wortis H.//Contemp.Top.Immunobiol.,1974.Vol.3,P.243.

 PHYSICO-CHEMICAL AND BIOLOGICAL BASIS OF WEAK INTENSITY FACTORS EFFECTS.
             Podkolzin A.A.,MD, Dontsov V.I.,MD, Makaz V.G.,MD

    Physico-chemical and biological basis of high response of organisms
 to  weak  intensity  factors  ( low electric and magnetic fields,  low
 currents,  low doses of chemicals etc.) effects has been analyzed. The
 next specific mechanisms of this type effects are proposed: effects on
 different types of biomolecules oscillation,  resonance  of  different
 cells  structures,  energy  transformation  from  one type to another,
 effects on calcium ions activity etc.  It has been shown the formation
 of  the self-organization and hierarchic self-controlling processes in
 organism.
    The resonance  mechanism  may  be  the  basis  mechanism  for  weak
 intensity factor effects, especially for physical ones.
    The safety   and  high  effective  methods  for  treatment  may  be
 elaborated on the basis of weak intensity factor effects.
 ---------------------------------------------------------------------------
                             - 15 -

 THE RESONANCE EFFECTS OF WEAK AC/DC MAGNETIC FIELD ON IMMUNNITY IN MICE.
    Podkolzin A.A.,MD,  Dontsov  V.I.,MD,  Poponin  V.P.,Ph.D.
  Central Scientific Research Laboratory of Moscow Medical Stomatological
    Institute, Lebedev Institute of Physics Russian Academy of Science.

    In present  contribution  activated by antigen immune cells of mice
 was used as test system in order to verify concept,  that  weak  DC/AC
 magnetic  field tuned on calcium resonance may influence on calmodulin
 dependent signal trunsduction pathways in cells.  It  has  been  shown
 previously  [1],  that  for  this  mechanism  to  be  effective  it is
 necessary that calcium  bound  within  protein  be  in  nonequilibrium
 state. It is naturally to make assumption that nonequilibrium state of
 bound calcium is realized in activated  cells.  Plaque  forming  cells
 (PFC)   from   mice   spleen  were  prepared  on  the  4th  day  after
 immunization.  The  erythrocytes  of  rats  were  used  as   antigens.
 Measurement  of  the  antibody  rate productivity was made by standard
 Canningham A.[2].  It was simple procedure of counting the  number  of
 plaques in the sample (special chambers).
    In the case then horizontal  component  of  Geomagnetic  field  was
 compensated  sharp  resonance increase of antibody production activity
 was observed.  Resonance was observed in the region of 15 to 60 Hz the
 resonance  frequency  depend  on the value of vertical component of DC
 magnetic field.  The width of resonance was 0.3 Hz and quality was  in
 the range from 3 to 10.  This results are interpreted in the framework
 of calcium octahedron complex concepts [1].
    References
  Poponin V.P.  Possible  general  primary  mechanism  for  low   power
 nonionizing  radiation bioeffects.  Transactions of the First Congress
 of The European Bioelectromagnetics Association,  January 23-25, 1992,
 Brussels, Belgium, p.6.
  Canningham A.J.  A method  of  increased  sensitivity  for  detecting
 single antibody-forming cells// Nature.1965.Vol.207.P.1106-1107.
 ---------------------------------------------------------------------------
                             - 16 -
          THE CLOSE-RESONANCE  STIMULATION  OF  IMMUNITY IN MICE
                         WITH WEAK PULSE CURRENT.
                   Dontsov V.I.,M.D., Podkolzin A.A., MD

    The special  feature  of  weak  pulse  current  effects  on  immune
 antibody formation to rat erythrocytes has been  investigated.  Plaque
 forming  cells  (PFC) from mice spleen were registered on the 4-th day
 after immunization.  The erythrocytes of rats were used  as  antigens.
 Measurement  of  the  antibody  rate productivity was made by standard
 Canningham A.  method [1].  It was simple  and  precise  procedure  of
 counting  the  number  of activated specific antibody-producing immune
 cells in the parallel triplicate sample in special chambers.
    It was  fount  the  2-10 time Immunomodulation of PFC-generation in
 mice spleen 4 days after  immunization  on  5-10  minutes  weak  pulse
 current effects during 1 hour after immunization for immunostimulation
 and 4 hour after immunization for immunosupression.  The parameters of
 signal  was:  543  +1 kHz frequency and triangular or quadratic signal
 form,  that is typical for resonance  mechanism  effect  of  different
 stimulus.
   This results are interpreted in the framework of  calcium octahedron
 complex  concepts  as possible general primary mechanism for low power
 nonionizing radiation bioeffects and in general weak  intensity factor
 effects [2].
    The resonance  mechanism  may  be  the  basis  mechanism  for  weak
 intensity factor effects, especially for physical ones.
    The safety  and  high  effective  methods  for  treatment  may   be
 elaborated on the basis of weak intensity factor effects.
    References
  Canningham A.J. Nature.1965.Vol.207.P.1106-1107.
  Poponin V.P.  Transactions of the  First  Congress  of  The  European
 Bioelectromagnetics   Association,   January  23-25,  1992,  Brussels,
  Belgium, p.6.
 ---------------------------------------------------------------------------
                             - 17 -
   NEW METHOD OF FUNCTIONAL AND  BIOENERGETIC DIAGNOSIS,TREATMENT AND
 BIOSTIMULATION BY ORIGINAL ELECTROACUPUNCTURE WITHOUT EXTERNAL CURRENTS.
            Makaz V.G., MD Medical institute, Viniza, Ukraine.

    The method is works out and devices for  electroacupuncture without
 external  current are being produced.  The principle distinction of it
 in contrast to all methods of electroacupuncture is in that  that  not
 the outside imposing of electric rhythms in used,  but the stimulation
 of self activity of acupuncture points  that  allows  to  use  minimum
 currents and conduct minute side effects.
    The unique results are ached while treating burns of large surface,
 quick anti-burn complications ( intestinal paresis etc.  ),  treatment
 of pneumonia by non-injective method,  acceleration of different types
 reabilitaion processes etc.
    The special application for  reactivating  physiological  state  of
 tissues,  organs  and  whole  organism during age by this methods have
 shown in Institute of gerontology ( Kiev ) the unique results.
    The frequency-amplitude analyses of signals from acupuncture points
 are worked out that allows to receive new information about  the state
 of acupuncture points, internal organs, especially in age processes.

  DEVICE AND  PATENTED METHOD OF TUMOR DIAGNOSIS BY SPECTROFLUORESCENCE.
             Makaz V.G.,MD Medical institute, Viniza, Ukraine.

    On the  basis  of  original  self  theoretical   and   experimental
 researches  about  the lymphoid control of different cells types,  and
 especially tumors cell,  growth the new theory of lymphoid  mechanisms
 of  cancer  growth  has  been elaborated and new methods of its growth
 control have been shown.
    The new  method  of  tumor risk diagnosis by the use of biophysical
 resonance-interference method ( that make it  possible  to  accumulate
 specific  cancer  protein  signals  of  small  intensity  against  the
 background of considerable noise ) research of cancer  patients  serum
 fluorescence spectra was also elaborated, tested and patented.
    Common specific,  independent  of  the  tumor  nature  changes   in
 fluorescence  spectra were fount in double bland test on 200 different
 cancer patients and 200 controls with trustworthiness over 96% .
 ---------------------------------------------------------------------------
                             - 18 -

       NEW OPPORTUNITIES OF WEAK BIOELECTROCURRENTS AND NON-IONIZING
        RADIATION IN DIAGNOSIS, TREATMENTS AND AGE BIOSTIMULATION.
                             Dontsov V.I., MD

    We carry out  fundamental  theoretical  experimental  and  clinical
 works  on  studying  mechanisms of medical effect of weak currents and
 non-ionizing radiation, including the level of natural background.
    At first   calmodulin-   and   calcium-   dependent  mechanisms  of
 realization of such  effects  was  shown.  We  fount  out  the  narrow
 resonance stripes for biological effects and for the diagnosis aims by
 registration biocurrents,  studying  the  influence  of  magnetic  and
 electric fields on cells in isolated cells and whole organism.
    Immunostimulating, adaptogenic regimes are found out by using weak,
 principally harmful currents and physical fields.
    We designed devices ( apparatus BEST-1 ) for  immunostimulation and
 treatment, for example influence, on our theoretical basis.

     NEW PROPERTIES FOR EFFECTS ON FREE-RADICAL MECHANISMS OF AGING BY
                    ELECTROCHEMICAL ACTIVATED SYSTEMS.
                            Podkolzin A.A., MD

    According to the modern notions, oxidizing-reduction homeostasis is
 central  in  stability  of  organism  from  intoxication  and   radial
 affection.  The  free  radical-mechanism theory is also central modern
 theory of aging.  Anti-age stimulation mechanisms needs in principally
 harmful  agents  that  may be used for long time.  All types of modern
 anti-oxidants  remedies,  unfortunately,  are  very  toxic   and   its
 life-prolongation effects could not be used in humans for a long time.
    We investigated the EAS methods for preparation principally harmful
 agents  form  the water or weak solvent that may be used even in 1-2 L
 per day during many years.  Apparatus and regimes are  elaborated  and
 patented.  The method was tested for burns treating, immunostimulation
 and  bioenergostimulation.  The  possibilities   for   correction   of
 energetic  state  of  age organisms is discussed,  as the using EAS as
 radioprotection etc.
 ---------------------------------------------------------------------------
                             - 19 -
   FOUNDATION of LIFE PROLONGATION PRESENT ORIGINAL SCIENTIFIC REPORTS:

 1.THE LYMPHOID  MECHANISMS  OF   DIFFERENT   CELL   GROWTH   PROCESSES
   REGULATION IN MAMMALIANS:NEW IMMUNE THEORY of AGING.
   On the basis of monography:  Vitaly I. Dontsov "Immunobiology of the
 postnatal development". Academic Press"Science".Moscow,1990.
    Monography is  dedicated   to   new   lymphocytes   function:   its
 possibility  to  regulate  growth of different cell type.  Theoretical
 mathematical models,  special bibliography and  original  experimental
 studies  illustrate as some,  special,  type of T-lymphocytes regulate
 regeneration,  normal and tumor  growth,  immunity,self  physiological
 regeneration  of  different  tissue and specially as reduction of this
 lymphocyte function result in  age  -  reduction  of  cell  renovation
 (physiological  tissue self regeneration - the main mechanism of age).
    It is described the  lymphocytes  phenotype,  process  dynamic  and
 molecular mechanisms of this lymphocyte type activation and mechanisms
 of its effects on tissues.
    The elaboration  of the special computer models of this lymphocytes
 function make it possible the concreteness  for  different  physiology
 and pathology statements,  particularly the New Lymphoid Theory of Age
 model has been elaborated.

 2.FUNDAMENTAL MECHANISMS AND AGING TYPES.
   Original theoretic  and  experimental  reports  about  the  computer
 models  of  sell-renovation  processes  in  mammalians,  that  may  it
 possible to obtain the whole graphic of age mortality and to speculate
 about probable physiological sense of it.  Theoretical presentation of
 4  principal  general  types of aging and special role of the critical
 for mammalians aging mechanismreduction of  self  tissues  renovation;
 special  models  of its regulation mechanisms in mammalians and humans
 especially.
    The principal  new  lymphoid  theory  of  aging,  based  on the new
 lymphocytes function - its possibility to regulate growth of different
 cell type.  Theoretical mathematical models,  special bibliography and
 original experimental studies illustrate the mathematical mo  dels  of
 self  physiological  regeneration of different tissue and specially as
 reduction of this lymphocyte function result in  age  -  reduction  of
 cell renovation.
 ---------------------------------------------------------------------------
                             - 20 -

 3.NEW LYMPHOID  CONTROL  MECHANISMS  OF  TUMORS  GROWTH AND NEW DIVICE
   METHOD OF TUMOR AND TUMOR RISK DIAGNOSIS.
    On the   basis   of  original  self  theoretical  and  experimental
 researches about the lymphoid control of different  cells  types,  and
 especially  tumors cell,  growth the new theory of lymphoid mechanisms
 of cancer growth has been elaborated and new  methods  of  its  growth
 control have been shown.
    The new method of tumor risk diagnosis by the  use  of  biophysical
 resonance-interference  method  (  that make it possible to accumulate
 specific  cancer  protein  signals  of  small  intensity  against  the
 background  of  considerable noise ) research of cancer patients serum
 fluorescence spectra was also elaborated, tested and patented.
    Common specific,   independent  of  the  tumor  nature  changes  in
 fluorescence spectra were fount in double bland test on  200 different
 cancer patients and 200 controls with trustworthiness over 96% .

 4.NEW OPPORTUNITIES OF WEAK BIOELECTROCURRENTS AND NON-IONIZING
   RADIATION IN DIAGNOSIS,TREATMENTS,BIOSTIMULATION.
    We carry  out  fundamental  theoretical  experimental  and clinical
 works on studying mechanisms of medical effect of  weak  currents  and
 non-ionizing radiation, including the level of natural background.
    At first  calmodulin-  and   calcium-   dependent   mechanisms   of
 realization  of  such  effects  was  shown.  We  fount  out the narrow
 resonance stripes for biological effects and for the diagnosis aims by
 registration  biocurrents,  studying  the  influence  of  magnetic and
 electric fields on cells in isolated cells and whole organism.
    Immunostimulating, adaptogenic regimes are fount out by using weak,
 principally harmful currents and physical fields.
    We designed devices ( apparatus BEST-1 ) for im munostimulation and
 treatment, for example influence, on our theoretical basis.
    The unique results are ached while treating burns of large surface,
 quick anti-burn complications ( intestinal paresis etc.  ),  treatment
 of pneumonia by non-injective method,  acceleration of different types
 reabilitaion processes etc.
    The special  application  for  reactivating  physiological state of
 tissues,  organs and whole organism during age by  this  methods  have
 shown in Institute of gerontology ( Kiev ) the unique results.
 ---------------------------------------------------------------------------
                             - 21 -

 5.NEW POSSIBILITIES  FOR  CORRECTION OF ENERGETIC STATE OF ORGANISM BY
   ELECTROACTIVATED SYSTEMS.
    According to the modern notions, oxidizing-reduction homeostasis is
 central  in  stability  of  organism  from  intoxication  and   radial
 affection.  The  free  radical-mechanism theory is also central modern
 theory of aging.  Anti-age stimulation mechanisms needs in principally
 harmful  agents  that  may be used for long time.  All types of modern
 anti-oxidants  remedies,  unfortunately,  are  very  toxic   and   its
 life-prolongation effects could not be used in humans for a long time.
    We investigated the EAS methods for preparation principally harmful
 agents  form  the water or weak solvent that may be used even in 1-2 L
 per day during many years.  Apparatus and regimes are  elaborated  and
 patented.  The method was tested for burns treating, immunostimulation
 and  bioenergostimulation.  The  possibilities   for   correction   of
 energetic  state  of  age organisms is discussed,  as the using EAS as
 radioprotection etc.

   FOUNDATION of LIFE PROLONGATION PRESENT ORIGINAL SCIENTIFIC PROJECTS:

 1.THE EXPERIMENTAL RESEARCH OF RESTORATION GROWTH POTENTIAL OF
          DIFFERENT TISSUES IN AGE BY IMMUNOMODULATORS.
    MAIN IDEA:  To show the possibility and regimes of immunomodulators
 application  for  restoration  of  different tissues growth potential,
 based on original experiments and theory of special  type  lymphocytes
 function - regulation of non-immune cells growth.

 ---------------------------------------------------------------------------
                             - 22 -
 2.THE EXPERIMENTAL RESEARCH OF DEPRESSION GROWTH POTENTIAL OF
      DIFFERENT TUMOR TISSUES BY IMMUNOMODULATORS.
    MAIN IDEA:  To show the possibility and regimes of immunomodulators
 application for depression different tumor tissues  growth  potential,
 based  on  original experiments and theory of special type lymphocytes
 function - regulation of non-immune cells growth.

 3.THE EXPERIMENTAL RESTORATION OF THE ORGANISM-DEVELOPMENT PROGRAM BY
        EMBRIO HYPOTHALAMIC CENTERS TRANSPLANTATION.
    MAIN IDEA:  To  show  the  possibility  of  life-prolongation   and
 age-linked  function  restoration by methods of "Tissues engineering":
 transplantation  to  the  old  animal  brain  embryonic   hypothalamic
 centers.
    First experiments has shown the effectiveness of  this  method  for
 restoration  of  growth  rate,  stop  age  body  and organs mass loss,
 restoration immune function,  electroencephalografy-  and  test-memory
 function.

 4.NEW THEORETICAL MODEL OF LYMPHOID REGULATION OF CELL GROWTH
       PROCESS IN ORGANISM AND NEW THEORY OF AGE.
   MAIN IDEA:  The  elaboration  of  the special computer models of new
 lymphocytes function and concreteness of the  processes  of  different
 cell  growth  regulation by special types of lymphocytes for different
 physiology and pathology statements,  particularly  the  New  Lymphoid
 Theory of Age model may been elaborated.
    The commercial products for research,  education and  advertisement
 may be elaborated.
    On the basis of monography:  Vitaly I.Dontsov"Immunobiology of  the
 postnatal development". Academic Press"Science".Moscow,1990.
    Monography is  dedicated  to  new  lymphocytes   function   -   its
 possibility  to  regulate  growth  of  different cell type.Theoretical
 mathematical models,  special bibliography and  original  experimental
 studies  should  illustrate  as some,  special,  type of T-lymphocytes
 regulate  regeneration,  normal  and  tumor  growth,  immunity,   self
 physiological  regeneration  of  different  tissue  and  specially  as
 reduction of this lymphocyte function result in  age  -  reduction  of
 cell  renovation  (physiological  tissue  self regeneration - the main
 mechanism of age).
 ---------------------------------------------------------------------------
                             - 23 -
                          THE CLINICAL RESEARCHES

 A.THE FUNDAMENTAL RESEARCHES AND CLINICAL APPLICATION OF ORIGINAL
   ELECTROACUPUNCTURE WITHOUT EXTERNAL CURRENTS.
   MAIN IDEA: To show that new method of electroacupuncture do not only
 activate  different  function,  depressed  in age,  but also effect on
 Biological Age indexes.
    The principle  distinction  of  new  electroacupuncture stimulation
 method in contrast to all methods of  electroacupuncture  is  in  that
 that  not  the  outside imposing of electric rhythms in used,  but the
 stimulation of self activity of acupuncture points,that allows  to use
 minimum currents and conduct minute side effects.
    The first special application for reactivating  physiological state
 of tissues,  organs and whole organism during age by this methods have
 shown in Institute of gerontology ( Kiev ) the unique results.

 B.NEW OPPORTUNITIES OF WEAK BIOELECTROCURRENTS AND NON-IONIZING
        RADIATION IN AGE BIOSTIMULATION.
    MAIN IDEA:To show that new method of bioelectroimmunostimulation do
 not  only  activate  different functions,  depressed in age,  but also
 effect on Biological Age indexes.
    We carry  out  fundamental  theoretical  experimental  and clinical
 works on studying mechanisms of medical effect of  weak  currents  and
 non-ionizing radiation, including the level of natural background.
    Immunostimulating, adaptogenic regimes are fount out by using weak,
 principally harmful currents and physical fields.
    We designed devices ( apparatus BEST-1 ) for  immunostimulation and
 treatment, for example influen

 ---------------------------------------------------------------------------
                             - 24 -
  C.NEW POSSIBILITIES  FOR CORRECTION OF ENERGETIC STATE OF ORGANISM BY
                ELECTROACTIVATED SYSTEMS ( EAS ).
    MAIN IDEA:  To  show  that new method activate different functions,
 depressed in age, and effect on Biological Age indexes.
    The free  radical  mechanism  theory  is  one of the central modern
 theory of aging;  oxidizing-reduction homoeostasis,is believed,  to be
 central   in  stability  of  organism  from  intoxication  and  radial
 affection.  All types of modern anti-oxidants remedies, unfortunately,
 are  very toxic and its life-prolongation effects could not be used in
 humans for a long time.
    We investigated the EAS methods for preparation principally harmful
 agents from the water or weak solvent that may be used even in  1-2  L
 per day.


                 NEW COMPLEX SCIENTIFIC-RESEARCH PROGRAMME
 NEW BIOLOGICAL and PHYSICAL METHODS IN DIAGNOSTICS and TREATMENT of TUMOURS

    Researches workes  of Central research laboratory of Moscow medical
 stomatologocal institute of Ministry of Public Health,  Institute  for
 Physics  and  Institute  for  Chemical  Physics  of Russian Academy of
 Sciences,  Institute for Immunology of Academy of Medical Sciences  of
 Russia, Medical Institute of Vinniza took part in work.
   As a result of their work was shown:  - in the fields of fundamental
 researches  the  principally  new  mechanism  of immune control of the
 process of cell growth of non-immune types of tissues  was discovered;
 the  ability  of  definite types of T-lymphocytes to controll directly
 cell growth in the course  of  regeneration  induced  growth  of  many
 tissues  and  tumour  growth  was proved;the possibility to control of
 ---------------------------------------------------------------------------
                             - 25 -
 growth of transplanted tumours was achieved;
    - the  number  of  qualities  of  such  lymphocytes  and methods of
 influencing them  by  the  biologically  active  agents  and  physical
 factors  was  studied;  the  patent  on the method of defining factors
 secreted by such cells was  received  (  "Immunobiology  of  postnatal
 development":Moscow,   Science   (   Rus.);   Experimental   oncology,
 1989,N.5);
    - the  theory  of  "factors of low intensivity" was formulated.  It
 lets use  princilially  unharmful  and  highly  effective  methods  of
 effecting  by weak physical fields,  galvanic currents and small doses
 of biologicaly active,  natural ( in the first place ) means  for  the
 arms  of  diagnostics,  treatment  and  prophylaxis  ( "Factors of low
 intensivity in bioactivation and  immunocorrection",Moscow,1995(Rus.);
 Achievments of modern biology",1994, vol.114, p.160 ( Rus.); etc.
    - the  methods of bioimmunoactivation of apparatus and biologically
 active agents were worked out ( "Basis of  bioenergotherapy ",Vinniza,
 1991; Achievements of modern biology,1994, vol.114, p160 );
    - the possibilites of use of some physical factors  for diagnostics
 of  tumour  process  were researched - fluorescence of blood proteins,
 apearing along with tumour process,  and the changes in the  structure
 of biomagnetic field and biopotentials of body  surface of organism as
 well.
          THE CONTENTS OF WORKS.
    1. The  working out of experimantal approaches to growth regulatiom
 and differentiation of tumours on the basis of influencing  the immune
 systems of organism:  the newly discovered types of lymphocytes.  Must
 be studied;
    - enphasized  and characterized in detail types of such lymphocutes
 and factors secreted by them;
    - the  sensitiveness of such cells to various regulatory effectc of
 immunocorretive means in the first place and physical factors;
    - schemes  for  effecting  lymphocytes  of  such type for effecting
 lymphocytes of such type for control of tumour growth have been worked
 out;
 ---------------------------------------------------------------------------
                             - 26 -
    2. The working out of methods of growth control of tumour  cells by
 biologically active natural factors.  Must be studied:
    - possibilities of control of tumour cells growth and possibilities
 of induction of their differentiation by means of isolated from animal
 blod serum growth-correcting lypophylic proteins ( im cooperation with
 Centre of Maternity and Childhood ) and also the possibility of use of
 such proteins in a man with prophylactic and  treatment  aim,  and  as
 radioprotectors  and  anti-viral  means,  processing immuno-corrective
 activity;
    - the  possibility  to  correct  a  tumour  growth processes by new
 medicines, made on bases of natural components;  - the possibility  of
 correction of  tumour  process  with  application  of  weak  modulated
 magnetic field, for which the possibility of influencing the processes
 of tumour growth and differentiation is shown by our invastigations;
     3. The working out  of  new  methods  of  diagnostics  of  tumours
 processes  and  wide  use  for  screening  among  the  "risc" group of
 patients.  Must  be:  -  methods   of   fluorscence   diagnostics   of
 tumour-diagnostic blood proteins aproved;
    - methods  of  registration  of  biomagnetic  field   changes   and
 biopotentials  with  the  aim of diagnostics;
    - in the cooperation with the Institute  of  Traditional  treatment
 methods (  Ministru  of  Health of Russin Federation ) and taking into
 consideration out the  experiments  im  this  field  to  evaluate  the
 possibilities  of  use  of  method  of  bioenergoinformational  tumour
 diagnostics on the base of phenomenon of "supersensitiveness"  of some
 people to fields of low intensity.
   -------------------------------------------------------------------
               This publication is prepared with assistence
                    of FOUNDATION for LIFE PROLONGATION

                    WE ARE NEED OF SCIENCE CONTACTS AND
                 OF INTERNATIONAL FOUNDATIONS  ASSISTENCE

               E.MAIL:  agerus95@glas.apc.org  ( in GlasNet )

From owner-ageing@net.bio.net Fri Jul 07 23:00:00 1995
Path: biosci!agate!overload.lbl.gov!emf.emf.net!gatech!rutgers!oitnews.harvard.edu!purdue!mozo.cc.purdue.edu!not-for-mail
From: barani@mace.cc.purdue.edu (Barani)
Newsgroups: bionet.molbio.ageing
Subject: ageing or aging?! (on the lighter side)
Date: 8 Jul 1995 13:11:33 -0500
Organization: Purdue University
Lines: 9
Message-ID: <3tmhol$1cq@mace.cc.purdue.edu>
NNTP-Posting-Host: mace.cc.purdue.edu


   'Aging' might be better than 'ageing' but surely

   'dyeing' is better than 'dying'!

   :-)




From owner-ageing@net.bio.net Sun Jul 09 23:00:00 1995
Path: biosci!rutgers!gatech!news.uoregon.edu!vixen.cso.uiuc.edu!uchinews!news.luc.edu!jerikse
From: jerikse@news.luc.edu (Jason L. Eriksen)
Newsgroups: bionet.molbio.ageing
Subject: Re: Free Radicals in Cell Nuclei?
Date: 10 Jul 1995 20:56:37 GMT
Organization: Loyola University Chicago
Lines: 22
Message-ID: <3ts465$oij@apollo.it.luc.edu>
References: <3tli5v$utc@www.uno.edu>
NNTP-Posting-Host: bsd.meddean.luc.edu
X-Newsreader: TIN [version 1.2 PL2]

kgpl@uno.edu wrote:
: Someone has suggested to me that a lot of age-related damage may
: be the result of accidental miscopying of DNA due to the presence
: of free-radicals in cell nuclei messing up the copying process.
: Is this possible?  What kinds of free-radicals are generated within,
: or can get into, the nucleus of a cell?  Is there any reason to
: suspect that this sort of damage is more likely to occur during
: the process of cell division?

Oxygen-derived radicals, such as radicals and peroxides, seem to be byproducts
of a lot of cellular processes.  Cellular respiration, especially, seems to
generate huge amounts of free radicals in cells, most of which are mopped up
by superoxide dismutase and related free radical compensatory pathways.

Free radicals may cause cross-linkages of cell proteins to occur, leading to 
lots of junk to accumulate in the cell.  There is also a possibility that some
sort of DNA damage can occur via normal respiratory processes, although given
the efficiency of repair, permanent damage appears to be an infrequent  
occurance (thank goodness!).

Regards,
Jason Eriksen

From owner-ageing@net.bio.net Sun Jul 09 23:00:00 1995
Path: biosci!agate!howland.reston.ans.net!news.sprintlink.net!sjuvm!yprlbio
Nntp-Posting-Host: 149.68.2.20
Date: Mon, 10 Jul 1995 07:55:47 -0400
From: "LOCKSHIN, RICHARD A" <YPRLBIO@sjumusic.stjohns.edu>
Newsgroups: bionet.molbio.ageing
Subject: RE: cell-death meeting
Message-ID: <10JUL95.08563359.0022@sjumusic.stjohns.edu>
References: <v01510100ac21ce5c91b2@[142.20.6.185]>
Sender: usenet@sjumusic.stjohns.edu
Organization: St. John's University
Lines: 31

you just missed a gordon conference on cell death.  There are
a few commercially-sponsored meetings that crop up now and then,
especially in the west, such as the one currently advertized that
will be in Pittsburgh (look at cellbiol if it isn't here).  I doubt
that they will be as informative.  Watch in the areas of immunology,
including AIDS groups, cancer, and neurology.  Also, since you have
a Canadian address, there is a large group at the NRC Ottawa that
may sponsor a meeting.
Richard A. Lockshin/Dept. Biol. Sci. St. John's U. 8000 Utopia Pkwy
Jamaica NY 11439 USA/Phone 718: 990-1854/ Fax 718: 380-8543
In article <v01510100ac21ce5c91b2@[142.20.6.185]> shah@RESUNIX.RI.SICKKIDS.ON.CA writes:
>Hi,
>I am a PhD graduate student in yeast genetics and very close to graduation.
>I have decided that I would like to pursue the field of programmed cell
>death for my Post Doc and hopefully future career.  I would love to be able
>to go to a cell-death meeting this year to familiarize myself with the
>field and get to know the people in the field.  I know that there is a Cold
>Spring Harbour meeting coming in September, but I am told that it would be
>difficult to attend the meeting since I don't belong to a cell-death lab.
>Do you have any advice for me as to how I can attend this meeting, whether
>there are any other meeting that I might go to that is not as restricted
>and equally informative.  I thank you in advance for your help and
>suggestions.
>
>Sherry
>shah@resunix.ri.sickkids.on.ca
>
>
>.
>.


From owner-ageing@net.bio.net Sun Jul 09 23:00:00 1995
Path: biosci!agate!howland.reston.ans.net!news.sprintlink.net!noc.netcom.net!netcomsv!uu3news.netcom.com!netcomsv!uucp3.netcom.com!foodcom!FoodCom
From: FoodCom@foodcom.com (FoodCom)
Reply-To: FoodCom@foodcom.com
Newsgroups: bionet.molbio.ageing
Distribution: world
Subject: FoodCom News [Annoucement]
Date: 10 Jul 1995 06:35:04 GMT
Message-ID: <2633433086.84048463@foodcom.com>
Organization: FoodCom
Lines: 82


INTRODUCING "FOODCOM NEWS*"

Announcing the first and only "interactive" electronic on-line newspaper for
professionals in the food and beverage industry - "FoodCom News."
 
Now any professional working in or servicing the food and beverage industry
world-wide may contribute news, information and articles to this on-line
newspaper -- at no cost -- simply by sending email via the Internet to
foodcomnews@foodcom.com.  Members of the FoodCom* On-line Service may also
submit articles via FoodCom email.

This unique new service permits the world-wide members of the FoodCom On-line
Service to read an article and then reply directly to the author of the
article via email -- no matter where in the Internet world the article
originated.  This makes it easy for the reader to request more information,
and convenient for the author of the article to develop new business
relationships world-wide via electronic mail.  FoodCom members can even use
FoodCom's powerful search capabilities to "read" FoodCom News and create
their own custom newspaper by automatically gathering those articles of
specific interest.

SUGGESTIONS FOR USING "FOODCOM NEWS"

Use "FoodCom News" to publish news and information about yourself, your
company or anything you believe is newsworthy to the food and beverage
industry.  

Here are some ideas for how to use "FoodCom News."
* Announce your membership at FoodCom and tell how you would like to use
FoodCom to communicate and do business with the industry.
* Build awareness of your Internet email addresses or World Wide Web site
among professionals in the food and beverage industry. 
* Publish an article about food and beverage trends.
* Make the food industry aware of an upcoming convention, seminar or event.
* Introduce new products and services.
* Report organizational changes.
* Publish an article about your services and products.
* Post messages about employment opportunities or seek career advancement.

The possibilities are endless to how you can use this opportunity to keep
FoodCom members well informed.

TO SUBMIT AN ARTICLE VIA INTERNET EMAIL

If you, or someone you know, would like to submit an article to "FoodCom
News" via the Internet, simply send your article as an email message and
address it to: foodcomnews@foodcom.com

Hints & tips:
1) Write a short, yet clear topic description in the subject line of your
email heading.  Try to stay within 25 characters.
2) Check for spelling.
3) Ask for readers to reply via email or take some kind of action.
4) Be sure to include in your article any information about how to contact
you or your company.

Articles submitted to "FoodCom News" are first read by FoodCom System
Operators and then approved for public viewing.  This is done to screen-out
any irrelevant electronic "junk mail" -- a necessary step as "FoodCom News"
is open to any user of the Internet.  Announcements and articles sent and
approved will be published as submitted.  In one to two business days you
will receive an email confirmation from FoodCom that your article has been
published in "FoodCom News."

We look forward to your contributions to "FoodCom News" and hope you find it
a valuable means of keeping the food and beverage industry informed.  

If you have any questions or comments, or would like more information about
FoodCom, please contact us at:
Email:  info@foodcom.com
WWW:  http://www.foodcom.com/foodcom/
Ph:  (415) 637-8319
Fax: (415) 637-7751

See you on-line,
FoodCom

-----------------------------------------------------------
This message was sent via FoodCom.
info@foodcom.com   Ph:(415) 637-8319  http://www.foodcom.com/foodcom/


From owner-ageing@net.bio.net Sun Jul 09 23:00:00 1995
Path: biosci!IUNHAW1.IUN.INDIANA.EDU!TSTABLER
From: TSTABLER@IUNHAW1.IUN.INDIANA.EDU ("Tim Stabler")
Newsgroups: bionet.molbio.ageing
Subject: Questions
Date: 10 Jul 1995 07:57:19 -0700
Organization: Indiana University Northwest
Lines: 29
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <6323BA2FB7@iunhaw1.iun.indiana.edu>
NNTP-Posting-Host: net.bio.net

I have been on this net for a couple weeks and, now that I have read 
some mail, woyld like to post two questions for the group.

1.  Is there anyone else on the net that teaches a biology of aging 
course?  I am teaching a class I developed for Indiana University 
called "Biological Aspects of Aging" and I really enjoy it.  I was 
curious what others are using for texts (I use the book by DiGiovanna 
of Salibury State) and how you might cover various topics.  Any 
comments would be welcome.

2.  I was at a meeting about animal care and a fellow from Washington 
that works with a NIH search group or something (I lost references) 
said that Medline only covers about half of what is published.  I do 
go out to decubitus ulcer meetings (although not that much recently 
due to the sponsoring company wanting to go in other directions) and 
talk on the aging of the skin and immune system.  I also add in info 
on ulcers and burns in the older person----all related to skin aging.
Wanting to keep my material up-to-date, my question is what is the 
"other half" and how do I access it?

Thanks for the info.

DR. Tim Stabler
Department of Biology
Indiana University Northwest
Gary, Indiana 46408

219-980-6718
FAX:219-980-7125

From owner-ageing@net.bio.net Sun Jul 09 23:00:00 1995
Path: biosci!agate!howland.reston.ans.net!news.sprintlink.net!sjuvm!yprlbio
Nntp-Posting-Host: 149.68.2.20
Date: Mon, 10 Jul 1995 07:58:05 -0400
From: "LOCKSHIN, RICHARD A" <YPRLBIO@sjumusic.stjohns.edu>
Newsgroups: bionet.molbio.ageing
Subject: RE: cell-death meeting
Message-ID: <10JUL95.08604941.0022@sjumusic.stjohns.edu>
References: <v01510100ac21ce5c91b2@[142.20.6.185]>
Sender: usenet@sjumusic.stjohns.edu
Organization: St. John's University
Lines: 27

Follow-up:  If "sick-kids means Hospital for Sick Children,
Toronto, watch also if U of Rochester has any symposia or, if
you get to New York, we have an active cell death club that meets
once per month.
Richard A. Lockshin/Dept. Biol. Sci. St. John's U. 8000 Utopia Pkwy
Jamaica NY 11439 USA/Phone 718: 990-1854/ Fax 718: 380-8543
In article <v01510100ac21ce5c91b2@[142.20.6.185]> shah@RESUNIX.RI.SICKKIDS.ON.CA writes:
>Hi,
>I am a PhD graduate student in yeast genetics and very close to graduation.
>I have decided that I would like to pursue the field of programmed cell
>death for my Post Doc and hopefully future career.  I would love to be able
>to go to a cell-death meeting this year to familiarize myself with the
>field and get to know the people in the field.  I know that there is a Cold
>Spring Harbour meeting coming in September, but I am told that it would be
>difficult to attend the meeting since I don't belong to a cell-death lab.
>Do you have any advice for me as to how I can attend this meeting, whether
>there are any other meeting that I might go to that is not as restricted
>and equally informative.  I thank you in advance for your help and
>suggestions.
>
>Sherry
>shah@resunix.ri.sickkids.on.ca
>
>
>.
>.


From owner-ageing@net.bio.net Mon Jul 10 23:00:00 1995
Path: biosci!POSSUM.MURDOCH.EDU.AU!cummins
From: cummins@POSSUM.MURDOCH.EDU.AU (Dr Jim Cummins)
Newsgroups: bionet.molbio.ageing
Subject: Re: Free Radicals in Cell Nuclei?
Date: 10 Jul 1995 18:10:35 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 38
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <v01510106ac277d2896fc@[134.115.81.42]>
NNTP-Posting-Host: net.bio.net

>kgpl@uno.edu wrote:
>: Someone has suggested to me that a lot of age-related damage may
>: be the result of accidental miscopying of DNA due to the presence
>: of free-radicals in cell nuclei messing up the copying process.
>: Is this possible?

jerikse@apollo.it.luc.edu  wrote

>Oxygen-derived radicals, such as radicals and peroxides, seem to be byproducts
>of a lot of cellular processes.  Cellular respiration, especially, seems to
>generate huge amounts of free radicals in cells, most of which are mopped up
>by superoxide dismutase and related free radical compensatory pathways.

Most if not all oxidative metabolism (the major generator of free radicals)
is confined to mitochondria.  Some think that sequestering this dangerous
business away from the nucleus to these sacrificial "slave" organelles is
essential to minimise the danger to the somatic genome.

Lindahl, T. (1993). Instability and decay of the primary structure of DNA.
Nature, Lond, 362, 709-725.

Max, B. (1992). This and that: hair pigments, the hypoxic basis of life and
the Virgilian journey of the spermatozoon. Trends Pharmacol Sci, 13,
272-276.


Jim "Spermatology rules o~ o~ o~ o~" Cummins

Associate Professor in Veterinary Anatomy
Murdoch University, Western Australia 6150
Tel +61-9-360 2668, Fax +61-9-310 4144
E mail <cummins@possum.murdoch.edu.au>
URL <http://Numbat.murdoch.edu.au/spermatology/spermhp.html>
"An inordinate fondness for Beetles" (Haldane on God).





From owner-ageing@net.bio.net Mon Jul 10 23:00:00 1995
Path: biosci!ilr.rc.ac.ru!gavrilov
From: gavrilov@ilr.rc.ac.ru ("Leonid A.Gavrilov")
Newsgroups: bionet.molbio.ageing
Subject: Lectures on Gerontology and Longevity Research
Date: 11 Jul 1995 09:51:46 -0700
Organization: A.N.Belozersky Institute
Lines: 184
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <ADLth0mC5N@ilr.rc.ac.ru>
NNTP-Posting-Host: net.bio.net


Dear Colleagues,

   On August-September, 1995  Dr.Natalia S.Gavrilova, Ph.D. and myself
will be travelling across the Europe (The Netherlands, Belgium, France,
Great Britain, etc.) giving lectures and seminars based on our research
work.

   The purpose of these seminars is to establish scientific collaboration
and to collect funds for establishing the Institute for Longevity Research
in Moscow (the first gerontological institute in the history of Russia !).

   Now we are forming the schedule of our visits and seminars and we would
be happy to consider any invitations and suggestions in this direction.

   We already had very positive experience with our lectures in Germany,
France, United Kingdom and USA. Our lectures are based on the recent
progress in our research work and our book:

          THE BIOLOGY OF LIFE SPAN: A QUANTITATIVE APPROACH

that received a lot of positive reviews in the leading scientific
journals by the leading gerontologists (see attachment printed below).

   Sincerely yours,

   Dr.Leonid A.Gavrilov, Ph.D.
   Member of the Council of Russian Gerontological Society

P.S.: Recommendations of our lectures based on our book are printed below.
***************************************************************************

"HIGHLY RECOMMENDED FOR STIMULATING FRESH APPROACHES ... " -
Professor Roy L.Walford, M.D., UCLA School of Medicine, USA.
   THE GERONTOLOGIST, 1991, vol.31, No.5, p.707.

"CLEARLY,  THIS   IS   A   VERY   INTERESTING,   PROVOCATIVE   AND
THOUGHT-PROVOKING BOOK" - Dr. Ward  Dean,  M.D.,  The  Center  for
Bio-Gerontology,  Pencasola,  Florida,  USA.
   EXPERIMENTAL GERONTOLOGY, 1992, vol.27, No.2, pp.251-253.

"THIS IS  AN  INTERESTING  BOOK,  FULL  OF  TABLES  AND  DATA  AND
POLEMICAL IN ITS APPROACH." - Professor William A.Pryor,  Director
of Biodynamic Institute, Louisiana State University, Baton  Rouge,
LA,USA.
   FREE RADICAL BIOLOGY & MEDICINE, 1992, vol.12, pp.331-332.

"IT BRINGS TO BEAR A FRESH  APPROACH  WHOSE  IDEAS  ARE  LOGICALLY
PRESENTED AND DEVELOPED". - Dr. Brian Merry, Ph.D., Institute  of
Human  Aging, University of Liverpool, United Kingdom.
   AGEING AND SOCIETY, 1991, vol.11, No.4, pp.509-510.

"GOOD NEW BOOK ON AGEING". - Dr. Thomas B.L.Kirkwood, Ph.D.
Head of the Laboratory of Mathematical Biology, National
Institute for Medical Research, London, United Kingdom.
   NATURE, 1991, vol.352, 29 August, pp.767-768.

"... SHOULD BE READ BY ANYONE SERIOUSLY INTERESTED IN AGEING.  ...
YOU WILL FIND THIS A SURPRISINGLY GOOD  'READ',  AND  A  MUST  FOR
EVERY  LIBRARY".  -  Dr.   D.Sebastian   Fairweather,   Physician,
   Department of Geriatric Medicine, Oxford, United Kingdom.
   AGE AND AGEING, 1992, vol.21, No.5, pp.386-387.

"THE BOOK FEATURES QUITE A BIT OF DEMOGRAPHIC THEORY AND ANALYSIS.
... IT IS REFRESHING"  -  Professor Michael R.Rose, University  of
   California, Irvine, USA.
   ANNALS OF HUMAN BIOLOGY, 1992, vol.19, No.3, pp.320-321.

"THE GAVRILOVS HAVE MADE A VALUABLE CONTRIBUTION TO THE  STUDY  OF
LIFE SPAN, AND ANY FUTURE WORK ON THE SUBJECT WILL  HAVE  TO  TAKE
ACCOUNT OF THE RICH CONTENTS OF THIS BOOK". - Dr. Vaino Kannisto,
Former United Nations Adviser on Demography
   POPULATION STUDIES, 1992, vol.46, No.2, pp. 366-367.

"EIN AKTUELLES BUCH, DAS SICHERLICH DIE INTERNATIONALE
DISKUSSION DES PROBLEMS BEFORDERN KANN."
 - Prof. Dr. Ingeborg Falck, Berlin, Germany.
   ZEITSCHRIFT FUR GERONTOLOGIE, 1991, Band 25, Heft 1, S.56.

"THE BOOK IS WELL WRITTEN, EASY TO READ, AND SHOULD BE OF INTEREST
TO A WIDE SPECTRUM OF READERS  INCLUDING  PHYSICIANS,  BIOLOGISTS,
BIOCHEMISTS, GERONTOLOGISTS..."
 - Prof. Robert W.Gracy, University of North Texas, USA.
   EDUCATIONAL GERONTOLOGY, 1993, vol.19, No.1, pp.92-93.

"...  THIS  BOOK  IS  A  HIGHLY  VALUABLE  CONTRIBUTION   TO   THE
DISCIPLINE. ...THIS BOOK SHOULD MAKE  SCIENTISTS  TAKE  NOTICE  OF
RESEARCH ON AGING AND LONGEVITY ... IN THE FORMER SOVIET UNION" -
    Dr.  S.Jay Olshansky, Ph.D., University of Chicago, USA
POPULATION AND DEVELOPMENT REVIEW, 1992, vol.18, No.3, pp.555-558.

"... MANY WILL FIND AN EXCURSION INTO IT STIMULATING".
 - Dr. Emily Grundy, Lecturer in Gerontology, Age Concern
   Institute of Gerontology, King's College, London, UK.
   BRITISH MEDICAL JOURNAL, 1992, vol.305, No.6850, p.431.

"GAVRILOV MAKES THE BEST ATTEMPT I KNOW OF TO DISTINGUISH HOW LONG
PEOPLE COULD LIVE FROM HOW LONG THEY ACTUALLY LIVE -  ONE  OF  THE
MORE DIFFICULT TASKS FOR BOTH BIOLOGY AND STATISTICS... GAVRILOV'S
SCHOLARSHIP  IS   IMPRESSIVE".   -   Professor   Nathan   Keyfitz,
   International   Institute   for   Applied   Systems   Analysis,
   Laxenburg, Austria.
   MATHEMATICAL POPULATION STUDIES, 1991, vol.3, No.2, p.161.

"LEONID  GAVRILOV   IS   A   TOP-FLIGHT   STATISTICAL   POPULATION
BIOLOGIST... THE AREA IS IMPORTANT WELL  BEYOND  THE  CONFINES  OF
BIOLOGICAL  GERONTOLOGY  AND  EXTENDS  INTO  POLITICS  AND  SOCIAL
PLANNING. GAVRILOV IS VERY GOOD ON JUST THIS SORT OF THING. HE HAS
A FRESH APPROACH, NEW IDEAS, A GREAT  DEAL  OF  DATA  NOT  READILY
AVAILABLE ELSEWHERE." - Roy. L. Walford, Professor  of  Pathology,
   UCLA School of Medicine, USA.
   MATHEMATICAL POPULATION STUDIES, 1991, vol.3, No.2, p.161.

"THIS  BOOK  IS  DIRECTED   TOWARD   RESEARCHERS   INTERESTED   IN
STATISTICAL PATTERNS AND MATHEMATICAL MODELS OF HUMAN  LIFE  SPAN.
FOR STUDENTS WITHIN THIS  DEFINED  AREA  OF  RESEARCH,  THIS  TEXT
OFFERS A GOOD HISTORICAL PERSPECTIVE,  INSIGHT  INTO  THE  RUSSIAN
LITERATURE, AND INSIGHT INTO THE  QUANTITATIVE  ANALYSIS  OF  LIFE
SPAN"   -   Dr.  Deborah  A.Roach,  Department  of  Zoology,
    Duke University, Durham, USA.
    ECOLOGY, 1992, vol.73, No.1, pp.379-381.

"THIS BOOK IS IN ESSENCE A BIOSTATISTICAL ANALYSIS OF THE PROBLEMS
OF  LIFESPAN,  HUMAN  AND  ANIMAL.  ...  THE  LITERATURE  IN  MANY
LANGUAGES HAD CLEARLY BEEN WELL COVERED, AND MUCH HAS BEEN MADE OF
NATIONAL AND OTHER MORTALITY STATISTICS IN  THIS  CENTURY.  ...
A USEFUL SOURCE BOOK." - Dr. F.I.Caird, D.M., F.R.C.P.,  Professor
   of Geriatric Medicine, Southern General Hospital, Glasgow, UK.
   J. OF CLINICAL AND EXPERIMENTAL GERONTOLOGY, 1992, vol.14,
   No. 3 & 4, p.309.

"THIS INTELLIGENT AND THOUGHT PROVOKING BOOK SHOULD BE READ WIDELY"
  -  Dr. Suresh I.S.Rattan,  Ph.D., Laboratory of Cellular Ageing,
   Aarhus University, Denmark.
   INDIAN JOURNAL OF EXPERIMENTAL BIOLOGY, 1993, vol.31, p.499-500.

"... THE READER WILL BENEFIT ENORMOUSLY  FROM  THE  BROADENING  OF
PERSPECTIVE AS A RESULT OF EXPOSURE TO THE GAVRILOVS' THEORIES  ON
THE BIOLOGY OF LIFE SPAN"    -   Dr. M. Michael  Akiyama,
   University of Michigan, Dearborn, USA.
   HUMAN BIOLOGY, 1992, vol.64, No.4, pp.630-632.

"THIS IS A PROVOCATIVE AND REFRESHING BOOK" - Dr.Alan R.Hipkiss,
   Age Concern Institute of Gerontology, King's College London, UK.
 INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY, 1992, vol.7,No.8,p.614.

"THIS BOOK SHOULD  BE  READ  BY  ALL  MEMBERS  OF  THE  PROFESSION
INTERESTED IN MORTALITY - WHICH  SHOULD  BE  ALL  MEMBERS  OF  THE
PROFESSION" -  Dr. H.A.R.Barnett, Institute of Actuaries, UK.
 J.OF THE INSTITUTE OF ACTUARIES, 1992, vol.119, Part II, pp.379-381.

"TO SUM UP, THE BOOK IS SUBSTANTIAL, INTERESTING AND BRINGS  FRESH
AIR. WE CAN CONFIDENTLY COMMEND ITS STUDY TO ALL SCIENTISTS ... "
   - Dr. Janos Izsak, Department of Zoology, Berzsenyi Teachers'
   College, Szombathely, Hungary.
ARCHIVES OF GERONTOLOGY AND GERIATRICS, 1992, vol.15, No.2,pp.192-194.

"A GENERAL THEORY OF LIFESPAN IS THUS CREATED." -
 - Dr. Norman Vetter, University Hospital of Wales, Cardiff, UK.
J.OF EPIDEMIOLOGY & COMMUNITY HEALTH, 1992, vol.46, No.6, p.630.

"I FOUND IT TO BE HIGHLY REWARDING READING." -
   Dr. Edward J.Masoro, University of Texas Health Science Center.
   QUARTERLY REVIEW OF BIOLOGY, 1993, vol.68, p.92.

"THIS ... IS AN EXCELLENT BOOK. ... NOBODY INTERESTED IN AGING SHOULD
FAIL TO READ". -
   Dr. C.S.Downes, Department of Zoology, University of Cambridge, UK.
   BIOESSAYS, 1993, vol.15, No.5, pp.359-362.

"...PROVOCATIVE AND ENTERTAINING READING AND CAN BE RECOMMENDED TO
ANYONE WITH AN INTEREST IN BIOLOGICAL AGING." -
   Dr. Douglas E.Crews, Department of Anthropology, Ohio State
   University, USA
   JOURNAL OF CROSS-CULTURAL GERONTOLOGY, 1993, vol.8, No.3, pp.281-290.

"IT DESERVES TO BE READ WIDELY. SCIENTISTS AND PHYSICIANS WHO ARE
INTERESTED IN THE AGING OF POPULATIONS OR OF INDIVIDUALS WILL BE MUCH
MORE EFFECTIVE IN THEIR WORK IF THEY BECOME FAMILIAR WITH THE SUBJECT
MATTER OF THIS BOOK." -
    JOURNAL OF ORTHOMOLECULAR MEDICINE, 1993, vol.8, No.1, pp.59-60.
**********************************THE END********************************



From owner-ageing@net.bio.net Tue Jul 11 23:00:00 1995
Path: biosci!ihnp4.ucsd.edu!news.service.uci.edu!usenet
From: KUCI Fan <Me@uci.edu>
Newsgroups: bionet.molbio.ageing
Subject: Re: REGISTRATION IS IN PROGRESS FOR APOPTOSIS SYMPOSIUM
Date: 12 Jul 1995 20:49:55 GMT
Organization: Unemployed, Inc.
Lines: 36
Message-ID: <3u1chj$2lb@news.service.uci.edu>
References: <Pine.3.89.9507070707.A22681-0100000@SINGER.ASRI.EDU>
NNTP-Posting-Host: curly.bio.uci.edu
Mime-Version: 1.0
Content-Type: multipart/mixed;
	boundary="-------------------------------18977111614357"
X-Mailer: Mozilla 1.1N (Macintosh; I; PPC)
To: MANEV@SINGER.ASRI.EDU
X-URL: news:Pine.3.89.9507070707.A22681-0100000@SINGER.ASRI.EDU

This is a multi-part message in MIME format.

---------------------------------18977111614357
Content-Transfer-Encoding: 7bit
Content-Type: text/plain; charset=us-ascii

MANEV@SINGER.ASRI.EDU wrote:
>International Symposium on Oxidative Stress, Apoptosis and Brain Damage
>will be held in Pittsburgh, PA from September 21 to 24.
>Registration is in progress ($ 250, three days; includes course materials,
>welcome reception, continental breakfast, lunch and refreshment breaks 
>each day).
>For information please call: +412-359-4952.
>


---------------------------------18977111614357
Content-Transfer-Encoding: 7bit
Content-Type: text/plain

From: MANEV@SINGER.ASRI.EDU
Newsgroups: bionet.molbio.ageing
Subject: REGISTRATION IS IN PROGRESS FOR APOPTOSIS SYMPOSIUM
Date: 7 Jul 1995 04:52:12 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Message-ID: <Pine.3.89.9507070707.A22681-0100000@SINGER.ASRI.EDU>

International Symposium on Oxidative Stress, Apoptosis and Brain Damage
will be held in Pittsburgh, PA from September 21 to 24.
Registration is in progress ($ 250, three days; includes course materials,
welcome reception, continental breakfast, lunch and refreshment breaks 
each day).
For information please call: +412-359-4952.


---------------------------------18977111614357--

From owner-ageing@net.bio.net Fri Jul 14 23:00:00 1995
Path: biosci!VMSA.CSD.MU.EDU!6534HEINTZT
From: 6534HEINTZT@VMSA.CSD.MU.EDU
Newsgroups: bionet.molbio.ageing
Subject: Aging resources needed
Date: 14 Jul 1995 21:27:55 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 22
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <01HSVMD3EEYE91YJUR@VMS.CSD.MU.EDU>
NNTP-Posting-Host: net.bio.net

Hello, I need your help.
  
I am writing a book which contains a list of useful resources for senior 
citizens in all lifestyles.  If your organization/company offers a 
service/product which you believe would be useful to seniors, please 
E-Mail (6534HEINTZT@VMS.CSD.MU.EDU) the following:

    Company name
    Full address
    Phone numbers

    Brief (20 words max.) description of product/service.

    There is NO CHARGE for being listed.

Thank you.

Rita J. Putnam, author
AS YOUR PARENTS AGE - 1994
AS WE AGE - 1995
GOLDEN-AGERS RESOURCE DIRECTORY - 1995
http://www.alpha.net/dci/aging.html

From owner-ageing@net.bio.net Fri Jul 14 23:00:00 1995
Path: biosci!daresbury!trane.uninett.no!Norway.EU.net!EU.net!news.sprintlink.net!tank.news.pipex.net!pipex!demon!longevb.demon.co.uk!John
From: John de Rivaz <John@longevb.demon.co.uk>
Newsgroups: bionet.molbio.ageing
Subject: Re: Aging resources needed
Date: Sat, 15 Jul 1995 10:46:36 GMT
Organization: Myorganisation
Lines: 13
Message-ID: <470925683wnr@longevb.demon.co.uk>
References: <01HSVMD3EEYE91YJUR@VMS.CSD.MU.EDU>
Reply-To: John@longevb.demon.co.uk
X-NNTP-Posting-Host: longevb.demon.co.uk
X-Broken-Date: Saturday, Jul 15, 1995 10.46.36
X-Newsreader: Newswin Alpha 0.7

There was a book published in 1980 called The Complete Book of 
Longevity by Rita *Aero* and published by *Putnam*. Is there any 
connection?

-- 
Sincerely,     ****************************************       
               * Publisher of        Longevity Report *
John de Rivaz  *                     Fractal Report   *
               *          details on request          *
               ****************************************
**** What is the point of life if it ends in death? ****


From owner-ageing@net.bio.net Mon Jul 17 23:00:00 1995
Newsgroups: bionet.molbio.ageing
Path: biosci!galaxy.ucr.edu!ratatosk.yggdrasil.com!news.duke.edu!convex!cs.utexas.edu!swrinde!dish.news.pipex.net!pipex!warwick!bsmail!usenet
From: Harry Witchel
Subject: Pineal gland, ageing, research in US, UK, GDR, Japan
Message-ID: <DBwx64.Hor@uns.bris.ac.uk>
Sender: usenet@uns.bris.ac.uk (Usenet news owner)
Nntp-Posting-Host: rm2.pys.bris.ac.uk
Reply-To: harry.witchel@bristol.ac.uk
Organization: Medical School, Bristol, UK
X-Newsreader: WinVN 0.91.4
Date: Tue, 18 Jul 1995 12:54:03 GMT
Lines: 23

	It seems that in the US, UK, Germany, and Japan the thrust of 
funding in ageing in mammals is in extrinsic causes (eg RG_Cutler 
(1978) "Evolutionary Biology of Senescence" in _Biology of Aging_ 
edited by JA Behnke (New York, Plenum) pp. 311-60; and D_Harman (1992) 
"Free Radical Theory of Aging" _Mutation Research_ 275:257-66) and 
dietary restriction (eg EJ_Masoro (1992) "A Dietary Key to Uncovering 
Aging Processes" _News in Physiological Sciences_ 7:157-160).
	When literature searching I have found conference proceedings 
from small groups in Russia and Italy suggesting that pineal 
transplant (or even night-time feeding of melatonin) can lead to 
increased mean lifespans in rats (eg VA Lesnikov & W Pierpaoli (1994) 
"Pineal cross transplantation (Old-to-Yound and vice versa) as 
evidence for an Endogenous Aging Clock" Annals NY Acad. Sciences 
719:456-460).  With the exception of W Regelson (Piepaoli's 
collaborator from Richmond, VA) there seems to be no follow up on this 
important work, especially curious as there is not (to my knowledge) 
any demonstration in mammals that  adding oxygen radical scavengers 
increases lifespans.
	I assume that the lack of follow-up in the US, UK, Germany, 
and Japan is due to the skepticism.  Has there been any US pursuit of 
this idea?  Is there evidence for radical scavengers increasing 
lifespan in mammals?
Harry Witchel

From owner-ageing@net.bio.net Tue Jul 18 23:00:00 1995
Path: biosci!daresbury!trane.uninett.no!Norway.EU.net!EU.net!howland.reston.ans.net!news.sprintlink.net!news.voicenet.com!cherryhill11.voicenet.com!mortgale
From: mortgale@omni.voicenet.com (Morten Gale)
Newsgroups: bionet.molbio.ageing
Subject: Melatonin Dosage
Date: Wed, 19 Jul 1995 21:00:27 GMT
Organization: Voicenet - Internet Access - (215)674-9290
Lines: 14
Message-ID: <mortgale.12.300D726A@omni.voicenet.com>
NNTP-Posting-Host: cherryhill11.voicenet.com
Summary: Is there a recommended dosage?
Keywords: melatonin, dosage
X-Newsreader: Trumpet for Windows [Version 1.0 Rev B final beta #4]

An article by Janet Raloff in Science News (Vol 147 No. 19, pg 300-301) 
described several benefits of taking melatonin as an aid for sleep, aging 
(antioxidant), breast cancer, etc.

Does anyone know where I can find more information about the appropriate 
dosage and timing for using melatonin as an aid for sleeping and anti-aging (I 
am 70)? I have some 3mg Melatonin tablets from KAL, who suggest 1 - 2 
tablets, 20 minutes before going to sleep. Is that the only time that they can 
be taken? Or can they be taken at other times for their anti-aging benefits? 
Is there a detrimental consequence of taking more than the recommended dose?

Any suggestions for further sources of information would be appreciated.

Mort Gale  

From owner-ageing@net.bio.net Wed Jul 19 23:00:00 1995
Path: biosci!daresbury!trane.uninett.no!Norway.EU.net!EU.net!howland.reston.ans.net!ix.netcom.com!netnews
From: pootszu@ix.netcom.com (Susan Patrick )
Newsgroups: bionet.molbio.ageing
Subject: DHEA's effects on aging
Date: 18 Jul 1995 02:36:17 GMT
Organization: Netcom
Lines: 45
Distribution: world
Message-ID: <3uf6n1$7o6@ixnews2.ix.netcom.com>
NNTP-Posting-Host: ix-cin4-08.ix.netcom.com

I was recently introduced to several very interesting articles about
DHEA, and would like to share them with you.

Excerpt From: The New England Journal of Medicine, no date

"Scientists are wondering whether they may have at last found the root
cause of aging itself.  Provoking intense excitement among longevity
researchers is a new report from California on a steroid called DHEA
(dehydroepiandrosterone) that appears to reduce the risk of heart
disease."
"In a study of 242 men over age 50, researcher Elizabeth Barrett-Connor
at the University of California at San Diego found that those with high
levels of DHEA in their blood were only half as likely to die of heart
disease as those with relatively little of the hormone. Even with
people without heart disease, DHEA seems to protect against early
death."
"On its own, that's good news. But coming as it does after reports that
taking DHEA can prevent or ease a variety of other ills, it may be the
strongest evidence yet that a single hormone plays a central role in
maintaining human health." 


Excerpt From: LIFE magazine, October, 1992

     Nature believes in overkill.  Determined to ensure our survival
until we can reproduce, nature has crammed the human organism with
backup systems.  One of the most effective is DHEA (short for
dehydroepiandrosterone), an adrenal hormone that, much like human
growth hormone, floods the body while we're young and has various
powerful beneficial effects on the human system.
     As we enter out thirties, production of DHEA begins to ebb.  At
50, most people secrete only 30 percent of what they produced when they
were young, and the loss can trigger catastrophes. A DHEA deficiency
can increase the risk of breast cancer in women and heart attacks in
men.
     But Dr. Arthur Schwarts, 51, a Temple University biologist and
leading U.S. autrhority on the hormone, reports that in laboratory
animals high dose DHEA feedings reduce body fat by one third, prevent
atherosclerosis, alleviate diabetes, reduce the risk of cancer, enhance
the immune response, inhibit the development of certain autoimmune
diseases and extend the bnormal life span of mice by 20 percent. 

For more information on DHEA, please e-mail me at
pootszu@ix.netcom.com


From owner-ageing@net.bio.net Wed Jul 19 23:00:00 1995
Path: biosci!rutgers!uwm.edu!vixen.cso.uiuc.edu!howland.reston.ans.net!torn!newshub.ccs.yorku.ca!shemp15.slip.yorku.ca!kathylee
From: kathylee@yorku.ca (Catherine Lee)
Newsgroups: bionet.molbio.ageing
Subject: Looking for Novel Therapeutic Proteins for Licensing
Date: Thu, 20 Jul 1995 12:32:23 GMT
Organization: York University
Lines: 15
Message-ID: <kathylee.8.300E4CD7@yorku.ca>
NNTP-Posting-Host: shemp15.slip.yorku.ca
X-Newsreader: Trumpet for Windows [Version 1.0 Rev B final beta #4]


I am requesting information on any novel therapeutic proteins that are 
available for licensing for development/ production in E. coli system.  The E. 
coli system has been used to produce bioactive human PTH and human EGF at 
levels for commercialization.   I am interested in finding new or existing 
peptides or proteins with known or implied therapeutic activity.  If you or 
your colleagues have available or know of such a protein (or proteins), I 
would be very interested in discussing its future development and/or 
manufacturing requirements. 

Please reply via e-mial: kathylee@yorku.ca

Thanks for your help in advance.

Catherine Lee, Ph.D.

From owner-ageing@net.bio.net Fri Jul 21 23:00:00 1995
Path: biosci!agate!howland.reston.ans.net!news.sprintlink.net!news.clark.net!rahul.net!a2i!kaiwan.kaiwan.com!not-for-mail
From: jlin@kaiwan009.kaiwan.com (Neptune)
Newsgroups: bionet.molbio.ageing
Subject: ACAM fall convention announcement
Date: 22 Jul 1995 10:28:33 -0700
Organization: KAIWAN Internet (310-527-4279,818-756-0180,909-785-9712,714-638-4133,805-294-9338)
Lines: 51
Message-ID: <3urcg1$o4@kaiwan009.kaiwan.com>
NNTP-Posting-Host: kaiwan009.kaiwan.com
X-Newsreader: TIN [version 1.2 PL2]


American College for Advancement in Medicine (ACAM) will hold its fall
convention at Colorado Springs, Colorado on November 2-5 1995.
Along with Chelation therapy workshop be held on Nov 1-2 1995.

The theme of this convention will be:

 AGING: REDUCING, REVERSING AND COPING WITH ITS EFFECTS. 

Following are some of the confirmed speakers and topics

Jeffery Bland, PhD
Physiological Oxidation/Reduction and its Relationship
to Biological Aging.

Jeffery Blumberg, PhD
Recent Advances in Nutrition and Aging Research: Antioxidants,
Calcium and other nutrients.

LeoGalland, MD
The aging gut

Richard A. Kunin MD
Copper balance and aging

Simin Meydani, DVM, PhD
Vit B6 and E, and Immune function in the elderly.

Richard Passwater, PhD
Synergistic Approaches to reducing oxidative and Glycosylation
damage reactions of the aging process.

....and much more.


Any questions or registration(discount apply to member and advance 
registrant, before Oct 2). Please contact

ACAM
23121 Verdugo Dr. Suite 204
Laguna Hills, CA 92653

Tel: 800-532-3688  or 714-583-7666
-- 
John Lin     *** Save the planet, save the world ! ***

e-mail: jlin@kaiwan.com
-- 
John Lin     *** Save the planet, save the world ! ***

e-mail: jlin@kaiwan.com

From owner-ageing@net.bio.net Mon Jul 24 23:00:00 1995
Path: biosci!bcm!news.msfc.nasa.gov!europa.chnt.gtegsc.com!gatech!news.sprintlink.net!news.voicenet.com!cherryhill22.voicenet.com!mortgale
From: mortgale@omni.voicenet.com (Morten Gale)
Newsgroups: bionet.molbio.ageing
Subject: Melatonin Dosage II
Date: Mon, 24 Jul 1995 19:07:26 GMT
Organization: Voicenet - Internet Access - (215)674-9290
Lines: 36
Message-ID: <mortgale.13.3013EF6E@omni.voicenet.com>
NNTP-Posting-Host: cherryhill22.voicenet.com
Summary: Responses to my first post on this Subject.
Keywords: melatonin, dosage
X-Newsreader: Trumpet for Windows [Version 1.0 Rev B final beta #4]

In an earlier post I asked for information on the appropriate dosage for using 
melatonin as an aid for sleep and  antiaging.

I received two email responses which I want to share with others who may have 
seen the first posting. (Because they were email responses, I won't identify 
them since I don't know if that is their desire.)

A 40 y/o said that she takes 3mg about a half hour before going to bed. This 
is consistent with what I found from a second source, who offered the 
following.

<There's a new book called "Staying Young The Melatonin Way" by Steven J. Bock 
and Michael Boyette (Dutton Signet). It's excerpted in "Longevity" magazine 
for August 1995.>

I found both the book ($18.95) and the magazine ($2.99) at a local Dalton's 
Book Store. Both were exceptionally informative with respect to current 
understandings of the effects of melatonin. The magazine article carries most 
of the information that's in the book. I feel much better informed after 
reading these sources. 

The second email response to my post also suggested other sources of Net 
advice on aging and related topics. These other sources were as follows:

Newsgroups:   sci.life-extension;  sci.med.nutrition; and sci.med.pharmacy 
WWW Sites:  http://pharminfo.com;   http:www.usc.edu/dept/nbio/nibs.html; and 
http://www.hookup.net/mall/aging/agesit59.html.

I want to thank those two respondants to my post, and I hope that they don't 
mind my sharing their information with others in this newsgroup.

Mort Gale.





From owner-ageing@net.bio.net Mon Jul 24 23:00:00 1995
Newsgroups: bionet.molbio.ageing
Path: biosci!lhc!nih-csl!NewsWatcher!user
From: Stauffer@codon.nih.gov (Jim Stauffer)
Subject: Symposium: Molecular Mechanisms Regulating Skeletal Muscle Plasticity
Message-ID: <Stauffer-2407951053080001@128.231.222.63>
Sender: postman@alw.nih.gov (AMDS Postmaster)
Nntp-Posting-Host: 128.231.222.63
Organization: UMN/LDN/NIHCD/NIH
Date: Mon, 24 Jul 1995 15:53:08 GMT
Lines: 43

Please post or pass along the following announcement:


                       SYMPOSIUM                             

MOLECULAR MECHANISMS REGULATING SKELETAL MUSCLE PLASTICITY


September 24-27, 1995; Airlie Conference Center, Airlie, VA.
Sponsored by NICHD, NIH.


Sessions & speakers will include:

MYOBLAST AND MYOFIBRIL  DIVERSITY
     C. Ordahl, B. Wold, N. Rosenthal, L. Leinwand

DETERMINATION AND  DIFFERENTIATION FACTORS 
     E. Olson, B. Paterson, W. Wright

SYNAPTOGENESIS AND PLASTICITY AT THE NMJ 
     J. Lichtman, W. Thompson, S. Burden, Z. Hall

MECHANISMS REGULATING FIBER-TYPE PLASTICITY
     D. Pette, A. Kelly, S. Williams, S. Hauschka,
     S. Schiaffino, A. Buonanno

REGENERATION AND NEUROMUSCULAR DISESASE
     M. Rudnicki, Z. Yablonka-Reuveni, H. Blau


Limited to 150 people.  Registration deadline is August 15, 1995.
For information on registration and poster sessions contact:

Andres Buonanno, Maxine Schaefer or Georgia Schwartz
Muscle Plasticity Symposium
Building 49, Room 5A-38
NIH, 49 Convent Drive
Bethesda, MD  20892-4480

Phone (301) 496-1463
Fax (301) 496-9939
E-Mail: buonanno@helix.nih.gov

From owner-ageing@net.bio.net Mon Jul 24 23:00:00 1995
Path: biosci!bcm!cs.utexas.edu!swrinde!howland.reston.ans.net!news-e1a.megaweb.com!newstf01.news.aol.com!newsbf02.news.aol.com!not-for-mail
From: tristan314@aol.com (Tristan314)
Newsgroups: bionet.molbio.ageing
Subject: Re: Looking for Novel Therapeutic Proteins for Licensing
Date: 23 Jul 1995 15:55:00 -0400
Organization: America Online, Inc. (1-800-827-6364)
Lines: 2
Sender: root@newsbf02.news.aol.com
Message-ID: <3uu9ek$b7q@newsbf02.news.aol.com>
References: <kathylee.8.300E4CD7@yorku.ca>
Reply-To: tristan314@aol.com (Tristan314)
NNTP-Posting-Host: newsbf02.mail.aol.com

I, too, am looking for any free information that would make me rich!
;-)

From owner-ageing@net.bio.net Sun Jul 30 23:00:00 1995
Path: biosci!daresbury!nntp-trd.UNINETT.no!Norway.EU.net!EU.net!howland.reston.ans.net!news.sprintlink.net!uunet!in2.uu.net!hoho.quake.net!xdcrlab.com!user
From: xdcrlab@quake.net (Mike Davis)
Newsgroups: bionet.molbio.ageing
Subject: Re: Melatonin Dosage II
Date: Mon, 31 Jul 1995 08:01:42 -0700
Organization: XdcrLab
Lines: 13
Message-ID: <xdcrlab-3107950801420001@xdcrlab.com>
References: <mortgale.13.3013EF6E@omni.voicenet.com>
NNTP-Posting-Host: xdcrlab.com
X-Newsreader: Value-Added NewsWatcher 2.0b24.0+

In article <mortgale.13.3013EF6E@omni.voicenet.com>,
mortgale@omni.voicenet.com (Morten Gale) wrote:

> WWW Sites:  http://pharminfo.com;   http:www.usc.edu/dept/nbio/nibs.html; and 
> http://www.hookup.net/mall/aging/agesit59.html.
>
The VRP melatonin articles are available on my website as is a link to the
LEF website and their articles.

-- 
Mike Davis  (((  xdcrlab@quake.net  )))   (((  Ultrasonic Devices  )))
Discnt.Suppl.List;Articles: http://www.quake.net/~xdcrlab/hp.html
Ultrasnd.Tchnlgy: http://www.quake.net/~xdcrlab/Ultrasound.html

