>> I think that kappa opioid receptors are belived to couple via pertussis
> toxin-sensitive Gi/Go proteins to the inhibition of calcium channels.
> Now, Gi can also inhibit adenylyl cyclase, and there is evidence that Go
> can do the same. So that could explain an inhibitory effect on [cAMP] by
> U69593.
>> AJW
>
Aren't 4 Ca++ 's required for maximal AC activity? If so, A receptor
that activates the adenylate cyclase via the inositol pathway could be
inhibited by a Ca++ channel blocker. ie:
Ligand --> receptor
| DAG
\/ | ???
Gp-prot-----> phospolipase c---->C-kinase------>Adeny-
| ^ late
\/ | Cyclase
IP3---ER--->Ca++ |
^ release-----|
|
U69593 (?)
Comments/criticisms appreciated
Chris