Cd. Sladek et al., CAMP REGULATION OF VASOPRESSIN MESSENGER-RNA CONTENT IN HYPOTHALAMONEUROHYPOPHYSEAL EXPLANTS, American journal of physiology. Regulatory, integrative and comparative physiology, 40(3), 1996, pp. 554-560
Stimulation of vasopressin (VP) gene expression by adenosine 3',5'-cyc
lic monophosphate (cAMP) has been observed in dispersed hypothalamic c
ultures, in VP-expressing cell lines, and in cells transfected with re
porter genes regulated by the VP gene promoter. However, treatment of
hypothalamo-neurohypophysial system (HNS) explants with forskolin (25
mu M), an activator of adenyl cyclase, and 3-isobutyl-1-methylxanthine
(IBMX; 500 mu M), a phosphodiesterase inhibitor, resulted in a decrea
se in VP mRNA. Time course analysis revealed that IBMX and forskolin r
educed the VP mRNA content to 50% of control explants after 8 and 12 h
despite a dramatic stimulation of VP release. This effect was due to
the activation of adenyl cyclase by forskolin, because neither IBMX al
one nor the inactive analogue of forskolin, 1,9-dideoxyforskolin, decr
eased VP mRNA content. In contrast, 8-bromoadenosine 3',5'-cyclic mono
phosphate and the D-1 dopamine receptor agonist, SKF-38393, increased
VP mRNA content, but these agents were less potent in stimulating VP r
elease, suggesting a concentration dependency of the forskolin effect.
This was confirmed when forskolin (10 mu M) was found to increase VP
mRNA content. Thus receptor-mediated activation of adenyl cyclase resu
lts in an increase in VP mRNA content.