CAMP REGULATION OF VASOPRESSIN MESSENGER-RNA CONTENT IN HYPOTHALAMONEUROHYPOPHYSEAL EXPLANTS

Citation
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
Citations number
27
Categorie Soggetti
Physiology
ISSN journal
03636119
Volume
40
Issue
3
Year of publication
1996
Pages
554 - 560
Database
ISI
SICI code
0363-6119(1996)40:3<554:CROVMC>2.0.ZU;2-I
Abstract
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.