Studies on the mechanism of inhibition of hepatic cAMP accumulation by vasopressin.

Abstract:

:Vasopressin elicited a dose-dependent inhibition of glucagon-induced cAMP accumulation in isolated hepatocytes. This response was not diminished by incubation of cells with the calmodulin antagonists trifluoperazine or chlorpromazine and was only slightly reduced in Ca2+-depleted hepatocytes. Half-maximal inhibition of cAMP accumulation occurred at 8 X 10(-11) M vasopressin, a dose which does not increase cytosolic Ca2+ in hepatocytes. Direct activation of adenylate cyclase by forskolin was significantly inhibited by vasopressin in Ca2+-depleted cells. It is concluded that inhibition of hormone-induced cAMP accumulation by vasopressin in liver is not dependent on cellular Ca2+ mobilisation but may involve direct inhibition of adenylate cyclase.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Morgan NG,Shipp CC,Exton JH

doi

10.1016/0014-5793(83)80835-7

subject

Has Abstract

pub_date

1983-11-14 00:00:00

pages

277-81

issue

2

eissn

0014-5793

issn

1873-3468

pii

0014-5793(83)80835-7

journal_volume

163

pub_type

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