Cited by 26Receptor Mechanisms and SignalingProtein Kinase Regulation and GTPase SignalingPhosphodiesterase function and regulation

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

Morgan, Noel G., Shipp, Clanton C., Exton, John H.·1983·FEBS Letters

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 Ca 2+‐depleted hepatocytes. Half‐maximal inhibition of cAMP accumulation occurred at 8 × 10‐11 M vasopressin, a dose which does not increase cytosolic Ca 2+ in hepatocytes. Direct activation of adenylate cyclase by forskolin was significantly inhibited by vasopressin in Ca 2+‐depleted cells. It is concluded that inhibition of hormone‐induced cAMP accumulation by vasopressin in liver is not dependent on cellular Ca 2+ mobilisation but may involve direct inhibition of adenylate cyclase.

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Crossref · 10.1016/0014-5793(83)80835-7

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19 of 19 references verified0 citation errors · 0 not checkable

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Authors
Morgan, N. G., Shipp, C. C., & Exton, J. H.
Affiliations
Howard Hughes Medical Institute (US)
Venue
FEBS Letters
Publisher
Wiley
Published
1983-11-14
Volume
163
Issue
2
Pages
277-281
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W1967615830
Cited by
26
References
19
Citations by year
2017: 1 · 2015: 1
FWCI
0.79
Type
journal article
Language
en
Open access
closed
Locations
  • FEBS Letters (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Phosphodiesterase function and regulation
Keywords
vasopressin, cAMP accumulation, hepatocytes, glucagon, adenylate cyclase inhibition, calmodulin, calcium depletion, forskolin, liver
MeSH terms
Cyclic AMP, Adenylyl Cyclases, Animals, Calcium, Calmodulin, Chlorpromazine, Diterpenes, Dose-Response Relationship, Drug, Enzyme Activation, Colforsin, Glucagon, Liver, Male, Rats, Inbred Strains, Trifluoperazine, Vasopressins, Rats, In Vitro Techniques

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