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PMID: 2152883 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Angiotensin II stimulates angiotensinogen synthesis in hepatocytes by a pertussis toxin-sensitive mechanism.

FEBS letters ·Vol. 259 ·No. 2 ·1990-01-01 ·Pages 301-4

Klett C, Muller F, Gierschik P, Hackenthal E

Abstract

The role of intracellular messengers in the stimulatory effect of angiotensin II on angiotensinogen synthesis and secretion in hepatocytes was examined. Angiotensinogen secretion was not influenced by modulators of intracellular calcium (calmidazolium, A 23187, Bay K 8644, methoxamine). In contrast, agents decreasing intracellular cAMP (angiotensin II, guanfacine) stimulated, and those increasing cAMP (isoproterenol, glucagon, forskolin) depressed angiotensinogen secretion. An inverse relationship was also observed between cAMP and angiotensinogen mRNA. Pretreatment of hepatocytes with pertussis toxin abolished the stimulation by angiotensin II. It is concluded that angiotensin II-induced stimulation of angiotensinogen synthesis is initiated by inhibition of adenylate cyclase.

MeSH Terms
Adenylate Cyclase Toxin Angiotensin II/pharmacology Angiotensinogen/biosynthesis,genetics Animals Cells, Cultured Cyclic AMP/metabolism Glucagon/pharmacology Kinetics Leucine/metabolism Liver/drug effects,enzymology Male Pertussis Toxin RNA, Messenger/genetics Rats Rats, Inbred Strains Transcription, Genetic/drug effects Tritium Virulence Factors, Bordetella/pharmacology
Chemicals
Adenylate Cyclase Toxin RNA, Messenger Virulence Factors, Bordetella Tritium Angiotensinogen Angiotensin II Glucagon Cyclic AMP Pertussis Toxin Leucine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Klett C
Department of Pharmacology, University of Heidelberg, FRG.
Muller F
Gierschik P
Hackenthal E
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1990-01-01
Pages
301-4
Language
English
Region
England
NLM ID
0155157
Subset
IM
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