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Forskolin: a specific stimulator of adenylyl cyclase or a diterpene with multiple sites of action?

Authors :
Laurenza A
Sutkowski EM
Seamon KB
Source :
Trends in pharmacological sciences [Trends Pharmacol Sci] 1989 Nov; Vol. 10 (11), pp. 442-7.
Publication Year :
1989

Abstract

Forskolin, a naturally occurring diterpene, directly stimulates adenylyl cyclase and has been used extensively to increase cAMP and to elicit cAMP-dependent physiological responses. More recently, forskolin has been shown to inhibit a number of membrane transport proteins and channel proteins through a mechanism that does not involve the production of cAMP. Many of these channel proteins are predicted to have similar topographies in the membrane bilayer and it is tempting to speculate that forskolin may be binding at structurally homologous sites. Kenneth Seamon and colleagues discuss the cAMP-independent effects of forskolin and the structural similarity between forskolin and other physiologically important substances such as hexoses and steroids with respect to potential forskolin binding sites.

Details

Language :
English
ISSN :
0165-6147
Volume :
10
Issue :
11
Database :
MEDLINE
Journal :
Trends in pharmacological sciences
Publication Type :
Academic Journal
Accession number :
2692256
Full Text :
https://doi.org/10.1016/S0165-6147(89)80008-2