Abstract
The effects of Ca2+-calmodulin on adenylate cyclase activity in EGTA-washed, 27000 g particulate fractions of mouse and rat pancreatic islets were studied. Ca2+ (10 microM)-calmodulin (1 microM) stimulated adenylate cyclase activity 53.1 +/- 5.2 (N = 6)% in the particulate fraction of rat islets. Trifluoperazine (50 microM), a specific inhibitor of calmodulin, inhibited the Ca2+-calmodulin activation of the adenylate cyclase activity of this fraction of rat islets. These results confirm previous reports dealing with Ca2+-Calmodulin and rat islet adenylate cyclase [Valverde, Vandermeers. Anjaneyulu & Malaisse (1979) Science 206, 225-227; Sharp, Wiedenkeller, Kaelin, Siegel & Wollheim (1980) Diabetes 29, 74-77]. In contrast, however, Ca2+ (1-100 microM)-calmodulin (1-10 microM) did not stimulate the adenylate cyclase activity in the EGTA-washed particulate fraction of mouse islets, and trifluoperazine (50 microM) did not inhibit the adenylate cyclase activity of this fraction of mouse islets, although some remaining calmodulin [0.18 +/- 0.05 (n = 3) microgram/mg of protein] could be demonstrated. GTP (10 microM) enhanced islet adenylate cyclase activity considerably, but did not confer any sensitivity towards Ca2+-calmodulin on mouse islet adenylate cyclase. The results question the role of calmodulin in the Ca2+-dependent rise in cyclic AMP evoked by glucose in pancreatic islets.
MeSH Terms
Adenylyl Cyclases/metabolism
Animals
Calcium/pharmacology
Calcium-Binding Proteins/pharmacology
Calmodulin/pharmacology
Dose-Response Relationship, Drug
Enzyme Activation/drug effects
Guanosine Triphosphate/pharmacology
In Vitro Techniques
Islets of Langerhans/drug effects,enzymology
Male
Mice
Rats
Species Specificity
Trifluoperazine/pharmacology
Chemicals
Calcium-Binding Proteins
Calmodulin
Trifluoperazine
Guanosine Triphosphate
Adenylyl Cyclases
Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Thams P
Capito K
Hedeskov C J
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