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Molecular Pharmacology, Vol 6, 184-188, Copyright © 1970 by the American Society for Pharmacology and Experimental Therapeutics
1 National Institute of Arthritis and Metabolic Diseases, National Institutes of Health,
Bethesda, Maryland 20014
The formation of cyclic adenosine 3',5'-monophosphate-14C from endogenous ATP-14C is greatly stimulated on incubation of cerebral cortex slices with depolarizing agents such as batrachotoxin, veratridine, ouabain, and potassium ion. In slices of cerebral cortex, batrachotoxin is the most potent known stimulant (ED50 = 1 x 10-7 M) of cyclic 3',5'-AMP-14C formation. Stimulation of cyclic 3',5'-AMP-14C formation by depolarizing agents requires calcium ions and is inhibited by theophylline. Stimulation of cyclic 3',5'-AMP-14C formation by histamine, in contrast, does not require calcium ions and is not inhibited by theophylline. The results suggest a relationship among depolarization, transmitter release, and cyclic 3',5'-AMP formation in brain.
Submitted on January 10, 1970
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