Gil, D W

Pirenzepine distinguishes between muscarinic receptor-mediated phosphoinositide breakdown and inhibition of adenylate cyclase. [electronic resource] - The Journal of pharmacology and experimental therapeutics Mar 1985 - 608-16 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.

0022-3565


(4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium Chloride--pharmacology
Acetylcholine--pharmacology
Adenylyl Cyclase Inhibitors
Animals
Atropine--pharmacology
Benzodiazepinones--pharmacology
Brain--metabolism
Carbachol--pharmacology
In Vitro Techniques
Inositol--analogs & derivatives
Inositol Phosphates
Male
Myocardium--metabolism
Oxotremorine--pharmacology
Parotid Gland--metabolism
Phosphatidylinositols--metabolism
Pirenzepine
Quinuclidinyl Benzilate--metabolism
Radioligand Assay
Rats
Rats, Inbred Strains
Receptors, Muscarinic--drug effects