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Muscarinic receptors mediate direct inhibition of GABA release from rat striatal nerve terminals.

作者信息

Marchi M, Sanguineti P, Raiteri M

机构信息

Istituto di Farmacologia e Farmacognosia, Università degli Studi di Genova, Italy.

出版信息

Neurosci Lett. 1990 Aug 24;116(3):347-51. doi: 10.1016/0304-3940(90)90099-u.

Abstract

The effects of acetylcholine (ACh) on the depolarization-evoked release of [3H]gamma-aminobutyric acid ([3H]GABA) have been investigated using synaptosomes prepared from rat corpus striatum and depolarized by superfusion with 9 mM KCl. Acetylcholine inhibited the [3H]GABA overflow in a concentration-dependent manner. The maximal effect was about 50%. The IC50 value (concentration producing half-maximal effect) amounted to 1 microM, in the absence of acetylcholinesterase inhibitors. The effect of ACh on the K(+)-evoked [3H]GABA release was counteracted by the muscarinic receptor antagonist atropine, but not by the nicotinic receptor antagonist mecamylamine or by the selective M1 antagonist pirenzepine. The data show that muscarinic receptors with low affinity for pirenzepine are localized on GABAergic nerve endings in rat corpus striatum where they may directly inhibit the release of GABA.

摘要

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