Characterization of the mechanism of action of tachykinins in rat striatal cholinergic interneurons

被引:32
作者
Bell, MI
Richardson, PJ
Lee, K
机构
[1] Parke Davis Neurosci Res Ctr, Cambridge, England
[2] MRC, Cambridge Ctr Brain Repair, Cambridge, England
[3] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QJ, England
关键词
striatum; tachykinins; acetylcholine;
D O I
10.1016/S0306-4522(98)00187-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mechanism by which substance P depolarizes cholinergic interneurons in the rat striatum was studied using whole-cell recording techniques. In all cases the effects of substance P were mimicked by the neurokinin(1) receptor agonist [Sar(9), Met(O-2)(11)] substance P and were antagonized by the neurokinin(1) receptor antagonist SR 140333. [Sarg(9) Met(O-2)(11)] substance P was found to depolarize cholinergic interneurons by the induction of a calcium-activated inward current at - 60 mV. This inward current was irreversibly potentiated by photolysis of caged GTP gamma S within neurons implicating the involvement of a G-protein. The [Sarg(9) Met(O-2)(11)] substance P-induced inward current was inhibited by the phospholipase C inhibitor U-73122, and by the inclusion of the inositol-1,4.5-triphosphate receptor antagonist heparin in the electrode solution. These findings suggest that neurokinin(1) receptors depolarize cholinergic interneurons in the rat striatum primarily through a phosphoinositide signalling pathway. (C) 1998 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:649 / 658
页数:10
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