CENTRAL EFFECTS OF MUSCARINIC AGONISTS AND ANTAGONISTS ON HIPPOCAMPAL THETA-RHYTHM AND BLOOD-PRESSURE IN THE ANESTHETIZED RAT

被引:24
作者
BARNES, JC
ROBERTS, FF
机构
[1] Department of Neuropharmacology, Glaxo Group Research Ltd., Ware, Hertfordshire SG12 ODP, Park Road
关键词
THETA-RHYTHM; BLOOD PRESSURE; MUSCARINIC RECEPTOR AGONISTS; MUSCARINIC RECEPTOR ANTAGONISTS; MUSCARINIC RECEPTOR SUBTYPES; (RAT);
D O I
10.1016/0014-2999(91)90540-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The in vivo central effects of a range of full and partial muscarinic receptor agonists have been investigated on hippocampal theta rhythm and blood pressure. In the isoflurane-anaesthetised rat, pretreated with N-methylscopolamine, i.v. administration of arecoline, oxotremorine, arecaidine propargly ester, acelidine and pilocarpine produced dose-dependent increases in the frequency of hippocampal theta rhythm and blood pressure, with an order of potency of arecoline = oxotremorine = arecaidine propargyl ester > aceclidine greater-than-or-equal-to pilocarpine. To increase theta wave frequency, pilocarpine showed a low maximum response and possessed antagonist activity against arecoline, indicating that pilocarpine was acting as a partial agonist. AF102B failed to alter blood pressure or theta rhythm. Intraventricular injections of scopolamine and the M1 receptor-selective antagonist, pirenzepine, produced dose-dependent antagonism of the enhanced theta wave frequency and hypertensive response produced by arecoline. The differences in antagonist potency for the two responses was less than 6-fold, which indicated that both the increase in hippocampal theta wave activity and increase in blood pressure may have been mediated through muscarinic receptors of the M1 subtype. Further studies using a wider range of antagonists will be required to confirm this conclusion.
引用
收藏
页码:233 / 240
页数:8
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