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RU 24969诱导大鼠运动是由5-羟色胺1A受体介导的。

RU 24969-induced locomotion in rats is mediated by 5-HT1A receptors.

作者信息

Kalkman H O

机构信息

Sandoz Pharma, Basel, Switzerland.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1995 Nov;352(5):583-4. doi: 10.1007/BF00169395.

Abstract

The locomotor response to RU 24969 (5-methoxy-3-(1,2,3,6-tetrahydropyridin-4-yl) 1H-indole; 10 mg/kg, s.c.), a preferential 5-HT(1B) receptor agonist, was investigated in the rat, using two novel 5-HT(1A) receptor antagonists, WAY-100635 (0.3 mg/kg and 1 mg/kg, s.c.) and SDZ 216-525 (0.3 mg/kg, s.c.), and the novel 5-HT(1B)/5-HT(1D) receptor antagonist, GR 127935 (1 mg/kg, s.c.). The antagonists per se did not alter spontaneous locomotion. Both selective 5-HT(1A) receptor antagonists blocked RU 24969-induced hyperlocomotion, whilst the 5-HT(1B) receptor antagonist was without effect. These results suggest that RU 24969-induced hyperlocomotion in the rat is mediated by 5-HT(1A) receptors.

摘要

使用两种新型5-HT(1A)受体拮抗剂WAY-100635(0.3毫克/千克和1毫克/千克,皮下注射)和SDZ 216-525(0.3毫克/千克,皮下注射)以及新型5-HT(1B)/5-HT(1D)受体拮抗剂GR 127935(1毫克/千克,皮下注射),在大鼠中研究了对RU 24969(5-甲氧基-3-(1,2,3,6-四氢吡啶-4-基)1H-吲哚;10毫克/千克,皮下注射)的运动反应,RU 24969是一种选择性5-HT(1B)受体激动剂。这些拮抗剂本身不会改变自发运动。两种选择性5-HT(1A)受体拮抗剂均能阻断RU 24969诱导的运动亢进,而5-HT(1B)受体拮抗剂则无此作用。这些结果表明,RU 24969诱导的大鼠运动亢进是由5-HT(1A)受体介导的。

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