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内源性阿片系统与二氢吡啶诱导的大鼠交感神经张力的中枢调节

Endogenous opiate system and dihydropyridine-induced central regulation of sympathetic tone in rats.

作者信息

Champeroux P, Brisac A M, Laurent S, Schmitt H

机构信息

Centre de Recherches Biologiques, Baugy, France.

出版信息

Eur J Pharmacol. 1988 Dec 6;158(1-2):157-60. doi: 10.1016/0014-2999(88)90267-1.

Abstract

Intracerebroventricular injections of nicardipine (10 micrograms/kg) to SHR induced hypotension which was suppressed by pretreatment with 6-OHDA. This hypotension was also inhibited by a previous injection of naloxone (100 micrograms/kg i.c.v.) whereas the hypotension induced by intravenously injected nicardipine (10 micrograms/kg) was not changed. It is suggested that the release of endogenous opioids is involved in the sympatho-inhibitory effect of centrally administered dihydropyridine calcium channel antagonists.

摘要

向自发性高血压大鼠(SHR)脑室内注射硝苯地平(10微克/千克)可诱导低血压,而用6-羟基多巴胺(6-OHDA)预处理可抑制这种低血压。预先注射纳洛酮(100微克/千克,脑室内注射)也可抑制这种低血压,而静脉注射硝苯地平(10微克/千克)所诱导的低血压则没有变化。这表明内源性阿片类物质的释放参与了中枢给予二氢吡啶类钙通道拮抗剂的交感抑制作用。

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