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H2受体阻断对大鼠前列环素某些中枢效应的影响。

Influence of H2 receptors blockade upon some central effects of prostacyclin in rats.

作者信息

Brus R, Krzemiński T, Juraszczyk Z, Kurcok A, Felińska W

出版信息

Pol J Pharmacol Pharm. 1985 Nov-Dec;37(6):831-9.

PMID:2870486
Abstract

Prostacyclin (PGI2) administered icv into the lateral rat brain ventricle in a dose of 1 and 10 micrograms caused hypothermia and catalepsy. Joint administration of PGI2 and chlorpromazine produced a greater cataleptic effect than that observed after the neuroleptic alone. Cimetidine (CMT) 2 g/kg po administered 60 min before PGI2 icv injection inhibited hypothermic and cataleptogenic action of PGI2. CMT blocked the cataleptogenic effect of chlorpromazine as well as combination of it with PGI2. CMT inhibited cataleptogenic effect of haloperidol, but it did not block the catalepsy induced by joint administration of haloperidol and PGI2. PGI2 did not change concentration of noradrenaline and dopamine in different brain areas. The results indicate that H2 receptors take part in some central pharmacological effects of PGI2 in rats.

摘要

将剂量为1微克和10微克的前列环素(PGI2)脑室内注射到大鼠侧脑室会引起体温过低和僵住症。PGI2与氯丙嗪联合给药产生的僵住症效应比单独使用该抗精神病药物时更明显。在脑室内注射PGI2前60分钟口服2克/千克西咪替丁(CMT)可抑制PGI2的体温过低和致僵住症作用。CMT可阻断氯丙嗪以及氯丙嗪与PGI2联合用药的致僵住症效应。CMT可抑制氟哌啶醇的致僵住症效应,但它不能阻断氟哌啶醇与PGI2联合给药所诱导的僵住症。PGI2不会改变不同脑区去甲肾上腺素和多巴胺的浓度。结果表明,H2受体参与了PGI2在大鼠中的某些中枢药理作用。

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