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在大鼠中,西咪替丁可减弱促甲状腺激素释放激素(TRH)的心血管效应。

The cardiovascular effects of thyrotropin-releasing hormone (TRH) are attenuated by cimetidine in rats.

作者信息

Nurminen M L, Paakkari I, Jrvinen A, Vonhof S

机构信息

Department of Pharmacology and Toxicology, University of Helsinki, Finland.

出版信息

Pharmacol Toxicol. 1991 Nov;69(5):322-6. doi: 10.1111/j.1600-0773.1991.tb01304.x.

Abstract

The modulation of cardioventilator effects of thyrotropin-releasing hormone (TRH) by histaminergic mechanisms was studied in anaesthetized rats pretreated with histamine receptor antagonists. TRH (1-100 nmol/kg) into the lateral cerebral ventricle dose-dependently elevated mean arterial pressure, heart rate and stimulated respiration. The respiratory stimulating effect of TRH remained unchanged after pretreatments with histamine H1-receptor antagonist diphenhydramine or H2-receptor antagonists cimetidine and ranitidine, while the TRH-induced hypertension and tachycardia were attenuated by cimetidine. This antagonism was not due to an interaction between TRH and cimetidine at their central binding sites, since there was no displacement of [3H]MeTRH binding in the presence of cimetidine nor did TRH displace [3H]cimetidine in rat brain homogenates. Inability of diphenhydramine to modify the cardiovascular effects of TRH indicates that these effects are not due to histamine liberation, as cardiovascular stimulation after central administration of histamine is mainly mediated via H1-receptors. The antagonism of the cardiovascular responses to TRH by cimetidine was not due to blockade of H2-receptors, since another potent H2-receptor antagonist ranitidine was unable to affect the cardiovascular effects of TRH. Therefore, we suggest that cimetidine exerted antagonism of TRH by some non-specific action.

摘要

在预先用组胺受体拮抗剂处理的麻醉大鼠中,研究了组胺能机制对促甲状腺激素释放激素(TRH)心血管呼吸作用的调节。向侧脑室注射TRH(1-100 nmol/kg)可剂量依赖性地升高平均动脉压、心率并刺激呼吸。在用组胺H1受体拮抗剂苯海拉明或H2受体拮抗剂西咪替丁和雷尼替丁预处理后,TRH的呼吸刺激作用保持不变,而西咪替丁可减弱TRH诱导的高血压和心动过速。这种拮抗作用并非由于TRH与西咪替丁在其中心结合位点的相互作用,因为在西咪替丁存在的情况下,[3H]MeTRH结合没有被取代,并且在大鼠脑匀浆中TRH也没有取代[3H]西咪替丁。苯海拉明不能改变TRH的心血管作用,这表明这些作用不是由于组胺释放,因为中枢给予组胺后的心血管刺激主要通过H1受体介导。西咪替丁对TRH心血管反应的拮抗作用不是由于H2受体的阻断,因为另一种强效H2受体拮抗剂雷尼替丁不能影响TRH的心血管作用。因此,我们认为西咪替丁通过一些非特异性作用对TRH产生拮抗作用。

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