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L-组氨酸和异丙嗪对大鼠阿扑吗啡和金刚烷胺刻板行为的影响。

Effects of L-histidine and promethazine on apomorphine and amantadine stereotypy in rats.

作者信息

Balsara J J, Dhavare B S, Nandal N V, Chandorkar A G

出版信息

Psychopharmacology (Berl). 1983;79(4):372-4. doi: 10.1007/BF00433422.

Abstract

Pretreatment with L-histidine, a precursor of brain histamine, and promethazine, a H1 receptor blocker, failed to modify apomorphine-induced stereotyped behaviour in rats. In contrast, pretreatment with L-histidine significantly decreased the intensity of amantadine stereotypy while pretreatment with promethazine significantly increased the intensity of amantadine stereotypy in rats. The results suggest that drugs which influence central histaminergic mechanisms are effective only in modifying the stereotyped behaviour induced by the indirectly-acting DA agonist amantadine, and fail to modify the stereotyped behaviour induced by apomorphine, a directly-acting DA agonist.

摘要

用L-组氨酸(一种脑内组胺的前体)和异丙嗪(一种H1受体阻滞剂)进行预处理,未能改变阿扑吗啡诱导的大鼠刻板行为。相反,用L-组氨酸预处理可显著降低金刚烷胺刻板行为的强度,而用异丙嗪预处理则可显著增加大鼠金刚烷胺刻板行为的强度。结果表明,影响中枢组胺能机制的药物仅对改变间接作用的多巴胺激动剂金刚烷胺诱导的刻板行为有效,而对直接作用的多巴胺激动剂阿扑吗啡诱导的刻板行为无效。

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