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[在5-羟色胺能和γ-氨基丁酸能过程激活背景下调节吗啡镇痛作用的可能性]

[Possibility of modulating morphine analgesia against a background of activation of serotonin- and GABA-ergic processes].

作者信息

Andreev B V, Vasil'ev Iu N, Ignatov Iu D

出版信息

Farmakol Toksikol. 1981 Jan-Feb;44(1):34-7.

PMID:6973490
Abstract

The analgesic effect of morphine in conditions of serotonin- and GABA-ergic activation was studied in experiments on male albino rats. The serotonin re-uptake blockers fluoxetin and citalopram (10 and 20 mg/kg) did not exert clear analgesic effect or did not potentiate morphine action in doses of 5 and 10 mg/kg. The GABA agonist muscimol (0.5--2 mg/kg) did not influence the pain reaction structure and did not enhance morphine-induced analgesia. The role of serotonin- and GABA-ergic processes in realization of the analgesic action of morphine is discussed.

摘要

在雄性白化大鼠实验中研究了吗啡在血清素和γ-氨基丁酸能激活情况下的镇痛作用。血清素再摄取阻滞剂氟西汀和西酞普兰(10和20毫克/千克)未产生明显镇痛效果,或在5和10毫克/千克剂量下未增强吗啡作用。γ-氨基丁酸激动剂蝇蕈醇(0.5 - 2毫克/千克)未影响疼痛反应结构,也未增强吗啡诱导的镇痛作用。讨论了血清素和γ-氨基丁酸能过程在吗啡镇痛作用实现中的作用。

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