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伏隔核内注射组胺对大鼠自发运动活动的双相作用;中枢组胺受体的作用

Biphasic effects of intra-accumbens histamine administration on spontaneous motor activity in the rat; a role for central histamine receptors.

作者信息

Bristow L J, Bennett G W

机构信息

Department of Physiology and Pharmacology, Medical School, Queen's Medical Centre, Nottingham.

出版信息

Br J Pharmacol. 1988 Dec;95(4):1292-302. doi: 10.1111/j.1476-5381.1988.tb11767.x.

Abstract
  1. The effect of intra-accumbens injection of histamine and related compounds on the spontaneous motor activity of the rat has been investigated. 2. Microinjections of histamine (1-200 micrograms) induced dose-dependent, biphasic changes in rat activity consisting of an initial brief hypoactivity response followed by a marked hyperactivity phase. The histamine metabolite, n-tele-methylhistamine was without effect. 3. Pretreatment with the H1-receptor antagonist mepyramine (10 micrograms) blocked the hypoactivity response and markedly attenuated histamine-induced hyperactivity. In contrast, pretreatment with the H2-receptor antagonist SKF93479 had no effect on histamine-induced behaviour. 4. Microinjection of the H1-receptor agonist 2-thiazolylethylamine induced a marked hyperactivity response, but unlike the response to histamine, there was no initial hypoactivity. The H2-receptor agonist dimaprit had no apparent behavioural effects following intra-accumbens injection. 5. Intra-accumbens injection of the non-selective histamine agonists n alpha-methylhistamine or n alpha, n alpha-dimethylhistamine induced both marked hypoactivity and hyperactivity responses which were comparable with the effects of histamine. 6. The present results demonstrate a histamine, H1-receptor-mediated arousal in the nucleus accumbens which follows transitory hypoactivity, possibly due to activation of presynaptic H3-receptors.
摘要
  1. 研究了向伏隔核注射组胺及相关化合物对大鼠自发运动活动的影响。2. 微量注射组胺(1 - 200微克)可引起大鼠活动呈剂量依赖性的双相变化,先是短暂的活动减少反应,随后是明显的活动亢进阶段。组胺代谢产物N - 甲基组胺无此作用。3. 用H1受体拮抗剂美吡拉敏(10微克)预处理可阻断活动减少反应,并显著减弱组胺诱导的活动亢进。相反,用H2受体拮抗剂SKF93479预处理对组胺诱导的行为无影响。4. 微量注射H1受体激动剂2 - 噻唑基乙胺可引起明显的活动亢进反应,但与对组胺的反应不同,没有初始的活动减少。向伏隔核注射H2受体激动剂二甲双胍后没有明显的行为效应。5. 向伏隔核注射非选择性组胺激动剂Nα - 甲基组胺或Nα,Nα - 二甲基组胺可引起明显的活动减少和活动亢进反应,这与组胺的作用相当。6. 目前的结果表明,伏隔核中存在由组胺、H1受体介导的觉醒,在短暂的活动减少之后出现,这可能是由于突触前H3受体的激活所致。

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