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向齿状回内微量注射组织胺可在大鼠福尔马林试验中产生抗伤害作用。

Microinjection of histamine into the dentate gyrus produces antinociception in the formalin test in rats.

机构信息

Division of Physiology, Department of Basic Sciences, Faculty of Veterinary Medicine, P.O. Box 1177, Urmia University, Urmia 57135, Iran.

出版信息

Pharmacol Biochem Behav. 2010 Dec;97(2):325-32. doi: 10.1016/j.pbb.2010.08.018. Epub 2010 Sep 6.

Abstract

The present study was aimed to investigate the effects of microinjection of histamine, chlorpheniramine (a histamine H(1) receptor antagonist), ranitidine (a histamine H(2) receptor antagonist) and thioperamide (a histamine H(3) receptor antagonist) into the dentate gyrus on the formalin-induced pain. A biphasic pattern (first phase: 0-5min and second phase: 15-60min) in nociceptive responses was induced after subcutaneous injection of formalin (50μl, 2.5%) into the ventral surface of the right hind paw. Microinjection of histamine (1 and 2μg) into the dentate gyrus decreased the intensity of nociceptive responses. Intra-dentate gyrus microinjection of chlorpheniramine and ranitidine at the same doses of 1 and 4μg had no effects, whereas thioperamide at a dose of 4μg suppressed both phases of formalin-induced pain. Pretreatments with chlorpheniramine and ranitidine at the same dose of 4μg prevented histamine (2μg)-induced antinociception, while thioperamide (4μg) increased histamine (2μg)-induced antinociception. These results indicated that activation of brain neuronal histamine at the levels of dentate gyrus produced antinociception. The post-synaptic H(1), H(2) receptors and pre-synaptic H(3) receptors of histamine may be involved in the histamine-induced antinociception at the level of the dentate gyrus.

摘要

本研究旨在探讨向齿状回内微量注射组胺、氯苯那敏(组胺 H1 受体拮抗剂)、雷尼替丁(组胺 H2 受体拮抗剂)和噻哌酰胺(组胺 H3 受体拮抗剂)对福尔马林诱导疼痛的影响。福尔马林(50μl,2.5%)皮下注射到右后爪腹面后,会引起痛觉反应的双相模式(第一相:0-5min;第二相:15-60min)。向齿状回内微量注射组胺(1 和 2μg)可降低痛觉反应的强度。向齿状回内微量注射氯苯那敏和雷尼替丁(剂量为 1 和 4μg)没有效果,但噻哌酰胺(4μg)抑制了福尔马林诱导的疼痛的两个阶段。预先给予相同剂量(4μg)的氯苯那敏和雷尼替丁可预防组胺(2μg)引起的镇痛,而噻哌酰胺(4μg)则增强了组胺(2μg)引起的镇痛。这些结果表明,齿状回水平的脑神经元组胺的激活产生了镇痛作用。组胺诱导的齿状回镇痛可能涉及突触后 H1、H2 受体和突触前 H3 受体。

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