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向大鼠前扣带回皮质微量注射组胺对福尔马林诱导的疼痛相关行为的影响。

Effects of microinjection of histamine into the anterior cingulate cortex on pain-related behaviors induced by formalin in rats.

作者信息

Hamzeh-Gooshchi Nasrin, Tamaddonfard Esmaeal, Farshid Amir Abbas

机构信息

Division of Physiology, Department of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.

Division of Physiology, Department of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.

出版信息

Pharmacol Rep. 2015 Jun;67(3):593-9. doi: 10.1016/j.pharep.2014.12.019. Epub 2015 Jan 15.

Abstract

BACKGROUND

The present study was aimed to investigate the effects of microinjection of histamine and its H1, H2 and H3 receptor antagonists, mepyramine, ranitidine and thioperamide, respectively, into the anterior cingulate cortex (ACC) on pain-related behaviors induced by formalin in rats.

METHODS

Two stainless steel guide canulas were bilaterally implanted into the ACC of anaesthetized rats. For induction of pain, intraplantar (ipl) injection of a 2.5% formalin solution was performed. The duration of paw licking/biting and the number of paw flinching were recorded in 5 min blocks for 60 min. Locomotor activity was assessed using an open-field test.

RESULTS

Formalin produced a marked biphasic pattern of pain. Histamine reduced the second phases of paw licking/biting and flinching. Mepyramine (2 μg/side) prevented the suppressive effect of histamine (1 μg/side) on second phase of pain, but at a dose of 8 μg/side it did not inhibit the suppressive effects of 4 μg/side of histamine. Ranitidine at doses of 2 and 8 μg/side prevented histamine (1 and 4 μg/side)-induced antinociception. Thioperamide not only suppressed the second phases of pain, but also increased the suppressive effect of histamine. Naloxone prevented suppressive effects of histamine and thioperamide on pain. Mepyramine (8 μg/side) suppressed locomotor activity.

CONCLUSION

The results of the present study showed pain suppressing effects for histamine. Histamine H2 and H3, and to a lesser extent, H1 receptors might be involved in histamine-induced antinociception. Opioid receptors might be involved in suppressive effects of histamine and thioperamide.

摘要

背景

本研究旨在探讨分别向大鼠前扣带回皮质(ACC)微量注射组胺及其H1、H2和H3受体拮抗剂美吡拉敏、雷尼替丁和硫代哌酰胺对福尔马林诱导的疼痛相关行为的影响。

方法

将两根不锈钢引导套管双侧植入麻醉大鼠的ACC。为诱导疼痛,进行足底(ipl)注射2.5%福尔马林溶液。在60分钟内以5分钟为时间段记录舔足/咬足持续时间和足部退缩次数。使用旷场试验评估运动活动。

结果

福尔马林产生明显的双相疼痛模式。组胺减少了舔足/咬足和退缩的第二阶段。美吡拉敏(2μg/侧)可防止组胺(1μg/侧)对疼痛第二阶段的抑制作用,但在剂量为8μg/侧时,它并不抑制4μg/侧组胺的抑制作用。雷尼替丁在2μg/侧和8μg/侧剂量下可防止组胺(1μg/侧和4μg/侧)诱导的镇痛作用。硫代哌酰胺不仅抑制疼痛的第二阶段,还增强了组胺的抑制作用。纳洛酮可防止组胺和硫代哌酰胺对疼痛的抑制作用。美吡拉敏(8μg/侧)抑制运动活动。

结论

本研究结果显示组胺具有疼痛抑制作用。组胺H2和H3受体,以及程度较轻的H1受体可能参与组胺诱导的镇痛作用。阿片受体可能参与组胺和硫代哌酰胺的抑制作用。

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