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单皮质扩散性抑制是否会引起自由活动大鼠的疼痛行为?

Does single cortical spreading depression elicit pain behaviour in freely moving rats?

机构信息

Gazi University Faculty of Medicine, Neuropsychiatry Centre, Ankara, Turkey.

出版信息

Cephalalgia. 2010 Oct;30(10):1195-206. doi: 10.1177/0333102409360828. Epub 2010 Mar 31.

Abstract

INTRODUCTION

Behavioural animal studies are critical, particularly to translate results to human beings. Cortical spreading depression (CSD) has been implicated in migraine pathogenesis. We aimed to investigate the effects of CSD on the behaviour of freely moving rats, since available CSD models do not include awake animals.

MATERIALS AND METHODS

We developed a new model to induce single CSD by applying topical N-methyl-D-aspartate (NMDA) and employed a combination of an automated behavioural analysis system, video camera and ultrasonic vocalisation (USV) calls for the first time. Electrocorticograms were also studied during CSD in freely moving rats. Behaviour associated with cephalic pain was assessed in a group of rats that received sumatriptan. Cortical c-fos immunoreactivity was performed in order to confirm CSD.

RESULTS

NMDA induced single CSD in ipsilateral cortex, evoked freezing behaviour (P < 0.01) and increased the number of wet dog shakes (WDS; P < 0.01). Grooming, locomotion, eating, drinking, and circling were not significantly altered among groups. Ultrasonic vocalisations compatible with pain calls (22-27 kHz) were only detected in 3 out of 25 rats. Sumatriptan did not significantly reduce the freezing behaviour. CSD induced significant c-fos expression in ipsilateral cerebral cortex and amygdala (P < 0.01).

CONCLUSIONS

CSD induces freezing behaviour by invoking anxiety/fear via amygdala activation in freely-moving rats. Single CSD is unlikely to lead to severe pain in freely-moving rats, though the development of mild or vague pain cannot be excluded. The relevance of rat behavioural responses triggered by CSD to migraine symptoms in humans needs further evaluation.

摘要

简介

行为动物研究至关重要,特别是将研究结果转化为人类研究。皮质扩散性抑制(CSD)与偏头痛发病机制有关。我们旨在研究 CSD 对自由活动大鼠行为的影响,因为现有的 CSD 模型不包括清醒动物。

材料和方法

我们开发了一种新的模型,通过应用局部 N-甲基-D-天冬氨酸(NMDA)来诱导单次 CSD,并首次使用自动化行为分析系统、摄像机和超声发声(USV)呼叫相结合。还在自由活动大鼠中研究了 CSD 期间的脑电图。在接受舒马曲坦的一组大鼠中评估了与头部疼痛相关的行为。进行皮质 c-fos 免疫反应以确认 CSD。

结果

NMDA 在同侧皮质诱导单次 CSD,引起冻结行为(P < 0.01)并增加湿狗抖动(WDS;P < 0.01)的数量。在各组之间,梳理、运动、进食、饮水和盘旋没有明显改变。只有 25 只大鼠中的 3 只检测到与疼痛呼叫(22-27 kHz)兼容的超声发声。舒马曲坦不能显著减少冻结行为。CSD 在同侧大脑皮层和杏仁核中诱导显著的 c-fos 表达(P < 0.01)。

结论

CSD 通过激活杏仁核引起焦虑/恐惧,在自由活动的大鼠中引起冻结行为。单次 CSD 不太可能导致自由活动的大鼠产生严重疼痛,但不能排除轻度或模糊疼痛的发生。CSD 引发的大鼠行为反应与偏头痛症状在人类中的相关性需要进一步评估。

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