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在大鼠脑池内给予丝裂原活化蛋白激酶抑制剂可减轻白细胞介素-1β诱导的大鼠口面部镜像机械性痛觉过敏。

Intracisternal administration of mitogen-activated protein kinase inhibitors reduced IL-1beta-induced mirror-image mechanical allodynia in the orofacial area of rats.

作者信息

Yang Chang Sik, Jung Chang Young, Ju Jin Sook, Lee Min Kyung, Ahn Dong Kuk

机构信息

Department of Oral Physiology and Neurobiology, School of Dentistry, Kyungpook National University, 188-1 Sam Deok 2ga, Chung-gu, Daegu 700-412, Korea.

出版信息

Neurosci Lett. 2005 Oct 14;387(1):32-7. doi: 10.1016/j.neulet.2005.07.019.

Abstract

The present study investigated the role of central mitogen-activated protein kinases (MAPKs) in interleukin-1beta (IL-1beta)-induced mirror-image mechanical allodynia in the orofacial area. Experiments were carried out on Sprague-Dawley rats. Under pentobarbital sodium anesthesia, a polyethylene tube was implanted in the subcutaneous area of one vibrissa pad, which enabled us to inject IL-1beta. For an intracisternal injection, each anesthetized rat was mounted on a stereotaxic frame and a polyethylene tube was implanted. Animals were given a recovery time of at least 72 h from surgery. After a subcutaneous administration of 0.01, 0.1, 1, or 10 pg of IL-1beta, we examined the face withdrawal behavioral responses produced by 10 successive trials of air puffs ipsilateral or contralateral to the IL-1beta injection site. Normal animals did not respond to pressure less than 40 psi. The thresholds of air puffs ipsilateral and contralateral to the IL-1beta injection site were significantly lower in the IL-1beta-treated group, compared with the vehicle-treated group. The decrease in the threshold of air puffs appeared 10 min after an IL-1beta injection and persisted for over 3h. Intracisternal pretreatment with PD98059, a p44/42 MAPK inhibitor, or SB203580, a p38 MAPK inhibitor, significantly reduced the decrease in the threshold of air puffs ipsilateral to the IL-1beta injection site produced by 10 pg of IL-1beta. IL-1beta-induced mirror-image mechanical allodynia was also reduced significantly by intracisternal pretreatment with both PD98059 and SB203580. These results indicate that central MAPK pathways mediate IL-1beta-induced mirror-image mechanical allodynia in the orofacial area.

摘要

本研究调查了中枢丝裂原活化蛋白激酶(MAPK)在白细胞介素-1β(IL-1β)诱导的口面部镜像机械性异常性疼痛中的作用。实验在Sprague-Dawley大鼠身上进行。在戊巴比妥钠麻醉下,将一根聚乙烯管植入一侧触须垫的皮下区域,以便我们注射IL-1β。进行脑池内注射时,将每只麻醉的大鼠固定在立体定位框架上并植入一根聚乙烯管。动物术后至少恢复72小时。皮下注射0.01、0.1、1或10 pg的IL-1β后,我们检查了在IL-1β注射部位同侧或对侧连续10次吹气所产生的面部退缩行为反应。正常动物对小于40 psi的压力无反应。与溶剂处理组相比,IL-1β处理组中IL-1β注射部位同侧和对侧的吹气阈值显著降低。吹气阈值的降低在IL-1β注射后10分钟出现,并持续超过3小时。用p44/42 MAPK抑制剂PD98059或p38 MAPK抑制剂SB203580进行脑池内预处理,可显著降低10 pg IL-1β所引起的IL-1β注射部位同侧吹气阈值的降低。用PD98059和SB203580进行脑池内预处理也可显著减轻IL-1β诱导的镜像机械性异常性疼痛。这些结果表明,中枢MAPK通路介导了IL-1β诱导的口面部镜像机械性异常性疼痛。

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