Yang Chang Sik, Jung Chang Young, Ju Jin Sook, Lee Min Kyung, Ahn Dong Kuk
Department of Oral Physiology and Neurobiology, School of Dentistry, Kyungpook National University, 188-1 Sam Deok 2ga, Chung-gu, Daegu 700-412, Korea.
Neurosci Lett. 2005 Oct 14;387(1):32-7. doi: 10.1016/j.neulet.2005.07.019.
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.
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。