Suppr超能文献

钙敏感受体和钙蛋白酶促成脊髓的缺血再灌注损伤。

CaSR and calpain contribute to the ischemia reperfusion injury of spinal cord.

作者信息

Sun Ji-Fu, Yang Hui-Lin, Huang Yong-Hui, Chen Qian, Cao Xing-Bing, Li Da-Peng, Shu Hao-Ming, Jiang Run-Yu

机构信息

Department of Orthopedic Surgery, The First Affiliated Hospital of Soochow University, No. 188 Shizi Street, Suzhou 215006, Jiangsu, China.

Department of Orthopedic Surgery, The First Affiliated Hospital of Soochow University, No. 188 Shizi Street, Suzhou 215006, Jiangsu, China.

出版信息

Neurosci Lett. 2017 Apr 12;646:49-55. doi: 10.1016/j.neulet.2017.03.009. Epub 2017 Mar 8.

Abstract

Spinal cord ischemia reperfusion injury (SCIRI) can cause spinal cord dysfunction and even devastating paraplegia. Calcium-sensing receptor (CaSR) and calpain are two calcium related molecules which have been reported to be involved in the ischemia reperfusion injury of cardiomyocytes and the subsequent apoptosis. Here, we studied the expression of CaSR and calpain in spinal cord neurons and tissues, followed by the further investigation of the role of CaSR/calpain axis in the cellular apoptosis process during SCIRI. The results of in vitro and in vivo studies showed that the expression of CaSR and calpain in spinal cord neurons increased during SCIRI. Moreover, the CaSR agonist GdCl and antagonist NPS-2390 enhanced or decreased the expression of CaSR and calpain respectively. The expressions of CaSR and calpain were also consistent with the cellular apoptosis in spinal cord. Taken together, CaSR-calpain contributes to the SCIRI apoptosis, and CaSR antagonist might be a helpful drug for alleviating SCIRI.

摘要

脊髓缺血再灌注损伤(SCIRI)可导致脊髓功能障碍,甚至造成严重的截瘫。钙敏感受体(CaSR)和钙蛋白酶是两种与钙相关的分子,据报道它们参与了心肌细胞的缺血再灌注损伤及随后的细胞凋亡过程。在此,我们研究了CaSR和钙蛋白酶在脊髓神经元和组织中的表达,随后进一步探讨CaSR/钙蛋白酶轴在SCIRI期间细胞凋亡过程中的作用。体外和体内研究结果表明,SCIRI期间脊髓神经元中CaSR和钙蛋白酶的表达增加。此外,CaSR激动剂GdCl和拮抗剂NPS-2390分别增强或降低了CaSR和钙蛋白酶的表达。CaSR和钙蛋白酶的表达也与脊髓中的细胞凋亡一致。综上所述,CaSR-钙蛋白酶促成了SCIRI细胞凋亡,CaSR拮抗剂可能是缓解SCIRI的一种有效药物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验