题名 | 2-BFI attenuates experimental autoimmune encephalomyelitis-induced spinal cord injury with enhanced B-CK, CaATPase, but reduced calpain activity |
作者 | |
发表日期 | 2011-03-04 |
发表期刊 | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | 2-BFI Brain-creatine kinase CaATPase Calpain Imidazoline 2 receptor Experimental autoimmune encephalomyelitis Multiple sclerosis |
其他关键词 | ISCHEMIC MOUSE-BRAIN ; MULTIPLE-SCLEROSIS ; CEREBRAL-ISCHEMIA ; GLUTAMATE TOXICITY ; NEURONAL DEATH ; EXPRESSION ; NEURODEGENERATION ; DEMYELINATION ; INFLAMMATION ; MECHANISMS |
摘要 | The lack of disease-modifying pharmacological agents for effective treatment of multiple sclerosis (MS) still represents a large and urgent unmet medical need. Our previous studies showed that ligands to type 2 imidazoline receptors (I2R) were effective in protecting spinal cord injury caused by experimental autoimmune encephalomyelitis (EAE), a mouse model of MS. In this study, we further examined the protective property of a very selective ligand of I2R, 2-(2-benzofuranyl) 2-imidazoline (2-BFI) against EAE. Importantly, a mechanism of 2-BFI-mediated protection was investigated which possibly involves an I2R binding protein, brain-creatine kinase (B-CK), as well as CaATPase and calpain. The enzymatic activity of B-CK and CaATPase was significantly reduced in EAE injured spinal cord. Reduction of B-CK activity in EAE spinal cord may lead to energy reduction and dysfunction in cellular calcium homeostasis. Increased intracellular calcium evokes elevation of calpain activity occurring in EAE spinal cord which causes further tissue damage. Indeed, EAE injured spinal cord showed significant reduction in CaATPase and increase calpain activities. Remarkably, spinal cord tissue from mice treated daily with 2-BFI during the progression of EAE significantly restored B-CK and CaATPase enzymatic activities and showed no induction in calpain activity. Moreover, EAE spinal cord from 2-BFI treated mice also demonstrated better preservation of myelin; reduced axonal injury, as evidenced by the lower level of beta-APP expression, and above all, highly improved neurobehavioral scores (p < 0.01; n = 10). These findings suggest that 2-BFI can be further developed as a therapeutic drug for MS treatment. Crown Copyright (C) 2011 Published by Elsevier Inc. All rights reserved. |
资助项目 | Chinese National Natural Science FoundationNational Natural Science Foundation of China (NSFC) [81070960]; Zhejiang Provincial Natural Science [Y207494]; Zhejiang Key Subject (Pharmacology and Biochemical Pharmaceutics); 3010 grant |
出版者 | ACADEMIC PRESS INC ELSEVIER SCIENCE |
出版地 | SAN DIEGO |
ISSN | 0006-291X |
EISSN | 1090-2104 |
卷号 | 406期号:1页码:152-157 |
DOI | 10.1016/j.bbrc.2011.02.018 |
页数 | 6 |
WOS类目 | Biochemistry & Molecular Biology ; Biophysics |
WOS研究方向 | Biochemistry & Molecular Biology ; Biophysics |
WOS记录号 | WOS:000288302100028 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 21303658 |
SCOPUSEID | 2-s2.0-79952185502 |
通讯作者地址 | [Zheng, Rong-Yuan]First Affiliated Hosp, Dept Neurol, 2 Fuxue Lane, Wenzhou City 325000, Zhejiang, Peoples R China. |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/5358 |
专题 | 药学院(分析测试中心)_实验神经生物研究所 |
通讯作者 | Zheng, Rong-Yuan |
作者单位 | 1.First Affiliated Hosp, Dept Neurol, Wenzhou City 325000, Zhejiang, Peoples R China; 2.Wenzhou Med Coll, Res Inst Expt Neurobiol, Wenzhou City 325000, Zhejiang, Peoples R China; 3.Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada |
第一作者单位 | 药学院(分析测试中心)_实验神经生物研究所 |
推荐引用方式 GB/T 7714 | Wang, Pei,Wang, Zhao-Wei,Lin, Fu-Hong,et al. 2-BFI attenuates experimental autoimmune encephalomyelitis-induced spinal cord injury with enhanced B-CK, CaATPase, but reduced calpain activity[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2011,406(1):152-157. |
APA | Wang, Pei, Wang, Zhao-Wei, Lin, Fu-Hong, Han, Zhao, Hou, Sheng-Tao, & Zheng, Rong-Yuan. (2011). 2-BFI attenuates experimental autoimmune encephalomyelitis-induced spinal cord injury with enhanced B-CK, CaATPase, but reduced calpain activity. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 406(1), 152-157. |
MLA | Wang, Pei,et al."2-BFI attenuates experimental autoimmune encephalomyelitis-induced spinal cord injury with enhanced B-CK, CaATPase, but reduced calpain activity".BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 406.1(2011):152-157. |
条目包含的文件 | 条目无相关文件。 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论