综述

Nogo-A对突触可塑性的调节及相关神经疾病

  • 何梅 ,
  • 毛敏 ,
  • 赵国燕 ,
  • 汤竣杰 ,
  • 冯爽 ,
  • 鲁秀敏 ,
  • 王永堂
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  • 1. 重庆理工大学药学与生物工程学院,重庆市 400054
    2. 第三军医大学大坪医院野战外科研究所,创伤、烧伤与复合伤国家重点实验室,重庆市 400042
何梅(1991-),女,汉族,重庆市人,硕士研究生,主要研究方向:微生物与生化药学。

收稿日期: 2018-10-01

  修回日期: 2018-10-18

  网络出版日期: 2019-04-01

基金资助

1.国家自然科学基金项目(No. 81671903; No. 81772064; No. 81372040);2.重庆市研究生科研创新项目(No. CYS18313);3.重庆理工大学大学生创新训练计划项目(No. 2018CX035);4.创伤、烧伤与复合伤国家重点实验室开放基金项目(No. SKLKF201706)

Synaptic Plasticity Regulation of Nogo-A and Development of Related Neurological Diseases (review)

  • HE Mei ,
  • MAO Min ,
  • ZHAO Guo-yan ,
  • TANG Jun-jie ,
  • FENG Shuang ,
  • LU Xiu-min ,
  • WANG Yong-tang
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  • 1. College of Pharmacy and Biological Engineering, Chongqing University of Technology, Chongqing 400054, China
    2. State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, China

Received date: 2018-10-01

  Revised date: 2018-10-18

  Online published: 2019-04-01

Supported by

National Natural Science Foundation of China (No. 81671903; No. 81772064; No. 81372040),

摘要

轴突损伤往往导致成年哺乳动物中枢神经系统永久性缺损。作为轴突生长抑制剂,Nogo-A及其受体在中枢神经系统成熟神经元中参与对突触可塑性的调节作用,并与脊髓损伤、多发性硬化症、阿尔茨海默病及创伤后应激障碍等的发病有关。

本文引用格式

何梅 , 毛敏 , 赵国燕 , 汤竣杰 , 冯爽 , 鲁秀敏 , 王永堂 . Nogo-A对突触可塑性的调节及相关神经疾病[J]. 中国康复理论与实践, 2019 , 25(2) : 196 -200 . DOI: 10.3969/j.issn.1006-9771.2019.02.012

Abstract

Axonal damage leads to permanent defects in the adult mammals central nervous system. As an important axonal growth inhibitor, Nogo-A and its receptors involve in the regulation of synaptic plasticity in mature neurons of the central nervous system, and play a role in the related neurological diseases, such as spinal cord injury, multiple sclerosis, Alzheimer's disease and posttraumatic stress disorder.

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