Suppr超能文献

症状前肌萎缩侧索硬化症小鼠培养的脊髓运动神经元的兴奋性过高

Hyperexcitability of cultured spinal motoneurons from presymptomatic ALS mice.

作者信息

Kuo Jason J, Schonewille Martijn, Siddique Teepu, Schults Annet N A, Fu Ronggen, Bär Peter R, Anelli Roberta, Heckman C J, Kroese Alfons B A

机构信息

Department of Physiology, Northwestern University Medical School, Chicago, Illinois 60611, USA.

出版信息

J Neurophysiol. 2004 Jan;91(1):571-5. doi: 10.1152/jn.00665.2003. Epub 2003 Oct 1.

Abstract

ALS (amyotrophic lateral sclerosis) is an adult-onset and deadly neurodegenerative disease characterized by a progressive and selective loss of motoneurons. Transgenic mice overexpressing a mutated human gene (G93A) coding for the enzyme SOD1 (Cu/Zn superoxide dismutase) develop a motoneuron disease resembling ALS in humans. In this generally accepted ALS model, we tested the electrophysiological properties of individual embryonic and neonatal spinal motoneurons in culture by measuring a wide range of electrical properties influencing motoneuron excitability during current clamp. There were no differences in the motoneuron resting potential, input conductance, action potential shape, or afterhyperpolarization between G93A and control motoneurons. The relationship between the motoneuron's firing frequency and injected current (f-I relation) was altered. The slope of the f-I relation and the maximal firing rate of the G93A motoneurons were much greater than in the control motoneurons. Differences in spontaneous synaptic input were excluded as a cause of increased excitability. This finding identifies a markedly elevated intrinsic electrical excitability in cultured embryonic and neonatal mutant G93A spinal motoneurons. We conclude that the observed intrinsic motoneuron hyperexcitability is induced by the SOD1 toxic gain-of-function through an aberration in the process of action potential generation. This hyperexcitability may play a crucial role in the pathogenesis of ALS as the motoneurons were cultured from presymptomatic mice.

摘要

肌萎缩侧索硬化症(ALS)是一种成年发病的致命性神经退行性疾病,其特征为运动神经元进行性、选择性丧失。过表达编码超氧化物歧化酶1(Cu/Zn超氧化物歧化酶)的突变人类基因(G93A)的转基因小鼠会患上一种类似于人类ALS的运动神经元疾病。在这个被广泛接受的ALS模型中,我们通过测量电流钳制期间影响运动神经元兴奋性的多种电学特性,测试了培养的单个胚胎和新生脊髓运动神经元的电生理特性。G93A运动神经元和对照运动神经元在静息电位、输入电导、动作电位形状或超极化后电位方面没有差异。运动神经元的放电频率与注入电流之间的关系(f-I关系)发生了改变。G93A运动神经元的f-I关系斜率和最大放电率比对照运动神经元大得多。自发突触输入的差异被排除为兴奋性增加的原因。这一发现表明培养的胚胎和新生突变G93A脊髓运动神经元的内在电兴奋性明显升高。我们得出结论,观察到的运动神经元内在兴奋性过高是由SOD1功能获得性毒性通过动作电位产生过程中的异常诱导的。由于运动神经元是从症状前小鼠培养而来的,这种兴奋性过高可能在ALS的发病机制中起关键作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验