• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

Selective vulnerability of spinal cord motor neurons to non-NMDA toxicity.

作者信息

Saroff D, Delfs J, Kuznetsov D, Geula C

机构信息

Department of Medicine (Neuroscience), Harvard Medical School, Boston, MA, USA.

出版信息

Neuroreport. 2000 Apr 7;11(5):1117-21. doi: 10.1097/00001756-200004070-00041.

DOI:10.1097/00001756-200004070-00041
PMID:10790892
Abstract

We previously reported that alpha-motor neurons in organotypic cultures of rat spinal cord (OTC-SC) are resistant to excitotoxicity induced through NMDA receptors. Here we describe the effects of non-NMDA glutamate receptor agonists kainic acid (KA) and quisqualic acid (QUIS) on motor neurons in OTC-SC. Large ventral horn acetylcholinesterase-positive neurons (VHANs), most of which are motor neurons, were quite sensitive to QUIS and KA toxicity and displayed losses of 95% and 94%, respectively. Small VHANs were reduced by 41% and 61% only. Identical results were obtained in cultures stained for non-phosphorylated neurofilaments. These observations demonstrate that alpha-motor neurons are considerably more sensitive to KA and QUIS than to NMDA toxicity. The proposed excitotoxic mechanism of ALS, therefore, is most likely mediated through non-NMDA glutamate receptors.

摘要

相似文献

1
Selective vulnerability of spinal cord motor neurons to non-NMDA toxicity.
Neuroreport. 2000 Apr 7;11(5):1117-21. doi: 10.1097/00001756-200004070-00041.
2
Slow and selective death of spinal motor neurons in vivo by intrathecal infusion of kainic acid: implications for AMPA receptor-mediated excitotoxicity in ALS.通过鞘内注射海藻酸在体内诱导脊髓运动神经元缓慢且选择性死亡:对肌萎缩侧索硬化症中AMPA受体介导的兴奋性毒性的启示
J Neurochem. 2006 Aug;98(3):782-91. doi: 10.1111/j.1471-4159.2006.03903.x.
3
Excitotoxicity mediated by non-NMDA receptors causes distal axonopathy in long-term cultured spinal motor neurons.由非NMDA受体介导的兴奋毒性在长期培养的脊髓运动神经元中导致远端轴突病。
Eur J Neurosci. 2007 Oct;26(8):2151-9. doi: 10.1111/j.1460-9568.2007.05845.x. Epub 2007 Oct 1.
4
Excitotoxic motoneuron degeneration induced by glutamate receptor agonists and mitochondrial toxins in organotypic cultures of chick embryo spinal cord.谷氨酸受体激动剂和线粒体毒素在鸡胚脊髓器官型培养物中诱导的兴奋性毒性运动神经元变性。
J Comp Neurol. 2009 Oct 1;516(4):277-90. doi: 10.1002/cne.22118.
5
Excitotoxicity in the embryonic chick spinal cord.胚胎期鸡脊髓中的兴奋毒性
Ann Neurol. 1991 Dec;30(6):758-66. doi: 10.1002/ana.410300604.
6
Glutamatergic receptors regulate expression, phosphorylation and accumulation of neurofilaments in spinal cord neurons.谷氨酸能受体调节脊髓神经元中神经丝的表达、磷酸化和积累。
Neuroscience. 1999;93(3):1123-33. doi: 10.1016/s0306-4522(99)00200-6.
7
N-methyl-D-aspartate receptor-mediated mitochondrial Ca(2+) overload in acute excitotoxic motor neuron death: a mechanism distinct from chronic neurotoxicity after Ca(2+) influx.N-甲基-D-天冬氨酸受体介导的线粒体Ca(2+)超载在急性兴奋性毒性运动神经元死亡中的作用:一种不同于Ca(2+)内流后慢性神经毒性的机制。
J Neurosci Res. 2001 Mar 1;63(5):377-87. doi: 10.1002/1097-4547(20010301)63:5<377::AID-JNR1032>3.0.CO;2-#.
8
Differential cortico-motoneuron vulnerability after chronic mitochondrial inhibition in vitro and the role of glutamate receptors.体外慢性线粒体抑制后皮质运动神经元的差异性易损性及谷氨酸受体的作用
Brain Res. 2001 Dec 20;922(2):243-9. doi: 10.1016/s0006-8993(01)03178-x.
9
Protective effect of parvalbumin on excitotoxic motor neuron death.小清蛋白对兴奋性毒性运动神经元死亡的保护作用。
Exp Neurol. 2002 Apr;174(2):150-61. doi: 10.1006/exnr.2001.7858.
10
Early signs of motoneuron vulnerability in a disease model system: Characterization of transverse slice cultures of spinal cord isolated from embryonic ALS mice.疾病模型系统中运动神经元易损性的早期迹象:从胚胎性肌萎缩侧索硬化症(ALS)小鼠分离的脊髓横切片培养物的特征分析
Neuroscience. 2006;138(4):1179-94. doi: 10.1016/j.neuroscience.2005.12.009. Epub 2006 Jan 25.

引用本文的文献

1
Acute Cellular and Functional Changes With a Combinatorial Treatment of Ion Channel Inhibitors Following Spinal Cord Injury.脊髓损伤后离子通道抑制剂联合治疗引起的急性细胞和功能变化
Front Mol Neurosci. 2020 Jun 25;13:85. doi: 10.3389/fnmol.2020.00085. eCollection 2020.
2
Glutamate transporters and the excitotoxic path to motor neuron degeneration in amyotrophic lateral sclerosis.谷氨酸转运体与肌萎缩侧索硬化症运动神经元变性的兴奋性毒性途径。
Antioxid Redox Signal. 2009 Jul;11(7):1587-602. doi: 10.1089/ars.2009.2444.
3
Glutamate carboxypeptidase II inhibition protects motor neurons from death in familial amyotrophic lateral sclerosis models.
谷氨酸羧肽酶II抑制可保护家族性肌萎缩侧索硬化模型中的运动神经元免于死亡。
Proc Natl Acad Sci U S A. 2003 Aug 5;100(16):9554-9. doi: 10.1073/pnas.1530168100. Epub 2003 Jul 22.
4
Excitotoxic and excitoprotective mechanisms: abundant targets for the prevention and treatment of neurodegenerative disorders.兴奋性毒性和兴奋性保护机制:预防和治疗神经退行性疾病的丰富靶点。
Neuromolecular Med. 2003;3(2):65-94. doi: 10.1385/NMM:3:2:65.