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一氧化氮和超氧化物促成了因营养因子剥夺所诱导的运动神经元凋亡。

Nitric oxide and superoxide contribute to motor neuron apoptosis induced by trophic factor deprivation.

作者信息

Estévez A G, Spear N, Manuel S M, Radi R, Henderson C E, Barbeito L, Beckman J S

机构信息

Department of Anesthesiology, The University of Alabama at Birmingham, Birmingham, Alabama 35233, USA.

出版信息

J Neurosci. 1998 Feb 1;18(3):923-31. doi: 10.1523/JNEUROSCI.18-03-00923.1998.

Abstract

Primary cultures of rat embryonic motor neurons deprived of brain-derived neurotrophic factor (BDNF) induce neuronal nitric oxide synthase (NOS) within 18 hr. Subsequently, >60% of the neurons undergo apoptosis between 18 and 24 hr after plating. Nitro-L-arginine and nitro-L-arginine methyl ester (L-NAME) prevented motor neuron death induced by trophic factor deprivation. Exogenous generation of nitric oxide at concentrations lower than 100 nM overcame the protection by L-NAME. Manganese tetrakis (4-benzoyl acid) porphyrin, a cell-permeant superoxide scavenger, also prevented nitric oxide-dependent motor neuron death. Motor neurons cultured without trophic support rapidly became immunoreactive for nitrotyrosine when compared with motor neurons incubated with BDNF, L-NAME, or manganese TBAP. Our results suggest that peroxynitrite, a strong oxidant formed by the reaction of NO and superoxide, plays an important role in the induction of apoptosis in motor neurons deprived of trophic factors and that BDNF supports motor neuron survival in part by preventing neuronal NOS expression.

摘要

去除脑源性神经营养因子(BDNF)的大鼠胚胎运动神经元原代培养物在18小时内诱导神经元型一氧化氮合酶(NOS)。随后,接种后18至24小时内超过60%的神经元发生凋亡。硝基-L-精氨酸和硝基-L-精氨酸甲酯(L-NAME)可防止营养因子剥夺诱导的运动神经元死亡。浓度低于100 nM的一氧化氮外源性生成可克服L-NAME的保护作用。锰四(4-苯甲酸)卟啉,一种可穿透细胞的超氧化物清除剂,也可防止一氧化氮依赖性运动神经元死亡。与用BDNF、L-NAME或锰四(4-苯甲酸)卟啉(锰TBAP)孵育的运动神经元相比,在没有营养支持的情况下培养的运动神经元迅速对硝基酪氨酸产生免疫反应。我们的结果表明,过氧亚硝酸盐,一种由一氧化氮和超氧化物反应形成的强氧化剂,在营养因子剥夺的运动神经元凋亡诱导中起重要作用,并且BDNF部分通过防止神经元型NOS表达来支持运动神经元存活。

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