Suppr超能文献

N-甲基-D-天冬氨酸受体拮抗作用对VX诱导的培养大鼠皮层神经元细胞死亡的保护作用。

Protective effects of N-methyl-D-aspartate receptor antagonism on VX-induced neuronal cell death in cultured rat cortical neurons.

作者信息

Wang Yushan, Weiss M Tracy, Yin Junfei, Tenn Catherine C, Nelson Peggy D, Mikler John R

机构信息

Canada West Bioscience Inc., Camrose, Alberta, Canada.

出版信息

Neurotox Res. 2008 May-Jun;13(3-4):163-72. doi: 10.1007/BF03033500.

Abstract

Exposure of the central nervous system to organophosphorus (OP) nerve agents induces seizures and neuronal cell death. Here we report that the OP nerve agent, VX, induces apoptotic-like cell death in cultured rat cortical neurons. The VX effects on neurons were concentration-dependent, with an IC(50) of approximately 30 microM. Blockade of N-methyl-D-aspartate receptors (NMDAR) with 50 microM. D-2-amino-5-phosphonovalerate (APV) diminished 30 microM VX-induced total cell death, as assessed by alamarBlue assay and Hoechst staining. In contrast, neither antagonists of alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptors (AMPARs) nor metabotropic glutamate receptors (mGluRs) had any effect on VX-induced neurotoxicity. VX-induced neuronal cell death could not be solely attributed to acetylcholinesterase (AChE) inhibition, since neither the reversible pharmacological cholinesterase inhibitor, physostigmine, nor the muscarinic receptor antagonist, atropine, affected VX-induced cell death. Importantly, APV was found to be therapeutically effective against VX-induced cell death up to 2 h post VX exposure. These results suggest that NMDARs, but not AMPARs or mGluRs, play important roles in VX-induced cell death in cultured rat cortical neurons. Based on their therapeutic effects, NMDAR antagonists may be beneficial in the treatment of VX-induced neurotoxicities.

摘要

中枢神经系统暴露于有机磷(OP)神经毒剂会引发癫痫发作和神经元细胞死亡。在此我们报告,OP神经毒剂VX可在培养的大鼠皮质神经元中诱导凋亡样细胞死亡。VX对神经元的作用呈浓度依赖性,半数抑制浓度(IC50)约为30微摩尔。用50微摩尔D-2-氨基-5-磷酸戊酸(APV)阻断N-甲基-D-天冬氨酸受体(NMDAR),可减少30微摩尔VX诱导的总细胞死亡,这通过alamarBlue检测法和Hoechst染色评估得出。相比之下,α-氨基-3-羟基-5-甲基异恶唑-4-丙酸受体(AMPAR)拮抗剂和代谢型谷氨酸受体(mGluR)拮抗剂对VX诱导的神经毒性均无任何影响。VX诱导的神经元细胞死亡不能单纯归因于乙酰胆碱酯酶(AChE)抑制,因为可逆性药理胆碱酯酶抑制剂毒扁豆碱和毒蕈碱受体拮抗剂阿托品均未影响VX诱导的细胞死亡。重要的是,发现APV在VX暴露后长达2小时内对VX诱导的细胞死亡具有治疗效果。这些结果表明,NMDAR而非AMPAR或mGluR在VX诱导的培养大鼠皮质神经元细胞死亡中起重要作用。基于其治疗效果,NMDAR拮抗剂可能对治疗VX诱导的神经毒性有益。

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