Suppr超能文献

蜘蛛毒素(JSTX)对体外培养海马CA1神经元的影响。

Effects of a spider toxin (JSTX) on hippocampal CA1 neurons in vitro.

作者信息

Saito M, Sahara Y, Miwa A, Shimazaki K, Nakajima T, Kawai N

机构信息

Department of Neurobiology, Tokyo Metropolitan Institute for Neurosciences, Japan.

出版信息

Brain Res. 1989 Feb 27;481(1):16-24. doi: 10.1016/0006-8993(89)90480-0.

Abstract

The effect of a toxin (JSTX) obtained from Nephila clavata (Joro spider) on the CA1 pyramidal neurons of the hippocampus was studied using slice preparations. JSTX blocked the excitatory postsynaptic potentials (EPSPs) in the pyramidal neuron evoked by Schaffer collateral stimulation but was without effect on the antidromic action potentials or on the resting conductance. Depolarization induced by ionophoretic application of glutamate was readily suppressed by JSTX but aspartate-induced depolarization was much less sensitive to the toxin. Among preferential agonists activating 3 receptor subtypes for excitatory amino acids, quisqualate responses were most effectively suppressed by JSTX. Kainate responses were similarly suppressed but in some cells higher concentration of the toxin was needed to block the responses. N-methyl-D-aspartate (NMDA) responses were the least sensitive to JSTX but they were suppressed by +/- 2-amino-5-phosphonovaleric acid (APV). Long term potentiation (LTP) once it had taken place was not completely inhibited by APV. In the presence of JSTX, however, LTP was blocked and tetanic stimuli produced only a short-lived potentiation. In Mg2+ free solution, an orthodromic stimulation evoked repetitive spike responses which were superimposed on the depolarization following the initial spike. APV suppressed the depolarization and associated spikes leaving an orthodromic response which was sensitive to JSTX. The results suggest that JSTX blocks EPSPs in CA1 pyramidal neurons which are mediated by non-NMDA type receptors.

摘要

利用脑片制备技术研究了从棒络新妇蛛(Joro蜘蛛)中获得的一种毒素(JSTX)对海马CA1锥体神经元的影响。JSTX可阻断由Schaffer侧支刺激诱发的锥体神经元兴奋性突触后电位(EPSP),但对逆向动作电位或静息电导无影响。离子电泳施加谷氨酸诱导的去极化很容易被JSTX抑制,但天冬氨酸诱导的去极化对该毒素的敏感性要低得多。在激活兴奋性氨基酸3种受体亚型的优先激动剂中,quisqualate反应被JSTX抑制得最有效。海人藻酸反应也同样被抑制,但在一些细胞中需要更高浓度的毒素才能阻断反应。N-甲基-D-天冬氨酸(NMDA)反应对JSTX最不敏感,但它们可被±2-氨基-5-磷酸戊酸(APV)抑制。一旦发生,长时程增强(LTP)不会被APV完全抑制。然而,在JSTX存在的情况下,LTP被阻断,强直刺激仅产生短暂的增强。在无镁溶液中,顺向刺激诱发重复锋电位反应,这些反应叠加在初始锋电位后的去极化上。APV抑制去极化和相关锋电位,留下对JSTX敏感的顺向反应。结果表明,JSTX阻断CA1锥体神经元中由非NMDA型受体介导EPSP。

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