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[神经营养因子对皮层培养物中谷氨酸神经毒性的保护作用]

[Protective effect of neurotrophin against glutamate neurotoxicity in cortical cultures].

作者信息

Kume T, Katsuki H, Kaneko S, Akaike A

机构信息

Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto University, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1998 Oct;112 Suppl 1:98P-102P. doi: 10.1254/fpj.112.supplement_98.

Abstract

This study was performed to investigate the effects of neurotrophins on glutamate cytotoxicity by using cultured cortical neurons. Primary cultures obtained from the cerebral cortex of fetal rats (17-19 days gestation) were used for experiments. NGF did not elicit tyrosine phosphorylation of Trks whereas BDNF induced Trk tyrosine phosphorylation within 10 min, followed by time-dependent decrease. Brief glutamate exposure to the cell induced delayed cytotoxicity. Similar cytotoxicity was observed with the brief application of a calcium ionophore, ionomycin, and nitric oxide (NO) generating agents, S-nitrosocysteine (SNOC) and SIN-1. Exposure of the cultures to NGF and BDNF for 1 or 24 hr prior to glutamate exposure reduced glutamate-induced cytotoxicity. In contrast, simultaneous addition of NGF and BDNF with glutamate did not affect glutamate-induced cytotoxicity. Ionomycin-induced cytotoxicity was prevented by exposing cultures to NGF and BDNF for 24-hr. Moreover, NGF and BDNF ameliorated cytotoxicity induced by SNOC and SIN-1. These results suggest that neurotrophins prevent NO mediated glutamate cytotoxicity.

摘要

本研究旨在通过使用培养的皮质神经元来研究神经营养因子对谷氨酸细胞毒性的影响。从胎鼠(妊娠17 - 19天)大脑皮质获得的原代培养物用于实验。神经生长因子(NGF)未引发酪氨酸激酶受体(Trks)的酪氨酸磷酸化,而脑源性神经营养因子(BDNF)在10分钟内诱导Trk酪氨酸磷酸化,随后呈时间依赖性下降。短暂暴露于谷氨酸会诱导细胞延迟性细胞毒性。短暂应用钙离子载体离子霉素和一氧化氮(NO)生成剂S - 亚硝基半胱氨酸(SNOC)和SIN - 1也观察到类似的细胞毒性。在谷氨酸暴露前1或24小时将培养物暴露于NGF和BDNF可降低谷氨酸诱导的细胞毒性。相反,将NGF和BDNF与谷氨酸同时添加并不影响谷氨酸诱导的细胞毒性。通过将培养物暴露于NGF和BDNF 24小时可预防离子霉素诱导的细胞毒性。此外,NGF和BDNF可改善由SNOC和SIN - 1诱导的细胞毒性。这些结果表明神经营养因子可预防NO介导的谷氨酸细胞毒性。

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