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T-588通过丝裂原活化蛋白激酶信号通路抑制星形胶质细胞凋亡。

T-588 inhibits astrocyte apoptosis via mitogen-activated protein kinase signal pathway.

作者信息

Takuma K, Fujita T, Kimura Y, Tanabe M, Yamamuro A, Lee E, Mori K, Koyama Y, Baba A, Matsuda T

机构信息

Department of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Kobe Gakuin University, 518 Arise, Ikawadani-cho, Nishi-ku, 651-2180, Kobe, Japan.

出版信息

Eur J Pharmacol. 2000 Jun 30;399(1):1-8. doi: 10.1016/s0014-2999(00)00334-4.

Abstract

The effect of (1R)-1-benzo[b]thiophen-5-yl-2-[2-(diethylamino)ethoxy]ethan -1-ol hydrochloride (T-588), a cognition enhancer, on reperfusion injury was studied in cultured rat astrocytes. T-588 at 1-10 microM partially protected astrocytes against reperfusion injury after exposure to Ca(2+)-free medium or hydrogen peroxide. Nerve growth factor (NGF) had a similar protective effect. Addition of both T-588 and NGF resulted in complete protection against Ca(2+) reperfusion injury. T-588 did not stimulate NGF production in astrocytes. The effect of T-588 on Ca(2+) reperfusion injury including apoptosis was inhibited by the mitogen-activated protein (MAP)/extracellular signal-regulated kinase (ERK) kinase inhibitor 2'-amino-3'-methoxyflavone (PD98059), but not by the phosphoinositide 3-kinase inhibitor wortmannin. The effect of NGF was inhibited by PD98059 and wortmannin. T-588 stimulated rapidly the phosphorylation of ERK, but did not affect that of Akt in astrocytes. These findings suggest that the ERK MAP kinase pathway has a role in the protective effects of T-588 and NGF.

摘要

认知增强剂(1R)-1-苯并[b]噻吩-5-基-2-[2-(二乙氨基)乙氧基]乙醇盐酸盐(T-588)对培养的大鼠星形胶质细胞再灌注损伤的影响进行了研究。1-10 microM的T-588可部分保护星形胶质细胞免受无钙培养基或过氧化氢暴露后的再灌注损伤。神经生长因子(NGF)具有类似的保护作用。同时添加T-588和NGF可完全保护细胞免受钙离子再灌注损伤。T-588不会刺激星形胶质细胞产生NGF。促分裂原活化蛋白(MAP)/细胞外信号调节激酶(ERK)激酶抑制剂2'-氨基-3'-甲氧基黄酮(PD98059)可抑制T-588对包括凋亡在内的钙离子再灌注损伤的作用,但磷脂酰肌醇3-激酶抑制剂渥曼青霉素则无此作用。PD98059和渥曼青霉素均可抑制NGF的作用。T-588可迅速刺激星形胶质细胞中ERK的磷酸化,但不影响Akt的磷酸化。这些发现表明,ERK MAP激酶途径在T-588和NGF的保护作用中发挥作用。

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