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海马体中P2X7受体介导的p38丝裂原活化蛋白激酶磷酸化。

P2X7 receptor mediated phosphorylation of p38MAP kinase in the hippocampus.

作者信息

Papp Lilla, Vizi E Sylvester, Sperlágh Beáta

机构信息

Department of Pharmacology, Institute of Experimental Medicine, Hungarian Academy of Sciences, H-1450 Budapest, Hungary.

出版信息

Biochem Biophys Res Commun. 2007 Apr 6;355(2):568-74. doi: 10.1016/j.bbrc.2007.02.014. Epub 2007 Feb 9.

Abstract

This study was designed to explore the effect of P2X7 receptor (P2X7R) activation on the expression of p38 MAP kinase (p38 MAPK) enzyme in hippocampal slices of wild-type (WT) and P2X7R(-/-) mice using the Western blot technique and to clarify its role in P2X7 receptor mediated [(3)H]glutamate release. ATP (1 mM) and the P2X7R agonist BzATP (100 microM) significantly increased p38 MAPK phosphorylation in WT mice, and these effects were absent in the hippocampal slices of P2X7R(-/-) mice. Both ATP- and BzATP-induced p38 MAPK phosphorylations were sensitive to the p38 MAP kinase inhibitor, SB203580 (1 microM). ATP elicited [(3)H]glutamate release from hippocampal slices, which was significantly attenuated by SB203580 (1 microM) but not by the extracellular signal-regulated kinase (ERK1/2) inhibitor, PD098095 (10 microM). Consequently, we suggest that P2X7Rs and p38 MAPK are involved in the stimulatory effect of ATP on glutamate release in the hippocampal slices of WT mice.

摘要

本研究旨在利用蛋白质印迹技术探讨P2X7受体(P2X7R)激活对野生型(WT)和P2X7R基因敲除(P2X7R(-/-))小鼠海马切片中p38丝裂原活化蛋白激酶(p38 MAPK)表达的影响,并阐明其在P2X7受体介导的[³H]谷氨酸释放中的作用。ATP(1 mM)和P2X7R激动剂BzATP(100 μM)显著增加WT小鼠中p38 MAPK的磷酸化,而在P2X7R(-/-)小鼠的海马切片中未观察到这些效应。ATP和BzATP诱导的p38 MAPK磷酸化均对p38 MAP激酶抑制剂SB203580(1 μM)敏感。ATP可引起海马切片释放[³H]谷氨酸,SB203580(1 μM)可显著减弱这种释放,但细胞外信号调节激酶(ERK1/2)抑制剂PD098095(10 μM)则无此作用。因此,我们认为P2X7R和p38 MAPK参与了ATP对WT小鼠海马切片中谷氨酸释放的刺激作用。

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