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甘氨酸诱发大鼠纹状体切片释放[3H]乙酰胆碱与N-甲基-D-天冬氨酸受体无关。

Glycine-evoked release of [3H]acetylcholine from rat striatal slices is independent of the NMDA receptor.

作者信息

Taylor C A, Tsai C, Lehmann J

机构信息

Ciba-Geigy Corp., Pharmaceuticals Division, Summit, NJ 07901.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1988 May;337(5):552-5. doi: 10.1007/BF00182730.

Abstract

KCl-, NMDA-, and glycine-evoked release of [3H]acetylcholine was studied in superfused rat striatal slices. KCl-evoked release of [3H]acetylcholine was inhibited by 1.2 mM MgCl2 and 100 microM lidocaine. Similarly, NMDA-evoked release was inhibited by MgCl2 and lidocaine as well as 10 microM CGS 19755, a competitive antagonist at NMDA receptors, and 10 nM MK-801, a noncompetitive antagonist of NMDA-induced responses. Glycine-evoked release was calcium-dependent and was inhibited by 0.1 microM strychnine whereas KCl- and NMDA-evoked release were resistant to strychnine. In addition, lidocaine inhibited the glycine-induced response. Cross-tachyphylaxis was not observed between NMDA- and glycine-evoked release. These results indicate that the strychnine-sensitive, glycine-evoked release of [3H]acetylcholine is independent of the NMDA receptor.

摘要

在灌流的大鼠纹状体切片中研究了氯化钾、N-甲基-D-天冬氨酸(NMDA)和甘氨酸诱发的[3H]乙酰胆碱释放。1.2 mM氯化镁和100 μM利多卡因抑制了氯化钾诱发的[3H]乙酰胆碱释放。同样,NMDA诱发的释放也受到氯化镁、利多卡因以及10 μM CGS 19755(一种NMDA受体竞争性拮抗剂)和10 nM MK-801(一种NMDA诱导反应的非竞争性拮抗剂)的抑制。甘氨酸诱发的释放依赖于钙,并且受到0.1 μM士的宁的抑制,而氯化钾和NMDA诱发的释放对士的宁有抗性。此外,利多卡因抑制了甘氨酸诱导的反应。在NMDA和甘氨酸诱发的释放之间未观察到交叉快速耐受性。这些结果表明,士的宁敏感的、甘氨酸诱发的[3H]乙酰胆碱释放独立于NMDA受体。

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