Cyclic GMP generation mediated by 5-HT-2 receptors via nitric oxide-dependent pathway and its effect on the desensitization of 5-HT-2 receptors in C6 glioma cells.

A Kagaya, N Motohashi, A Kugaya, T Yamaji, T Hayashi, Y Okamoto, H Shinno, M Takebayashi, Y Uchitomi, S Yamawaki
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引用次数: 4

Abstract

Serotonin (5-HT)-2 receptor-mediated cGMP generation was investigated in comparison with calcium (Ca2+) mobilization in C6 glioma cells. 5-HT enhanced cGMP generation, and risperidone and ketanserin potently blocked the response. These results indicate that 5-HT-2 receptors are responsible for the cGMP generation. 5-HT-induced cGMP production was completely abolished by BAPTA, an intracellular Ca2+ chelating agent, or NG-mono-methyl-L-arginine(NMMA), a nitric oxide synthase (NOS) inhibitor, suggesting that 5-HT-induced cGMP generation was through nitric oxide (NO)-dependent pathway. 5-HT (10 microM)-elicited Ca2+ mobilization and cGMP generation were reduced to 40 and 15% after pretreatment with 10 microM 5-HT for 4 hours. NMMA did not modify 5-HT-induced desensitization of either Ca2+ mobilization or cGMP generation, suggesting that NO pathway is independent of the desensitization. The present study has demonstrated the nature of 5-HT-2 receptor-mediated cGMP generation in C6 glioma cells.

一氧化氮依赖途径5-HT-2受体介导C6胶质瘤细胞产生环状GMP及其对5-HT-2受体脱敏的影响
研究了C6胶质瘤细胞中5-羟色胺(5-HT)-2受体介导的cGMP生成与钙(Ca2+)动员的比较。5-羟色胺增强cGMP的产生,利培酮和酮色林有效地阻断了这一反应。这些结果表明5-HT-2受体参与了cGMP的产生。5- ht诱导的cGMP产生被细胞内Ca2+螯合剂BAPTA或一氧化氮合酶(NOS)抑制剂NG-mono-methyl-L-arginine(NMMA)完全消除,表明5- ht诱导的cGMP产生是通过一氧化氮(NO)依赖途径产生的。10微米5-HT预处理4小时后,5-HT(10微米)诱导的Ca2+动员和cGMP生成分别减少到40%和15%。NMMA没有改变5- ht诱导的Ca2+动员或cGMP产生的脱敏,表明NO途径独立于脱敏。本研究证实了C6胶质瘤细胞中5-HT-2受体介导的cGMP生成的性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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