5-HT3B亚基与5-HT3A受体的共表达可降低酒精敏感性

Volodya Hayrapetyan, Monica Jenschke, Glenn H. Dillon, Tina K. Machu
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引用次数: 25

摘要

采用全细胞膜片钳电生理记录方法,研究了乙醇和三氯乙醇(TCEt)对小鼠5-羟色胺3a (5-HT3A)和5-HT3A/B受体功能的变构调节作用。乙醇增强5-HT3A受体功能,但对小鼠5-HT3A/B受体介导电流无影响。三氯乙醇(TCEt)对小鼠5-HT3A/B受体功能的增强作用远小于小鼠5-HT3A受体。当观察到酒精诱导的峰值幅度增加时,当前开始的20-80%上升阶段的斜率也增强,这表明激活率的增加可能是酒精增强5-HT3受体功能的一种机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-expression of the 5-HT3B subunit with the 5-HT3A receptor reduces alcohol sensitivity

Allosteric modulation of mouse 5-Hydroxytryptamine3A (5-HT3A) and 5-HT3A/B receptor function by ethanol and trichloroethanol (TCEt) was assessed in HEK293 cells with whole cell patch-clamp electrophysiological recordings. Ethanol enhanced 5-HT3A receptor function, but had no effect on mouse 5-HT3A/B receptor mediated currents. The enhancing action of trichloroethanol (TCEt) on mouse 5-HT3A/B receptor function was much less than that observed in the mouse 5-HT3A receptor. Where alcohol-induced increases in peak amplitude were observed, the slope of the 20–80% rising phase of current onset was also enhanced, suggesting that increases in activation rate may be one mechanism through which alcohols enhance function of the 5-HT3 receptors.

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