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格列本脲特异性阻断豚鼠心脏心房肌细胞中的ATP敏感性钾通道电流。

Glibenclamide specifically blocks ATP-sensitive K+ channel current in atrial myocytes of guinea pig heart.

作者信息

Hamada E, Takikawa R, Ito H, Iguchi M, Terano A, Sugimoto T, Kurachi Y

机构信息

Second Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.

出版信息

Jpn J Pharmacol. 1990 Dec;54(4):473-7. doi: 10.1254/jjp.54.473.

Abstract

Effects of glibenclamide on the control membrane ionic currents, acetylcholine or adenosine-induced K+ current, and nicorandil-induced K+ current were examined in single atrial myocytes of guinea pig heart. The nystatin-whole cell clamp technique was used. Nicorandil evoked the time-independent K+ current which is probably the current through the ATP-sensitive K+ channel. Glibenclamide inhibited this current in a concentration-dependent fashion, although it had no effect on the other currents. We concluded that glibenclamide specifically inhibits the ATP-sensitive K+ channel current in cardiac myocytes.

摘要

在豚鼠心脏单个心房肌细胞中,研究了格列本脲对控制膜离子电流、乙酰胆碱或腺苷诱导的钾电流以及尼可地尔诱导的钾电流的影响。采用制霉菌素全细胞钳技术。尼可地尔诱发了与时间无关的钾电流,这可能是通过ATP敏感性钾通道的电流。格列本脲以浓度依赖性方式抑制该电流,尽管它对其他电流没有影响。我们得出结论,格列本脲特异性抑制心肌细胞中的ATP敏感性钾通道电流。

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