Endothelin-1 inhibition of the ATP-Sensitive K+ channel in guinea-pig ventricular cardiomyocytes

被引:9
|
作者
Satoh, H
机构
[1] Department of Pharmacology, Nara Medical University, Kashihara, Nara 634, Japan
来源
GENERAL PHARMACOLOGY | 1995年 / 26卷 / 07期
关键词
endothelin-1; ATP-sensitive K+ channel; glibenclamide; cell-attached voltage-clamp; patch-clamp experiments;
D O I
10.1016/0306-3623(95)00046-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. Effects of endothelin-1, on the ATP-sensitive K+ channel were examined in guinea-pig ventricular cardiomyocytes. 2. The ATP-sensitive K+ channel was activated outwardly with amplitude of about 2.2 pA at 0 mV. The conductance was 31 pS at 5.4 mM external K+ solution. The open probability was inhibited, and was completely blocked at 1 nM of endothelin-1. 3. In contrast, endothelin-3 (1 nM) did not cause any effects on the channels. 4. Endothelin-1 (10 nM) significantly prolonged the action potential duration. These responses were reversible. 5. These results suggest that endothelin-1 may reverse the physiological responses to the stimulation of ATP-sensitive K+ channels, indicating its regulatory mechanisms under the disease conditions.
引用
收藏
页码:1549 / 1552
页数:4
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