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ATP敏感性钾通道受兔心室肌细胞内乳酸的调节。

ATP-sensitive potassium channels are modulated by intracellular lactate in rabbit ventricular myocytes.

作者信息

Han J, So I, Kim E Y, Earm Y E

机构信息

Department of Physiology and Biophysics, College of Medicine, Inje University, Korea.

出版信息

Pflugers Arch. 1993 Dec;425(5-6):546-8. doi: 10.1007/BF00374883.

Abstract

During myocardial ischemia, increased anaerobic glycolysis results in the accumulation of large amount of intracellular lactate. Effects of lactate on the ATP-sensitive potassium (KATP) channels were examined in rabbit ventricular myocytes, using the inside-out patch-clamp technique. Millimolar concentrations of lactate, applied to the cytosolic side of the patch membrane, induced openings of the KATP channel. This effect was inhibited by 0.1 mM glybenclamide. Lactate-induced openings of the channel were increased in a dose-dependent fashion. In dose-response relation for lactate, Kd (the lactate concentration producing half-maximal activation) and n (Hill coefficient) were 20 mM and 1.3, respectively (n = 5). Activation of KATP channels by lactate occurred even in the presence of 2 mM ATP. Lactate also caused a significant increase in Ki, the ATP concentration causing half-maximal inhibition, from 70 microM in control (n = 7) to 232 microM (n = 5). From the above results it could be concluded that intracellular lactate modulate KATP channels directly and such modulation may resolve the discrepancy between the low Ki in excised membrane patches and high levels of intracellular ATP concentration during myocardial ischemia or hypoxia.

摘要

在心肌缺血期间,无氧糖酵解增加导致大量细胞内乳酸堆积。采用膜片钳内面向外式技术,在兔心室肌细胞中研究了乳酸对ATP敏感性钾(KATP)通道的影响。将毫摩尔浓度的乳酸施加于膜片膜的胞质侧,可诱导KATP通道开放。这种作用被0.1 mM格列本脲抑制。乳酸诱导的通道开放呈剂量依赖性增加。对于乳酸的剂量反应关系,Kd(产生最大激活一半时的乳酸浓度)和n(希尔系数)分别为20 mM和1.3(n = 5)。即使在存在2 mM ATP的情况下,乳酸也能激活KATP通道。乳酸还使导致最大抑制一半时的ATP浓度Ki从对照时的70 μM(n = 7)显著增加至232 μM(n = 5)。从上述结果可以得出结论,细胞内乳酸直接调节KATP通道,这种调节可能解决在心肌缺血或缺氧期间,膜片钳分离膜片中低Ki与细胞内高ATP浓度之间的差异。

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