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L-丙氨酸可诱发大鼠肝细胞中单个钙激活钾通道的开放。

L-alanine evokes opening of single Ca2+-activated K+ channels in rat liver cells.

作者信息

Bear C E, Petersen O H

机构信息

Department of Physiology, University of Liverpool, Great Britain.

出版信息

Pflugers Arch. 1987 Oct;410(3):342-4. doi: 10.1007/BF00580288.

Abstract

Cellular uptake of neutral amino acids via Na+ cotransporters is known to be associated with an increased membrane K+ conductance mediated by an unknown mechanism that is essential for avoiding excessive cell swelling. We now demonstrate by patch-clamp single-channel current recording that exposure of rat liver cells to L-alanine, but not the poorly transported D-stereoisomer, evokes opening of single K+ channels and that this effect is reversible upon removal of the amino acid. The nature of the conductance pathways opened in the intact cell by L-alanine has been investigated in cell-free excised membrane patches where it can be shown that the K+-selective channels are opened by Ca2+ acting from the inside of the membrane at a concentration as low as 0.1 microM.

摘要

已知通过钠离子协同转运蛋白进行的中性氨基酸的细胞摄取与膜钾离子电导率增加有关,其通过一种未知机制介导,该机制对于避免细胞过度肿胀至关重要。我们现在通过膜片钳单通道电流记录证明,将大鼠肝细胞暴露于L-丙氨酸而非转运较差的D-立体异构体时,会引起单个钾离子通道开放,并且在去除氨基酸后这种效应是可逆的。在无细胞的切除膜片中研究了L-丙氨酸在完整细胞中打开的电导途径的性质,结果表明钾离子选择性通道在膜内侧低至0.1微摩尔浓度的钙离子作用下开放。

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