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非甾体抗炎药激活兔角膜上皮细胞的全细胞钾电流。

Whole-cell potassium current in rabbit corneal epithelium activated by fenamates.

作者信息

Rae J L, Farrugia G

机构信息

Department of Physiology, Mayo Foundation, Rochester, Minnesota 55905.

出版信息

J Membr Biol. 1992 Jul;129(1):81-97. doi: 10.1007/BF00232057.

Abstract

Rabbit corneal epithelium contains a large-conductance, potassium-selective channel, which is a major contributor to the whole-cell current. In perforated-patch recordings of the macroscopic current, the isolated cells studied had resting voltages of -41 +/- 20 mV and capacitances of 5.8 +/- 2.6 pF (mean +/- SD for n = 255). Activation of the channels was weakly voltage dependent. They opened at about -100 mV and reached an open probability of about 0.2 at +100 mV. The current was blocked by millimolar concentrations of external Ba2+ and quinidine. Diltiazem also blocked when applied to the external surface of the membrane. Nonsteroidal anti-inflammatory agents of the fenamate group were powerful activators of the channel at submillimolar concentrations when applied either to the inside or the outside of the channels. The mechanism of action which leads to his activation is not yet known.

摘要

兔角膜上皮含有一种大电导、钾选择性通道,它是全细胞电流的主要贡献者。在宏观电流的穿孔膜片钳记录中,所研究的分离细胞的静息电压为-41±20 mV,电容为5.8±2.6 pF(n = 255的平均值±标准差)。通道的激活对电压的依赖性较弱。它们在约-100 mV时打开,在+100 mV时开放概率达到约0.2。电流被毫摩尔浓度的外部Ba2+和奎尼丁阻断。地尔硫䓬应用于膜外表面时也会阻断电流。当应用于通道内部或外部时,芬那酸盐类非甾体抗炎药在亚毫摩尔浓度下是该通道的强力激活剂。导致其激活的作用机制尚不清楚。

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