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2
Conduction, Blockade and Gating in a Ca -activated K Channel Incorporated into Planar Lipid Bilayers.整合于平面脂质双分子层中的钙激活钾通道的传导、阻断与门控
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Currents carried by sodium and potassium ions through the membrane of the giant axon of Loligo.钠和钾离子通过枪乌贼巨大轴突膜所携带的电流。
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Excitation--contraction coupling in smooth muscle cells of the guinea-pig mesenteric artery.豚鼠肠系膜动脉平滑肌细胞中的兴奋-收缩偶联
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Effects of vasopressin on smooth muscle cells of guinea-pig mesenteric vessels.血管加压素对豚鼠肠系膜血管平滑肌细胞的作用。
Br J Pharmacol. 1981 Apr;72(4):673-84. doi: 10.1111/j.1476-5381.1981.tb09148.x.
8
Voltage clamp of single freshly dissociated smooth muscle cells: current-voltage relationships for three currents.单个新鲜解离平滑肌细胞的电压钳制:三种电流的电流-电压关系
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Penetration-induced hyperpolarization as evidence for Ca2+ activation of K+ conductance in isolated smooth muscle cells.穿透诱导的超极化作为离体平滑肌细胞中钾离子电导的钙离子激活证据。
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Passive properties of the membrane of single freshly isolated smooth muscle cells.单个新鲜分离的平滑肌细胞膜的被动特性。
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兔空肠和豚鼠肠系膜动脉单个平滑肌细胞中的钙激活钾通道。

Calcium-activated potassium channels in single smooth muscle cells of rabbit jejunum and guinea-pig mesenteric artery.

作者信息

Benham C D, Bolton T B, Lang R J, Takewaki T

出版信息

J Physiol. 1986 Feb;371:45-67. doi: 10.1113/jphysiol.1986.sp015961.

DOI:10.1113/jphysiol.1986.sp015961
PMID:2422353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1192710/
Abstract

Single-channel studies were made using the patch-clamp technique of K channels in dispersed single smooth muscle cells from rabbit longitudinal jejunal muscle and guinea-pig small (less than 0.2 mm o.d.) mesenteric arteries. In isolated inside-out patches from these two types of smooth muscle cell there was a population of K channels which had single-channel conductances of about 100 pS in near physiological K gradients and about 200 pS with symmetrical 126 mM-K solutions. Their conductance and other properties distinguish them from a K channel of smaller conductance which we have previously described in these cells. The relative permeability of the channel with respect to K was 1.4 Tl:1.0 K:0.7 Rb: less than 0.05 Na: less than 0.05 Cs. Cs (1 mM applied to the outside of the membrane) interfered with inward K movement when the membrane was hyperpolarized. Rb conductance of the channel when both sides of the membrane were exposed to 126 mM-Rb was 30 pS. When the Ca concentration on the inside of the membrane ([Ca]i) was about 10(-9) M, K channel opening was rarely observed and then only at strongly positive potentials. At [Ca]i between 10(-9) M and 10(-7) M mean channel open time increased and the probability of channel opening increased steeply; both were further increased by increasing membrane positivity. At [Ca]i between 10(-6) M and 2.5 mM the channel was mainly in the open state and the probability of channel conducting state often declined with increasing membrane positivity. The effects of varying [Ca]i from 10(-7) M to 2.5 mM on the kinetic activity of a single channel was studied largely in mesenteric artery patches containing one active channel. The distribution of open times could be fitted by a single exponential at low (less than 10(-6) M) [Ca]i but a component of fast openings (to less than 1.0 ms) was observed at all potentials at [Ca]i 2.5 mM. Closed time distribution required the sum of three exponentials to fit it all [Ca]i greater than 10(-7) M; at [Ca]i 10(-6) M or greater evidence of a fourth component, probably caused by Ca block of open channels, was obtained. Raising [Ca]i increased the mean duration of the (long) open state and decreased or had no effect on the duration of short, intermediate, and long mean closed states.

摘要

采用膜片钳技术对来自兔空肠纵行肌和豚鼠小(外径小于0.2mm)肠系膜动脉的分散单个平滑肌细胞中的钾通道进行单通道研究。在这两种类型平滑肌细胞的分离内面向外膜片中,存在一群钾通道,在接近生理钾梯度时单通道电导约为100pS,在对称的126mM - K溶液中约为200pS。它们的电导和其他特性使其与我们之前在这些细胞中描述的较小电导的钾通道相区别。该通道对钾的相对通透性为1.4Tl:1.0K:0.7Rb:小于0.05Na:小于0.05Cs。当膜超极化时,1mM的铯(施加于膜外侧)会干扰钾离子的内向移动。当膜两侧都暴露于126mM - Rb时,该通道的铷电导为30pS。当膜内侧的钙浓度([Ca]i)约为10^(-9)M时,很少观察到钾通道开放,且仅在强正电位时开放。当[Ca]i在10^(-9)M至10^(-7)M之间时,平均通道开放时间增加,通道开放概率急剧增加;两者都随着膜电位正向增加而进一步增加。当[Ca]i在10^(-6)M至2.5mM之间时,通道主要处于开放状态,通道导通状态的概率通常随着膜电位正向增加而下降。在主要含有一个活性通道的肠系膜动脉膜片中,研究了[Ca]i从10^(-7)M变化至2.5mM对单个通道动力学活性的影响。在低(小于10^(-6)M)[Ca]i时,开放时间分布可用单一指数拟合,但在[Ca]i为2.5mM时,在所有电位下均观察到快速开放(至小于1.0ms)的成分。当[Ca]i大于10^(-7)M时,关闭时间分布需要三个指数之和来拟合;当[Ca]i为10^(-6)M或更高时,获得了第四个成分的证据,可能是由开放通道的钙阻滞引起的。提高[Ca]i会增加(长)开放状态的平均持续时间,而缩短或不影响短、中、长平均关闭状态的持续时间。