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豚鼠输尿管单个平滑肌细胞瞬时外向电流的特性

Characteristics of transient outward currents in single smooth muscle cells from the ureter of the guinea-pig.

作者信息

Imaizumi Y, Muraki K, Watanabe M

机构信息

Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Nagoya City University, Japan.

出版信息

J Physiol. 1990 Aug;427:301-24. doi: 10.1113/jphysiol.1990.sp018173.

Abstract
  1. Two kinds of transient outward currents were observed upon depolarization of single smooth muscle cells isolated from guinea-pig ureter. The major transient outward current was through Ca2(+)-activated K+ channels (IK(Ca) which had a large conductance (130 pS; 126 mM [K+]i/5.9 mM [K+]o). 2. The smaller transient outward current (ITO) was pharmacologically separated from other membrane currents in the presence of 1 mM-Cd2+ and 2 mM-tetraethylammonium(TEA+) and was selectively blocked by 3 mM-4-aminopyridine. It peaked (approximately 200 pA) within 10 ms upon depolarization from -80 to +20 mV and its half-inactivation time was approximately 50 ms at +20 mV. Half-maximum voltages (V 1/2) for activation and inactivation were about -8 and -50 mV, respectively, in the presence of 1 mM-Cd2+ and 2 mM-TEA+. The time course of recovery from inactivation of ITO was fitted with a single-exponential function (tau = 100 ms at -80 mV). A tenfold change of [K+]o resulted in a 53 mV change in the reversal potential of the tail of ITO. 3. Cadmium reduced peak ITO and shifted the voltage dependence of activation and inactivation in the positive direction in a concentration-dependent manner. The V 1/2 for inactivation in the absence of Cd2+ was estimated to be approximately -64 mV. 4. Single-channel outward currents which appeared only in the initial part of a depolarizing pulse from about -100 mV were recorded using the cell-attached patch clamp. The decay of the ensemble average of the current was similar to the macroscopic ITO under whole-cell clamp. When the holding potential was less negative, the opening probability of the channel greatly decreased. The channel conductance in normal extracellular medium was 14 pS. 5. In ureter cells ITO resembles A-type current. ITO does not contribute significantly to the repolarization of the action potential but it may regulate membrane excitability by opposing Ca2+ current activated around the threshold of the action potential.
摘要
  1. 对从豚鼠输尿管分离出的单个平滑肌细胞进行去极化时,观察到两种瞬时外向电流。主要的瞬时外向电流是通过Ca2(+)-激活的K+通道(IK(Ca)),其电导较大(130 pS;细胞内[K+]为126 mM/细胞外[K+]为5.9 mM)。2. 较小的瞬时外向电流(ITO)在1 mM - Cd2+和2 mM - 四乙铵(TEA+)存在下,通过药理学方法与其他膜电流分离,并被3 mM - 4 - 氨基吡啶选择性阻断。从 - 80 mV去极化到 + 20 mV后10 ms内达到峰值(约200 pA),在 + 20 mV时其半失活时间约为50 ms。在1 mM - Cd2+和2 mM - TEA+存在下,激活和失活的半数最大电压(V 1/2)分别约为 - 8 mV和 - 50 mV。ITO从失活状态恢复的时间进程符合单指数函数(在 - 80 mV时τ = 100 ms)。细胞外[K+]变化10倍导致ITO尾电流反转电位变化53 mV。3. 镉降低了ITO峰值,并以浓度依赖方式使激活和失活的电压依赖性向正向移动。在无Cd2+时失活的V 1/2估计约为 - 64 mV。4. 使用细胞贴附式膜片钳记录仅在从约 - 100 mV开始的去极化脉冲初始部分出现的单通道外向电流。电流的总体平均值衰减与全细胞膜片钳下的宏观ITO相似。当钳制电位不那么负时,通道的开放概率大大降低。在正常细胞外培养基中通道电导为14 pS。5. 在输尿管细胞中,ITO类似于A 型电流。ITO对动作电位的复极化贡献不大,但它可能通过对抗在动作电位阈值附近激活的Ca2+电流来调节膜兴奋性。

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