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泥螈心脏神经元中产生自发性微小外向电流(SMOCs)的钾钙通道数量。

Number of K(Ca) channels underlying spontaneous miniature outward currents (SMOCs) in mudpuppy cardiac neurons.

作者信息

Scornik F S, Merriam L A, Parsons R L

机构信息

Department of Anatomy and Neurobiology, University of Vermont College of Medicine, Burlington, Vermont 05405, USA.

出版信息

J Neurophysiol. 2001 Jan;85(1):54-60. doi: 10.1152/jn.2001.85.1.54.

Abstract

Spontaneous miniature outward currents (SMOCs) in parasympathetic neurons from mudpuppy cardiac ganglia are caused by activation of TEA- and iberiotoxin-sensitive, Ca(2+)-dependent K(+) (BK) channels. Previously we reported that SMOCs are activated by Ca(2+)-induced Ca(2+) release (CICR) from caffeine- and ryanodine-sensitive intracellular Ca(2+) stores. In the present study, we analyzed the single channel currents that contribute to SMOC generation in mudpuppy cardiac neurons. The slope conductance of BK channels, determined from the I-V relationship of single-channel currents recorded with cell-attached patches in physiological K(+) concentrations, was 84 pS. The evidence supporting the identity of this channel as the channel involved in SMOC generation was its sensitivity to internal Ca(2+), external TEA, and caffeine. In cell-attached patch recordings, 166 microM TEA applied in the pipette reduced single-channel current amplitude by 32%, and bath-applied caffeine increased BK channel activity. The ratio between the averaged SMOC amplitude and the single-channel current amplitude was used to estimate the average number of channels involved in SMOC generation. The estimated number of channels involved in generation of an averaged SMOC ranged from 18 to 23 channels. We also determined that the Po of the BK channels at the peak of a SMOC remains constant at voltages more positive than -20 mV, suggesting that the transient rise in intracellular Ca(2+) from ryanodine-sensitive intracellular stores in the vicinity of the BK channel reached concentrations most likely exceeding 40 microM.

摘要

泥螈心脏神经节副交感神经元中的自发性微小外向电流(SMOCs)是由对四乙铵(TEA)和iberiotoxin敏感的、Ca(2+)依赖性钾(BK)通道的激活所引起的。此前我们报道过,SMOCs是由咖啡因和ryanodine敏感的细胞内Ca(2+)储存库中的Ca(2+)诱导的Ca(2+)释放(CICR)所激活的。在本研究中,我们分析了促成泥螈心脏神经元中SMOC产生的单通道电流。在生理钾浓度下,通过细胞贴附式膜片钳记录的单通道电流的I-V关系所确定的BK通道的斜率电导为84 pS。支持该通道与参与SMOC产生的通道一致的证据是其对细胞内Ca(2+)、细胞外TEA和咖啡因的敏感性。在细胞贴附式膜片钳记录中,移液管中施加166 microM的TEA使单通道电流幅度降低了32%,而浴槽中施加咖啡因则增加了BK通道的活性。平均SMOC幅度与单通道电流幅度之间的比率用于估计参与SMOC产生的通道的平均数量。参与产生平均SMOC的通道数量估计在18至23个通道之间。我们还确定,在电压高于 -20 mV时,SMOC峰值处BK通道的开放概率(Po)保持恒定,这表明BK通道附近对ryanodine敏感的细胞内储存库中细胞内Ca(2+)的瞬时升高达到了最有可能超过40 microM的浓度。

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