首页> 美国卫生研究院文献>The Journal of Physiology >Ionic basis of the different action potential configurations of single guinea-pig atrial and ventricular myocytes.
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Ionic basis of the different action potential configurations of single guinea-pig atrial and ventricular myocytes.

机译:单个豚鼠心房和心室肌细胞不同动作电位构型的离子基础。

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摘要

Single myocardial cells were enzymatically dispersed from guinea-pig atria and ventricles. At 25 degrees C, atrial cell action potentials differed significantly from ventricular cell action potentials in duration (atrial = 141 ms, ventricular = 497 ms) and over-shoot (atrial = +36 mV, ventricular = +42 mV). Action potentials of atrial and ventricular cells responded differently to changes in external K+ concentration ([K+]o). Elevation of [K+]o from 6 to 11 mM depolarized atrial cells but produced no significant change in action potential duration; similar changes in [K+]o depolarized ventricular cells and produced a significant shortening of the action potential duration. Voltage-clamp experiments were performed to investigate the ionic basis underlying the different action potential configurations of single atrial and ventricular myocytes. A single-micropipette voltage-clamp technique was used, employing either extremely small-tip diameter pipettes, without internal cell dialysis (Hume & Giles, 1983), or larger tip diameter pipettes, with internal dialysis (Hamill, Marty, Neher, Sakmann & Sigworth, 1981). Two significant differences in background K+ conductance in single atrial and ventricular myocytes were observed: (i) the isochronal (5 s) current-voltage relationship of single ventricular myocytes exhibited a region of prominent negative slope conductance and elevation of [K+]o produced cross-over; a negative slope conductance region was absent in atrial cells and elevation of [K+]o produced very little cross-over of isochronal current-voltage relationships, and (ii) hyperpolarizing voltage pulses applied from holding potentials of -50 mV elicited inward current in ventricular cells which decayed with time; similar voltage-clamp pulses in atrial cells elicited inward currents which fail to decay. Single K+ channel current measurements confirmed the existence of different resting K+ channel properties in single atrial and ventricular myocytes. Resting K+ channels in both cell types had similar single channel conductances (30-32 pS with [K+]o = 145 mM) but ventricular K+ channels had significantly slower gating kinetics compared to atrial K+ channels (ventricular K+ channel mean open time = 223 ms; atrial K+ channel mean open time = 1 ms at Vr (resting membrane potential) -20 mV). The plateau and duration of the guinea-pig ventricular action potential was insensitive to high concentrations of tetrodotoxin (3 X 10(-5) M) but extremely sensitive to external Ca2+ concentration ([Ca2+]o). The second inward Ca2+ current (iCa) density was estimated in small atrial and ventricular myocytes of similar diameter and length.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:从豚鼠心房和心室酶促分散单个心肌细胞。在25摄氏度下,持续时间(心房= 141 ms,心室= 497 ms)和过冲(心房= +36 mV,心室= +42 mV)时,心房细胞动作电位与心室细胞动作电位显着不同。心房和心室细胞的动作电位对外部K +浓度([K +] o)的变化反应不同。 [K +] o从6到11 mM去极化的心房细胞升高,但动作电位持续时间没有明显变化;在[K +] o去极化的心室细胞中发生类似的变化,并显着缩短了动作电位的持续时间。进行电压钳实验以研究单个心房和心室肌细胞不同动作电位构型的离子基础。使用了一种单微量移液器电压钳技术,采用的是极小尖端直径的移液器,而没有内部细胞透析(Hume&Giles,1983),或者是大尖端直径的移液器,具有内部透析(Hamill,Marty,Neher,Sakmann& Sigworth,1981年)。在单个心房和心室肌细胞中观察到两个显着的背景K +电导率差异:(i)单心室肌细胞的等时(5 s)电流-电压关系显示出显着的负斜率电导率区域和[K +] o产生的交叉-过度;心房细胞中不存在负斜率电导区域,[K +] o的升高几乎不会产生等时电流-电压关系的交叉,并且(ii)保持电位为-50 mV施加的超极化电压脉冲在心室引起内向电流。随时间衰减的细胞;心房细胞中类似的电压钳制脉冲会引起无法衰减的内向电流。单K +通道电流测量结果证实了单个心房和心室肌细胞中存在不同的静止K +通道特性。两种细胞类型中的静息K +通道具有相似的单通道电导率(30-32 pS,[K +] o = 145 mM),但与心房K +通道相比,心室K +通道的门控动力学明显较慢(心室K +通道的平均开放时间= 223 ms ;心房K +通道在Vr(静止膜电位)-20 mV时的平均打开时间= 1 ms。豚鼠心室动作电位的平台期和持续时间对高浓度河豚毒素(3 X 10(-5)M)不敏感,但对外部Ca2 +浓度([Ca2 +] o)极为敏感。在直径和长度相近的小型心房和心室肌细胞中估算出第二向内Ca2 +电流(iCa)(摘要截短为400字)

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