乙醇对豚鼠心脏Ca2+和Na+电流的抑制作用

Yoshizumi Habuchi, Taiji Furukawa, Hideo Tanaka, Ling-Ling Lu, Junichiro Morikawa, Manabu Yoshimura
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引用次数: 54

摘要

采用全细胞膜片钳实验对豚鼠心室细胞进行了乙醇对l型Ca2+和快速Na+电流(分别为ICa和INa)的影响。在临床相关浓度为24 mM时,乙醇可轻微但显著缩短动作电位持续时间,使ICa降低7±4%(平均±sd)。该浓度的乙醇不影响INa,但致死浓度的乙醇(80 mM)显著抑制INa(13±5%)。乙醇对INa激活的电压依赖性不受影响,而80 mM乙醇对ICa和240 mM乙醇对INa的抑制作用都伴随着通道可用性曲线向负电位方向移动数mV,表明失活状态的通道更容易受到乙醇的影响。在临床相关浓度下,乙醇对ICa的抑制可能导致负性肌力作用、动作电位缩短和心律失常的发生,而乙醇对INa的抑制的病理生理意义似乎不太重要。
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Ethanol inhibition of Ca2+ and Na+ currents in the guinea-pig heart

The effects of ethanol on L-type Ca2+ and fast Na+ currents (ICa, and INa, respectively) were examined using the whole-cell patch-clamp experiments on guinea-pig ventricular cells. At a clinically relevant concentration of 24 mM, ethanol slightly but significantly shortened the action potential duration, and reduced the ICa by 7 ± 4% (mean ± S.D.). This concentration of ethanol did not affect INa, but a lethal concentration of ethanol (80 mM) significantly inhibited INa by 13 ± 5%. The voltage dependence of INa activation was not affected by ethanol, whereas the inhibitions of ICa by 80 mM ethanol and INa by 240 mM were both accompanied by a several mV shift in the channel availability curve toward more negative potentials, suggesting that the channels in the inactivated state are more susceptible to ethanol. The ICa inhibition by ethanol at clinically relevant concentrations could contribute to a negative inotropic effect, action potential shortening and development of arrhythmias, while the pathophysiological significance of ethanol inhibition of INa seems less important.

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