首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of propofol and enflurane on action potentials membrane currents and contraction of guinea-pig isolated ventricular myocytes.
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Effects of propofol and enflurane on action potentials membrane currents and contraction of guinea-pig isolated ventricular myocytes.

机译:异丙酚和恩氟烷对豚鼠离体心室肌细胞动作电位膜电流和收缩的影响。

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摘要

1. The effects of two general anaesthetics, propofol and enflurane, on electrical activity and contractions were investigated in single myocytes isolated from guinea-pig ventricles. 2. Propofol and enflurane depressed the plateau and shortened the duration of action potentials. 3. Under voltage-clamp conditions, propofol and enflurane reduced the amplitude of inward calcium current and of additional inward current activated by cytosolic calcium. 4. Contractions (measured with an optical technique) accompanying either action potentials or second inward currents (in response to depolarizations to 0 mV) were reduced by both anaesthetics. The mechanisms for calcium entry during contractions accompanying pulses to positive potentials such as +60 mV are thought to differ from those accompanying second inward currents which are evoked by pulses from -40 to 0 mV. Enflurane enhanced the amplitudes of contractions accompanying pulses to positive potentials; in contrast these contractions were depressed by propofol. 5. In experiments where recovery processes were investigated by use of pairs of voltage-clamp pulses with a variable interval between them, enflurane but not propofol slowed the recovery of contractions and calcium-activated 'tail' currents. These observations are consistent with the hypothesis that enflurane may impair calcium handling by the sarcoplasmic reticulum whereas propofol has little, if any, effect at this site. 6. In conclusion, the actions of propofol and enflurane on second inward currents contribute to their effects on action potentials and contraction. The negative inotropic effect of both anaesthetics may result partly from reduced calcium influx to trigger contraction, and for enflurane, partly from an impairment of calcium handling by the sarcoplasmic reticulum.
机译:1.在从豚鼠心室分离的单个肌细胞中,研究了两种全身麻醉药(异丙酚和恩氟烷)对电活动和收缩的影响。 2.异丙酚和恩氟烷抑制高原并缩短动作电位的持续时间。 3.在电压钳制条件下,丙泊酚和恩氟烷降低了内向钙电流的幅度以及由胞质钙激活的额外内向电流的幅度。 4.两种麻醉剂均减少了伴随动作电位或第二向内电流(响应去极化至0 mV)的收缩(通过光学技术测量)。人们认为,在脉冲伴有正电势(例如+60 mV)的收缩过程中钙进入的机制不同于由-40至0 mV的脉冲引起的伴有第二种内向电流的机制。恩氟烷增强了伴随正电位脉冲的收缩幅度。相反,这些收缩被异丙酚抑制了。 5.在实验中,通过使用成对的电压钳位脉冲之间有可变的间隔来研究恢复过程,安普兰(但不是丙泊酚)减慢了收缩和钙激活的“尾部”电流的恢复。这些观察结果与以下假设相符:环戊烷可能会损害肌浆网对钙的处理,而异丙酚对该部位的影响很小(如果有的话)。 6.总之,丙泊酚和安氟醚在第二次内流中的作用有助于它们对动作电位和收缩的影响。两种麻醉剂的负性肌力作用可能部分是由于钙流入减少导致触发收缩所致;对于安普兰,部分是由于肌浆网对钙处理的损害。

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