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丙泊酚和安氟醚对豚鼠离体心室肌细胞单钙通道电流的影响。

The effects of propofol and enflurane on single calcium channel currents of guinea-pig isolated ventricular myocytes.

作者信息

Takahashi H, Puttick R M, Terrar D A

机构信息

University Department of Pharmacology, Oxford.

出版信息

Br J Pharmacol. 1994 Apr;111(4):1147-53. doi: 10.1111/j.1476-5381.1994.tb14865.x.

Abstract
  1. The effects of the anaesthetics, propofol (100 microM) and enflurane (3%, 1.46 mM), on single L type calcium channel currents were investigated in single myocytes isolated from guinea-pig ventricles. Channel activity was recorded from membrane patches by use of the 'cell-attached' patch-clamp technique (pipette solution containing 110 mM BaCl2, 5 microM Bay K 8644, 5 microM HEPES, pH 7.4; temperature 36 degrees C). 2. Channel conductance was calculated from the slope of the relationship between single channel current and membrane potential during step depolarizations to activate the channel over a range of approximately -20 to +20 mV. Neither propofol (6 cells) nor enflurane (7 cells) caused any significant reduction in channel conductance. 3. Both propofol (7 cells) and enflurane (9 cells) decreased the probability of the channel being open during depolarizations to +10 mV (measured from histograms of the fraction of time spent by the channel at different current levels, taking areas under the Gaussian curves fitted to the open and closed components of the distributions to represent the proportion of time spent in the two states). 4. A fraction of the current traces showed no detectable channel openings in response to step depolarizations to +10 mV. Both propofol and enflurane significantly increased the fraction of silent traces. 5. Transitions across a threshold halfway between the open and closed levels were used to define periods spent in the open and closed states. Both propofol (7 cells) and enflurane (9 cells) reduced the mean open times and increased the mean closed times of the calcium channel. 6. Histograms were plotted showing the distributions of times spent by the channels in the open and closed states. Two exponentials were fitted to the open and closed time distributions. Both propofol (7 cells) and enflurane (9 cells) shortened both time constants fitted to the open times and lengthened both time constants fitted to the closed times.7. It is concluded that both propofol and enflurane appear to alter the kinetics of opening and closing of calcium channels to favour shut channels without altering channel conductance. This effect would be expected to result in a reduction of the macroscopic calcium current and thus contribute to the negative inotropic action of these anaesthetics.
摘要
  1. 在从豚鼠心室分离出的单个心肌细胞中,研究了麻醉剂丙泊酚(100微摩尔)和安氟醚(3%,1.46毫摩尔)对单个L型钙通道电流的影响。通过使用“细胞贴附式”膜片钳技术(移液管溶液含有110毫摩尔氯化钡、5微摩尔Bay K 8644、5微摩尔HEPES,pH值7.4;温度36摄氏度)从膜片记录通道活性。2. 在大约-20至+20毫伏范围内进行阶跃去极化以激活通道时,根据单通道电流与膜电位之间关系的斜率计算通道电导。丙泊酚(6个细胞)和安氟醚(7个细胞)均未导致通道电导有任何显著降低。3. 丙泊酚(7个细胞)和安氟醚(9个细胞)均降低了在去极化至+10毫伏期间通道开放的概率(根据通道在不同电流水平下花费时间的分数直方图测量,采用拟合分布的开放和关闭成分的高斯曲线下的面积来表示在两种状态下花费的时间比例)。4. 一部分电流记录在响应去极化至+10毫伏时未显示可检测到的通道开放。丙泊酚和安氟醚均显著增加了无活动记录的比例。5. 跨越开放和关闭水平之间中点阈值的转换用于定义在开放和关闭状态下花费的时间。丙泊酚(7个细胞)和安氟醚(9个细胞)均缩短了钙通道的平均开放时间并增加了平均关闭时间。6. 绘制了直方图,显示通道在开放和关闭状态下花费时间的分布。用两个指数函数拟合开放和关闭时间分布。丙泊酚(7个细胞)和安氟醚(9个细胞)均缩短了拟合开放时间的两个时间常数并延长了拟合关闭时间的两个时间常数。7. 得出结论,丙泊酚和安氟醚似乎都改变了钙通道的开放和关闭动力学,有利于通道关闭而不改变通道电导。预计这种效应会导致宏观钙电流减少,从而促成这些麻醉剂的负性肌力作用。

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