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普鲁卡因胺对豚鼠乳头肌跨膜动作电位的影响:受细胞外钾离子浓度的影响

Effect of procainamide on transmembrane action potentials in guinea-pig papillary muscles as affected by external potassium concentration.

作者信息

Sada H, Kojima M, Ban T

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1979 Nov;309(2):179-90. doi: 10.1007/BF00501227.

Abstract

Effects of procainamide (PA), 0.18, 0.37 and 0.74 mmol/l, on the transmembrane potential were studied in isolated guinea-pig papillary muscles, superfused with modified Tyrode's solution (external K concentration, [K]0 = 5.4 mmol/l) at the basic driving rate of 1 Hz. PA, at 0.37 mmol/l, significantly reduced the maximum rate of rise of action potential (Vmax) with no change in the resting potential. When 2.7 mmol/l [K]0 of the superfusate was exchanged for 15 mmol/l [K]0 solution a decrease in Vmax induced by 0.37 mmol/l PA became more prominent with decrease in resting potential. The reduction of Vmax at steady state was less at lower driving rates (0.25 and 0.5 Hz) and more at higher driving rates (2-5 Hz) than at 1 Hz in 2.7, 5.4 and 10.0 mmol/l [K]0 solution. Such changes were enhanced concentration-dependently by PA at 5.4 mmol/l [K]0. Also, the changes became more significant with an increase in [K]0 from 2.7 mmol/l to 5.4 mmol/l and then to 10.0 mmol/l. The recovery process of Vmax proceeded with two components. The time course of the slow component seen in the Vmax of the first response after interruption of basic driving stimulation at 1 Hz, followed an approximate monoexponential function. The time constants were 6.3, 4.4 and 5.8 s in the presence of 0.18, 0.37 and 0.74 mmol/l PA at 5.4 mmol/l [K]0 and 3.4 and 3.7 s both in the presence of 0.37 mmol/l PA at 2.7 and 10.0 mmol/l [K]0. Vmax values after 30 or 60 s interruption of stimulation were 80-92% of the predrug Vmax value at 1 Hz. The time constants of the first component, estimated by the peeling-off methods at the driving rate of 0.1 Hz, were 11, 31 and 5-22 ms in the presence of 0.37 mmol/l at 5.4, 10.0 and 2.7 mmol/l [K]0 and did not differ significantly from the time constants in control preparations. The results were found to be consistent, to a certain extent, with the model proposed by Hondeghem and Katzung (1977).

摘要

在以1Hz的基础驱动频率用改良的台氏液(外部钾浓度,[K]0 = 5.4mmol/L) superfused的离体豚鼠乳头肌中,研究了0.18、0.37和0.74mmol/L的普鲁卡因酰胺(PA)对跨膜电位的影响。0.37mmol/L的PA显著降低了动作电位的最大上升速率(Vmax),而静息电位没有变化。当将superfusate中2.7mmol/L的[K]0换成15mmol/L的[K]0溶液时,0.37mmol/L的PA诱导的Vmax降低随着静息电位的降低而变得更加明显。在2.7、5.4和10.0mmol/L的[K]0溶液中,稳态下Vmax的降低在较低驱动频率(0.25和0.5Hz)时较小,在较高驱动频率(2 - 5Hz)时比在1Hz时更大。在5.4mmol/L的[K]0时,PA浓度依赖性地增强了这种变化。此外,随着[K]0从2.7mmol/L增加到5.4mmol/L,然后增加到10.0mmol/L,这些变化变得更加显著。Vmax的恢复过程有两个成分。在1Hz的基础驱动刺激中断后,第一次反应的Vmax中看到的慢成分的时间进程遵循近似单指数函数。在5.4mmol/L的[K]0时,在存在0.18、0.37和0.74mmol/L的PA时,时间常数分别为6.3、4.4和5.8秒,在2.7和10.0mmol/L的[K]0时,在存在0.37mmol/L的PA时,时间常数均为3.4和3.7秒。刺激中断30或60秒后的Vmax值是1Hz时给药前Vmax值的80 - 92%。通过在0.1Hz的驱动频率下用剥离法估计的第一成分的时间常数,在5.4、10.0和2.7mmol/L的[K]0时,在存在0.37mmol/L时分别为11、31和5 - 22毫秒,与对照制剂中的时间常数没有显著差异。结果在一定程度上与Hondeghem和Katzung(1977)提出的模型一致。 (注:superfused这个词在医学专业文献中可能有特定含义,这里暂按原样保留,未准确翻译其确切意思,因为它可能涉及到医学实验中的具体操作术语。)

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