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两种甾体类抗心律失常药物CCI 22277和ORG 6001对豚鼠心室动作电位最大去极化速率的电压和时间依赖性抑制作用

Voltage- and time-dependent depression of maximum rate of depolarization of guinea-pig ventricular action potentials by two steroidal antiarrhythmic drugs, CCI 22277 and ORG 6001.

作者信息

Campbell T J

出版信息

Br J Pharmacol. 1982 Nov;77(3):541-8. doi: 10.1111/j.1476-5381.1982.tb09329.x.

Abstract

1 The voltage- and time-dependence of the depression of the maximum rate of depolarization (Vmax) by two steroidal anti-arrhythmic drugs, CCI22277 and Org 6001 were studied in guinea-pig ventricle. 2 At normal resting potentials CCI22277 (2 microM and 4 microM) produced very little depression of Vmax at very low driving rates (resting block) but trains of stimuli at interstimulus intervals (ISI) of less than 10,000 ms led to an exponential decline in Vmax to a new plateau over 100-200 beats. 3 This 'rate-dependent block' (RDB) increased with rate over the range ISI=4800 to ISI=200 ms. 4 Org 6001 30 microM and 60 microM produced a similar degree of RDB over the same range of frequencies but the new plateau level of Vmax was reached much more rapidly (20-30 beats) and there was a moderate degree of depression of Vmax in the resting tissue. 5 Recovery from RDB in the presence of both drugs was an exponential process with time constants (tau re) of 80.4 +/- 7.4 s for CCI22277 and 4.6 +/- 0.5 s for Org 6001. 6 Both drugs shifted the steady-state inactivation curve, relating Vmax to resting membrane potential, in the hyperpolarizing direction, implying selective depression of depolarized cells.

摘要
  1. 研究了两种甾体类抗心律失常药物CCI22277和Org 6001对豚鼠心室最大去极化速率(Vmax)抑制的电压和时间依赖性。2. 在正常静息电位下,CCI22277(2 microM和4 microM)在极低驱动速率(静息阻滞)时对Vmax的抑制作用很小,但刺激间隔(ISI)小于10,000 ms的刺激序列会导致Vmax在100 - 200次搏动中呈指数下降至新的平台期。3. 这种“速率依赖性阻滞”(RDB)在ISI = 4800至ISI = 200 ms范围内随速率增加。4. Org 6001(30 microM和60 microM)在相同频率范围内产生相似程度的RDB,但Vmax的新平台水平达到得更快(20 - 30次搏动),并且静息组织中的Vmax有中度抑制。5. 在两种药物存在下从RDB恢复是一个指数过程,CCI22277的时间常数(tau re)为80.4 +/- 7.4 s,Org 6001为4.6 +/- 0.5 s。6. 两种药物均使将Vmax与静息膜电位相关的稳态失活曲线向超极化方向移动,这意味着对去极化细胞有选择性抑制作用。

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