Schneider M F, Dubois J M
Biophys J. 1986 Sep;50(3):523-30. doi: 10.1016/S0006-3495(86)83490-7.
The effects of benzocaine (0.5-1 mM) on normal Na currents, and on Na current and gating charge movement (Q) of batrachotoxin (BTX)-modified Na channels were analyzed in voltage-clamped frog node of Ranvier. Without BTX treatment the decay of Na current during pulses to between -40 and 0 mV could be decomposed into two exponential components both in the absence and in the presence of benzocaine. Benzocaine did not significantly alter the inactivation time constant of either component, but reduced both their amplitudes. The amplitude of the slow inactivating component was more decreased by benzocaine than the amplitude of the fast one, leading to an apparently faster decline of the overall Na current. After removal of Na inactivation and charge movement immobilization by BTX, benzocaine decreased the amplitude of INa with no change in time course. INa, QON, and QOFF were all reduced by the same factor. The results suggest that the rate of reaction of benzocaine with its receptor is slow compared to the rates of channel activation and inactivation. The differential effects of benzocaine on the two components of Na current inactivation in normal channels can be explained assuming two types of channel with different rates of inactivation and different affinities for the drug.
在电压钳制的蛙类朗飞氏结上,分析了苯佐卡因(0.5 - 1 mM)对正常钠电流以及对经蟾毒素(BTX)修饰的钠通道的钠电流和门控电荷移动(Q)的影响。在未用BTX处理时,向 - 40至0 mV之间的电位脉冲期间钠电流的衰减,在不存在和存在苯佐卡因的情况下均可分解为两个指数成分。苯佐卡因并未显著改变任何一个成分的失活时间常数,但降低了它们的幅度。苯佐卡因对慢失活成分幅度的降低比对快失活成分幅度的降低更多,导致总体钠电流明显更快地下降。在用BTX消除钠失活和电荷移动固定后,苯佐卡因降低了INa的幅度,其时程无变化。INa、QON和QOFF均以相同因子降低。结果表明,与通道激活和失活的速率相比,苯佐卡因与其受体的反应速率较慢。苯佐卡因对正常通道中钠电流失活的两个成分的不同影响,可以通过假设存在两种具有不同失活速率和对该药物不同亲和力的通道来解释。