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.
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