Effect of lidocaine and quinidine on steady-state characteristics and recovery kinetics of (dV/dt)max in guinea pig ventricular myocardium.
نویسندگان
چکیده
We studied the effects of quinidine and lidocaine on the steady-state relationship between membrane potential and the maximum rate of rise of the action potential, (dV/dt)max, and on the recovery kinetics of (dV/dt)max in guinea pig papillary muscles. The steady-state relationships were determined in fibers stimulated at 0.2/sec and depolarized with KCl. Recovery kinetics were determined at various resting membrane potentials by assessing (dV/dt)max in progressively earlier premature action potentials. Lidocaine caused a dose-dependent decrease in (dV/dt)max, shifted the curve defining the steady-state relationship along the voltage axis in the direction of more negative potentials, and slowed the recovery kinetics of (dV/dt)max. Quinidine caused a dose-dependent decrease in (dV/dt)max but did not alter the shape of the curves defining either the steady-state relationship or the recovery kinetics of (dV/dt)max. Both drugs depressed membrane responsiveness as determined in premature action potentials originating from incompletely repolarized fibers. Our study indicates that the mechanisms whereby quinidine and lidocaine influence (dV/dt)max are different. It is possible that this difference may underlie some of the differences in the clinical effects of these two drugs.
منابع مشابه
pH - Dependent Effects of Quinidine on the Kinetics of dV / dtmajL in Guinea Pig Ventricular Myocardium
Steady state studies have shown that quinidine is more depressant at low pH. To determine whether changes in pH affect the kinetics of quinidine interaction with the sodium channel, we measured transmembrane potential and dV/dtn,ax in guinea pig papillary muscles mounted in a single sucrose gap. pH was changed from 7.4 to 6.9 by changing either the bicarbonate concentration [HC(V] (25-7.5 mm) o...
متن کاملAntidysrhythmic actions of meobentine sulfate
32. Chen C, Gettes LS, Katzung BG: Effect of lidocaine on steady-state characteristics and recovery kinetics of dV/dt max in guinea pig ventricular myocardium. Circ Res 37:20, 1975. 33. El-Sherif N, Scherlag BJ, Lazzara R, Hope RR: Reentrant ventricular arrhythmias in the late myocardial infarction period. A mechanism of action of lidocaine. Circulation 56:395, 1977. 34. Ruskin JN, Akthar M, Fo...
متن کاملPH-Dependent effects of quinidine on the kinetics of dV/dtmax in guinea pig ventricular myocardium.
Steady state studies have shown that quinidine is more depressant at low pH. To determine whether changes in pH affect the kinetics of quinidine interaction with the sodium channel, we measured transmembrane potential and dV/dtn,ax in guinea pig papillary muscles mounted in a single sucrose gap. pH was changed from 7.4 to 6.9 by changing either the bicarbonate concentration [HC(V] (25-7.5 mm) o...
متن کاملEffects of K+ and K+-induced polarization on (dV/dt)max, threshold potential, and membrane input resistance in guinea pig and cat ventricular myocardium.
We studied the non-membrane potential-dependent effect of K+ on (dV/dt)max and threshold potential in guinea pig and cat ventricular myocardium. Membrane potential (MP) was changed uniformly in segments (length less than or equal to 1.0 mm) of papillary muscles by applying extracellular polarizing current pulses across a single sucrose gap. Control [K+]o was 5.4 mM and test [K+]o values were 2....
متن کاملThe influence of pH on th electrophysiological effects of lidocaine in guinea pig ventricular myocardium.
Lidocaine has been reported to be more depressant in ischemic than normal myocardium. To determine the influence of pH on the electrophysiological effects of lidocaine, we recorded transmembrane potential and dV/dtmul from guinea pig papillary muscles mounted in a single sucrose gap. Recovery kinetics of dV/dtma, were studied by introducing progressively early premature responses during phase 4...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Circulation research
دوره 37 1 شماره
صفحات -
تاریخ انتشار 1975