Abstract
1. Tetrodotoxin (TTX), at a concentration of less than 10−6 g/ml, had no effect on membrane potential and contraction of isolated, thin ventricular trabeculae of sheep and calf hearts. 10−6 to 2 × 10−5 g/ml TTX decreased the rate of rise, over-shoot, and duration (phase of 90% repolarisation) of the action potential and the amplitude of contraction, without change in the resting potential and the plateau (20% repolarisation phase) of the action potential. Excitation block regularly occurred only with 10−5 to 2×10−5 g/ml TTX. 2. In a solution containing Na and TTX (5×10−6-2×10−5 g/ml) graded depolarisation was possible if the preparations were stimulated by square wave pulses of 500 msec duration across a sucrose bridge. In Ca-containing solutions the time-course of the electrotonic potentials showed two steps. The second step of depolarisation (SSD) began when the membrane potential reached−60 to−50 mV (threshold), and tension was initiated at the same level. Contractions reached their steady-state values only after about 5 depolarisations of the same size. There was no difference in the amplitude of contractions (steady-state level) elicited in Tyrode and in Tyrode + TTX. 3. SSD and contraction were dependent on the [Ca]e. Rate of rise (V/sec) and amplitude (mV) of SSD and tension increased with increasing [Ca]e. In Ca-free solutions the electrotonic potentials reached their steady-state levels in one step. No SSD and tension were observed in the absence of Ca, even with reversal of membrane potential. 4. In Tyrode + TTX the SSD was identical with the changes in membrane potential which could be observed in Na-free solution without TTX, but in Na-free solutions, contractions already reached their maximum during the first SSD. 5. SSD in Na-free solution was not blocked by TTX.
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