Ouabain induces phase 4 depolarization in Purkinje fibers, leading to either increased automaticity or low-amplitude potentials, providing a mechanism for conduction impairment in digitalis toxicity.
Microelectrode technics were used to study effects of ouabain (O), 2x10 –7 moles/liter, on phase 4 of Purkinje fiber (PF) transmembrane potentials (TMP). Perfusion for 25-35 min with O caused an increase in phase 4 depolarization which resulted in either increased automaticity or occurrence of low-amplitude potentials (LAP). Increased automaticity was more frequent when PF had been stretched, when K + o = 2.5 mmoles/liter, and when O caused a marked decrease in resting membrane potential (RMP). LAP occurred at all K + o (2.5, 4.0, and 5.0 mmoles/liter), and were the typical response of unstretched fibers in which RMP had not decreased markedly. The magnitude of the LAP increased at K + o = 4.0 mmoles/liter and at faster stimulus rates. Threshold potential (TP) was decreased to a slightly greater extent than RMP. Although LAP did not result in spontaneous action potentials, superimposition of subthreshold depolarizations on LAP resulted in excitation. Whether O-induced increases in phase 4 slope result in automaticity or LAP depends on interrelationships between RMP, TP, and level of membrane potential reached during phase 4. Although hearts developing LAP due to digitalis toxicity may not demonstrate increased automaticity, the presence of phase 4 depolarization in the form of LAP may cause an impairment of conduction which is dependent on cycle length.
Rosen et al. (1973) studied this question.