Abstract
With pronethalol, quinidine, and reserpine it was necessary to increase the dose of acetylstrophanthidin which produced arrhythmia in combination with vagal stimulation. However, in reserpine-treated animals, quinidine and pronethalol were ineffective. The capability of large doses of acetylstrophanthidin to produce ventricular arrhythmia was not diminished by quinidine, pronethalol, or reserpine. While pronethalol decreased the S-A nodal rate in normal animals, it failed to produce an effect on rate after reserpine pretreatment. Since after catecholamine depletion by reserpine, pronethalol and quinidine did not affect acetylstrophanthidin-induced ventricular arrhythmia, it is suggested that the antidigitalis effect of these agents is related to their actions to diminish adrenergic nervous activity.