Pruett J K, Walle T, Bagwell E E
J Pharmacol Exp Ther. 1977 Jul;202(1):45-54.
This study has determined the propranolol content of Purkinje fibers associated with antiarrhythmic and electrophysiological actions of the drug both in vivo and in vitro. The minimum effective tissue content of propranolol that consistently reversed a sustained ouabain-induced ventrivular tachycardia in vivo after i.v. propranolol was between 6.7 and 11.1 micron g/g of tissue. Propranolol doses producing Purkinje fiber contents of less than 6.7 micron g/g failed to revert the arrhythmia but did ponotropic responses to 0.5 micron g/kg of isoproterenol. The in vivo minimum effective tissue content was produced in isolated Purkinje fibers perfused with Tyrode's solution containing 1.7 X 10(-6) M propranolol. In Purkinje fibers this concentration of propranolol depressed the rate of phase 4 depolarization previously enhanced by ouabain 2.1 X 10(-7) M. Propranolol, 1.7 X 10(-6) M, did not alter membrane responsiveness and only slightly accelerated repolarization at 5 minutes. Propranolol, 0.85 X 10(-6) M, did not significantly depress the ouabain-enhanced rate of phase 4 depolarization but did attenuate the response to epinephrine through beta blockade. This study indicated that the initial direct action of propranolol in reverting a ouabain-induced ventricular tachycardia to a sinus rhythm in the dog is depression of automaticity.
本研究测定了普萘洛尔在体内和体外与该药物抗心律失常及电生理作用相关的浦肯野纤维中的含量。静脉注射普萘洛尔后,在体内持续逆转哇巴因诱导的室性心动过速的普萘洛尔最低有效组织含量在6.7至11.1微克/克组织之间。产生低于6.7微克/克浦肯野纤维含量的普萘洛尔剂量未能逆转心律失常,但对0.5微克/千克异丙肾上腺素产生了变时性反应。在含有1.7×10⁻⁶ M普萘洛尔的台氏液灌注的离体浦肯野纤维中产生了体内最低有效组织含量。在浦肯野纤维中,这种浓度的普萘洛尔抑制了先前由2.1×10⁻⁷ M哇巴因增强的4期去极化速率。1.7×10⁻⁶ M的普萘洛尔不会改变膜反应性,仅在5分钟时略微加速复极化。0.85×10⁻⁶ M的普萘洛尔不会显著抑制哇巴因增强的4期去极化速率,但确实通过β受体阻滞减弱了对肾上腺素的反应。这项研究表明,普萘洛尔在将犬哇巴因诱导的室性心动过速恢复为窦性心律时的初始直接作用是抑制自律性。