Lupi G A, Urthaler F, James T N
Eur J Cardiol. 1979 May;9(5):345-68.
Verapamil delivered via the sinus node artery exerted a dose-related, exclusively negative chronotropic action at all concentrations studied. Perfusion through the AV node artery during AV junctional rhythm also caused a dose-related negative chronotropic response, but the concentrations required to depress this pacemaker were ten times higher than those required to depress sinus node automaticity. Verapamil administered into the AV node artery during sinus rhythm impaired AV conduction. His bundle electrograms demonstrated that depressed A-V conduction was exclusively located at the A-H level. In 5 out of 10 dogs verapamil (5 to 10 mg) delivered into the septal artery caused an abrupt onset of ventricular fibrillation without premonitory dysrhythmias. Verapamil (except at very high concentrations) did not alter the responsiveness of the sinus node and the AV junction to acetylcholine or norepinephrine, whether administered selectively into the sinus node artery or the AV node artery or released by neural stimulation. Serial injections of verapamil were associated with tachyphylaxis for the direct chronotropic and dromotropic properties of the drug.
通过窦房结动脉给药的维拉帕米在所有研究浓度下均呈现出剂量相关的、完全负性变时作用。在房室交界性心律期间经房室结动脉灌注也会引起剂量相关的负性变时反应,但抑制该起搏点所需的浓度比抑制窦房结自律性所需的浓度高10倍。在窦性心律期间经房室结动脉给药的维拉帕米会损害房室传导。希氏束电图显示,房室传导抑制仅发生在A-H水平。在10只犬中的5只,经间隔动脉给予维拉帕米(5至10毫克)会导致室颤突然发作,且无前驱性心律失常。无论选择性地经窦房结动脉或房室结动脉给药,还是通过神经刺激释放,维拉帕米(除极高浓度外)均不会改变窦房结和房室交界对乙酰胆碱或去甲肾上腺素的反应性。维拉帕米的连续注射与该药物的直接变时和变传导特性的快速耐受性相关。