Nademanee K, Schleman M M, Singh B N, Morganroth J, Reid P R, Stritar J A
Am Heart J. 1984 Oct;108(4 Pt 2):1109-15. doi: 10.1016/0002-8703(84)90590-8.
The antiarrhythmic effect of nadolol, a long-acting, nonselective beta antagonist without intrinsic sympathomimetic or membrane-stabilizing properties, was evaluated in 36 patients with ventricular dysrhythmias as determined by three baseline 24-hour Holter recordings at a time when subjects were receiving placebo. Nadolol was administered once daily at a dose of 40 to 80 mg and increased at weekly intervals to a maximum daily dose of 640 mg. Thereafter the drug was stopped gradually and placebo was given again for a period of 2 weeks. Nadolol was effective in reducing premature ventricular contractions (PVCs) in 17 of 36 patients (48%), in reducing ventricular couplets in 24 of 27 patients (89%), and in reducing nonsustained runs of ventricular tachycardia in all 13 subjects. Serum nadolol levels obtained at dosages resulting in a 75% reduction in PVCs varied from 58 to 853 ng/ml. In the majority of the subjects studied, a nadolol dosage of 160 mg/day or less was effective for arrhythmia suppression.
纳多洛尔是一种长效、非选择性β受体拮抗剂,无内在拟交感活性或膜稳定特性。在36例室性心律失常患者中评估了其抗心律失常作用,这些患者在接受安慰剂治疗时,通过三次基线24小时动态心电图记录确定存在室性心律失常。纳多洛尔每日给药一次,剂量为40至80毫克,每周递增至最大每日剂量640毫克。此后逐渐停药,再次给予安慰剂2周。纳多洛尔在36例患者中的17例(48%)有效减少室性早搏(PVC),在27例患者中的24例(89%)有效减少室性成对搏动,在所有13例患者中有效减少非持续性室性心动过速。在导致PVC减少75%的剂量下测得的血清纳多洛尔水平为58至853纳克/毫升。在大多数研究对象中,每日160毫克或更低剂量的纳多洛尔对心律失常抑制有效。