Robinson C, Birkhead J, Crook B, Jennings K, Jewitt D
Br Heart J. 1978 Jan;40(1):14-21. doi: 10.1136/hrt.40.1.14.
Atenolol, a cardioselective beta-blocking agent, at dose levels of 0.03, 0.06, and 0.12 mg/kg intravenously, produced prolongation of atrioventricular nodal conduction in 22 patients with suspected coronary artery disease. In a dose of 0.12 mg/kg body weight atenolol produced significant prolongation of sinus cycle length, sinus node recovery time, atrioventricular node conduction, and the effective and functional refractory periods of the atrium and the atrioventricular node. No significant effects were observed on the His Purkinje system or the effective refractory periods of the ventricle. In these actions atenolol closely resembles propranolol. However, because in contrast to propranolol it increases atrial refractoriness, it may have advantages in the treatment of atrial arrhythmias.
阿替洛尔,一种心脏选择性β受体阻滞剂,静脉注射剂量为0.03、0.06和0.12mg/kg时,可使22例疑似冠心病患者的房室结传导延长。当阿替洛尔剂量为0.12mg/kg体重时,可显著延长窦性周期长度、窦房结恢复时间、房室结传导以及心房和房室结的有效不应期和功能不应期。对希氏-浦肯野系统或心室的有效不应期未观察到显著影响。在这些作用方面,阿替洛尔与普萘洛尔非常相似。然而,与普萘洛尔不同的是,它可增加心房不应期,因此在治疗房性心律失常方面可能具有优势。