Evans D B, Peschka M T, Lee R J, Laffan R J
Eur J Pharmacol. 1976 Jan;35(1):17-27. doi: 10.1016/0014-2999(76)90296-x.
The anti-arrhythmic action of 2,3-cis-1,2,3,4-tetrahydro-5-[(2-hydroxy-3-tert-butylamino)propoxy]2,3-naphthalenediol (nadolol) was evaluated and compared with that of propranolol in several experimental models of cardiac arrhythmias. Both nadolol and propranolol antagonized isoproterenol-induced tachycardia and ouabain-induced arrhythmias in cats, antagonized coronary artery ligation-induced ventricular fibrillation and suppressed ventricular ectopic activity during vagal stimulation in dogs. In contrast to propranolol, nadolol was considerably weaker in suppressing existing digoxin-induced arrhythmias, lacked local anesthetic activity and did not depress the heart in dogs. Because of these findings, it is concluded that the anti-arrhythmic activity of nadolol is apparently related to blockade of beta-adrenergic receptors.
在几种心律失常的实验模型中,对2,3-顺式-1,2,3,4-四氢-5-[(2-羟基-3-叔丁氨基)丙氧基]-2,3-萘二醇(纳多洛尔)的抗心律失常作用进行了评估,并与普萘洛尔进行了比较。纳多洛尔和普萘洛尔均可拮抗猫异丙肾上腺素诱发的心动过速和哇巴因诱发的心律失常,拮抗犬冠状动脉结扎诱发的心室颤动,并抑制迷走神经刺激时犬的室性异位活动。与普萘洛尔不同,纳多洛尔在抑制现有的地高辛诱发的心律失常方面明显较弱,缺乏局部麻醉活性,且对犬心脏无抑制作用。基于这些发现,得出结论:纳多洛尔的抗心律失常活性显然与β-肾上腺素能受体的阻断有关。