Wagner F, Jähnchen E, Trenk D
Abteilung für Klinische Pharmakologie, Benedikt Kreutz Rehabilitationszentrum, Bad Krozingen, Federal Republic of Germany.
Eur J Clin Pharmacol. 1989;36(6):579-82. doi: 10.1007/BF00637739.
The beta-adrenoceptor blocking activity of the new Class Ic-antiarrhythmic drug diprafenone has been determined in man in comparison with that of propranolol, using the standardized isoproterenol test. Following placebo, the dose of isoproterenol which increased the heart rate by 25 beats.min-1 (CD25) was 0.84 (0.1-2.72) micrograms (median and range). Two hours following single oral doses of 200 mg diprafenone (3.61 micrograms; 1.53-44.15) or 40 mg propranolol (16.06 micrograms; 9.15-27.04) significantly higher CD25-values were found. The affinity constants for the beta-adrenergic receptors calculated on the basis of free drug in the plasma were similar for propranolol and diprafenone (2.79 vs. 2.60 nM-1, respectively). Thus, diprafenone showed a definite degree of beta-blocking activity in a clinically relevant range of plasma concentrations.
采用标准化的异丙肾上腺素试验,将新型Ic类抗心律失常药物双苯丙胺的β-肾上腺素受体阻断活性与普萘洛尔在人体中的活性进行了比较。服用安慰剂后,使心率增加25次·分钟⁻¹的异丙肾上腺素剂量(CD25)为0.84(0.1 - 2.72)微克(中位数和范围)。单次口服200毫克双苯丙胺(3.61微克;1.53 - 44.15)或40毫克普萘洛尔(16.06微克;9.15 - 27.04)两小时后,发现CD25值显著更高。根据血浆中游离药物计算的普萘洛尔和双苯丙胺对β-肾上腺素受体的亲和常数相似(分别为2.79和2.60 nM⁻¹)。因此,双苯丙胺在临床相关的血浆浓度范围内表现出一定程度的β阻断活性。