Regårdh C G, Ek L, Hoffmann K J
J Pharmacokinet Biopharm. 1979 Oct;7(5):471-9. doi: 10.1007/BF01062389.
The plasma levels and the beta-blocking effect of metoprolol and its active metabolite alpha-hydroxymetoprolol have been studied after i.v. bolus injections of the substances to dogs. For both substances the beta-blockade increased with the dose, and there was a linear relationship between percent reduction in exercise heart rate and the logarithm of plasma concentration. The dose of the metabolite, however, had to be 5 times higher than that of metoprolol to induce the same degree of beta-blockade. Because of differences in the volume of distribution, 2.0 liters/kg for alpha-OH-metoprolol and 3.5 liters/kg for metoprolol, the 5 times higher dose of alpha-OH-metoprolol resulted in 10 times higher plasma levels of the metabolite than of metoprolol. alpha-OH-Metoprolol was more slowly eliminated (t1/2 approximately 7.0 hr, total body clearance approximately 3.5 ml-kg-1-min-1) than metoprolol (t 1/2 approximately 2.0 hr, total body clearance approximately 20.0 ml-kg-1-min-1). Approximately 5% of an i.v. dose of metoprolol was metabolized to alpha-OH-metoprolol. The half-life of the endogenously formed metabolite was the same as after an i.v. dose of the compound.
静脉推注美托洛尔及其活性代谢产物α-羟基美托洛尔后,研究了它们在犬体内的血浆水平和β受体阻滞作用。对于这两种物质,β受体阻滞作用均随剂量增加而增强,运动心率降低百分比与血浆浓度的对数之间存在线性关系。然而,代谢产物的剂量必须比美托洛尔高5倍才能诱导相同程度的β受体阻滞。由于分布容积不同,α-羟基美托洛尔为2.0升/千克,美托洛尔为3.5升/千克,α-羟基美托洛尔剂量高5倍导致其血浆水平比美托洛尔高10倍。α-羟基美托洛尔的消除速度比美托洛尔慢(半衰期约7.0小时,全身清除率约3.5毫升·千克⁻¹·分钟⁻¹)(美托洛尔半衰期约2.0小时,全身清除率约20.0毫升·千克⁻¹·分钟⁻¹)。静脉注射剂量的美托洛尔约5%代谢为α-羟基美托洛尔。内源性形成的代谢产物的半衰期与静脉注射该化合物后的半衰期相同。