Reid J L
Gardiner Institute, Department of Medicine and Therapeutics, University of Glasgow, Scotland.
Eur Heart J. 1997 Nov;18 Suppl E:E14-8. doi: 10.1016/s0195-668x(97)90004-x.
Angiotensin converting enzyme inhibitors are established treatment for hypertension and heart failure. There are well documented differences between ACE inhibitors both in physicochemical properties and pharmacokinetics. Pharmacodynamic actions are similar for most members of the ACE inhibitor class but there are compounds with additional effects which may reflect protease inhibition or non-enzyme-directed pharmacological properties. Clinically relevant differences are few and far between, particularly in the treatment of hypertension when the optimal dose and dose intervals are used. In heart failure there may be a role for drugs with additional properties such as neutral endopeptidase inhibition. In addition, ACE inhibitors differ in the profile of blood pressure changes after the first dose. Early haemodynamic changes with a fall in blood pressure in heart failure patients may be disadvantageous in terms of subsequent outcome. Thus the haemodynamic effects of the first dose may be relevant to the choice of ACE inhibitors in heart failure.
血管紧张素转换酶抑制剂是治疗高血压和心力衰竭的既定疗法。血管紧张素转换酶抑制剂在物理化学性质和药代动力学方面存在充分记录的差异。血管紧张素转换酶抑制剂类的大多数成员的药效学作用相似,但有一些化合物具有额外作用,这可能反映了蛋白酶抑制或非酶导向的药理特性。临床上相关的差异很少,尤其是在使用最佳剂量和给药间隔治疗高血压时。在心力衰竭中,具有额外特性(如抑制中性内肽酶)的药物可能会发挥作用。此外,血管紧张素转换酶抑制剂在首剂后的血压变化情况有所不同。心力衰竭患者首剂后早期血压下降的血流动力学变化可能对后续结局不利。因此,首剂的血流动力学效应可能与心力衰竭中血管紧张素转换酶抑制剂的选择有关。