Dickstein K, Gottlieb S, Fleck E, Kostis J, Levine B, DeKock M, LeJemtel T
Cardiology Division, Central Hospital in Rogaland, Stavanger, Norway.
J Hypertens Suppl. 1994 Jul;12(2):S31-5.
Losartan is a specific angiotensin II receptor antagonist with no agonist properties. This agent permits evaluation of the response to selective angiotensin II antagonism in patients with congestive heart failure.
A study was designed to assess the acute hemodynamic and neurohumoral response to losartan in a controlled, blinded fashion.
Sixty-six patients in New York Heart Association functional class II, III or IV with a radionuclide ejection fraction of < 40% were randomly allocated to treatment with placebo and then sequentially to 5, 10, 25, 75 and 150 mg losartan. Hemodynamic and neurohumoral measurements were obtained at selected times for 24 h following ingestion of a single dose of losartan.
Treatment with losartan led to dose-dependent vasodilation. Mean arterial pressure and systemic vascular resistance decreased progressively up to a dose of 25 mg. The higher doses of 75 and 150 mg did not produce additional vasodilation. Similarly, the decrease in pulmonary capillary wedge pressure was not greater with doses exceeding 25 mg. The increase in the cardiac index was modest and similar for all doses. No variation in the heart rate was observed at any dose. The hemodynamic changes were accompanied by marked neurohumoral changes. Large dose-related increases in plasma renin activity and angiotensin II levels were observed, especially following the 150-mg dose. Moderate reductions occurred in serum aldosterone and plasma noradrenaline. The peak effect for these parameters occurred 4-6 h after the dose, with persistent changes still evident 24 h after the dose.
These data demonstrate that selective blockade of the angiotensin II receptor with losartan causes a favorable vasodilatory and neurohumoral response in patients with heart failure. Further studies are needed to determine the most effective dose in these patients. Nevertheless, losartan should be of substantial clinical use in the management of this large population.
氯沙坦是一种无激动剂特性的特异性血管紧张素II受体拮抗剂。该药物可用于评估充血性心力衰竭患者对选择性血管紧张素II拮抗作用的反应。
设计一项研究,以对照、盲法的方式评估氯沙坦的急性血流动力学和神经体液反应。
66例纽约心脏协会心功能II、III或IV级且放射性核素射血分数<40%的患者被随机分配接受安慰剂治疗,然后依次接受5、10、25、75和150mg氯沙坦治疗。在单次服用氯沙坦后的24小时内,在选定时间进行血流动力学和神经体液测量。
氯沙坦治疗导致剂量依赖性血管舒张。平均动脉压和全身血管阻力在剂量达到25mg时逐渐降低。75mg和150mg的较高剂量未产生额外的血管舒张作用。同样,超过25mg的剂量时肺毛细血管楔压的降低也没有更大幅度。所有剂量下心脏指数的增加均较小且相似。任何剂量下均未观察到心率变化。血流动力学变化伴随着明显的神经体液变化。观察到血浆肾素活性和血管紧张素II水平与剂量相关的大幅增加,尤其是在150mg剂量后。血清醛固酮和血浆去甲肾上腺素适度降低。这些参数的峰值效应在给药后4 - 6小时出现,给药后24小时仍有持续变化。
这些数据表明,氯沙坦选择性阻断血管紧张素II受体可使心力衰竭患者产生有利的血管舒张和神经体液反应。需要进一步研究以确定这些患者的最有效剂量。尽管如此,氯沙坦在这类大量患者的治疗中应具有重要的临床应用价值。