Department of Cardiology, Aarhus University Hospital, Denmark.
Department of Cardiology, Aarhus University Hospital, Denmark.
Int J Cardiol. 2019 Oct 15;293:203-210. doi: 10.1016/j.ijcard.2019.06.065. Epub 2019 Jun 29.
Combined angiotensin II receptor antagonism and neprilysin inhibition by LCZ696 reduces morbidity and mortality in heart failure patients and works by reducing RAAS activity and increasing cGMP levels. This study aims to evaluate the effects of LCZ696 in rats with pulmonary hypertension and right ventricular (RV) failure.
Pulmonary hypertension was induced in rats (n = 34) by combined exposure to the vascular endothelial growth factor-receptor antagonist SU5416 and hypoxia (SuHx). To distinguish pulmonary vascular from cardiac effects, isolated RV failure was induced by pulmonary trunk banding (PTB) in another group of rats (n = 40). In both models, the development of RV dysfunction was verified before randomization to treatment with LCZ696 (60 mg/kg/day) or vehicle for five weeks.
In the SuHx rats, LCZ696 treatment reduced the increase in RV pressure and the development of RV hypertrophy and RV dilatation compared with vehicle treatment. LCZ696 also reduced wall thickness of the smaller pulmonary arteries. In the PTB rats, LCZ696 treatment did not have any effects on RV hypertrophy or function.
Combined angiotensin II receptor antagonism and neprilysin inhibition reduced RV systolic pressure, hypertrophy, and dilatation in rats with pulmonary hypertension. These effects seem secondary to pulmonary vascular changes, including reduced pulmonary vascular remodeling, as similar effects were not seen in rats with isolated RV failure. LCZ696 may have a therapeutic potential in the treatment of pulmonary hypertension.
LCZ696 通过联合抑制血管紧张素 II 受体和 Neprilysin,降低心力衰竭患者的发病率和死亡率,其作用机制是降低 RAAS 活性和增加 cGMP 水平。本研究旨在评估 LCZ696 在肺动脉高压和右心室(RV)衰竭大鼠中的作用。
通过联合给予血管内皮生长因子受体拮抗剂 SU5416 和缺氧诱导大鼠肺动脉高压(n = 34)。为了区分肺动脉和心脏的作用,另一组大鼠(n = 40)通过肺动脉干结扎(PTB)诱导孤立性 RV 衰竭。在这两种模型中,在随机分组接受 LCZ696(60mg/kg/天)或载体治疗五周之前,验证 RV 功能障碍的发展。
在 SuHx 大鼠中,与载体治疗相比,LCZ696 治疗可降低 RV 压力升高和 RV 肥厚及扩张的发展。LCZ696 还降低了较小肺动脉的壁厚度。在 PTB 大鼠中,LCZ696 治疗对 RV 肥厚或功能没有任何影响。
联合血管紧张素 II 受体拮抗和 Neprilysin 抑制可降低肺动脉高压大鼠的 RV 收缩压、肥厚和扩张。这些作用似乎继发于肺血管变化,包括减少肺血管重塑,因为在孤立性 RV 衰竭大鼠中未观察到类似的作用。LCZ696 在肺动脉高压的治疗中可能具有治疗潜力。