This study investigated whether pulmonary vascular remodelling in hypoxic pulmonary hypertensive rats (10% oxygen; 4 weeks) could be prevented by treatment, during hypoxia, with amlodipine (10 mg/kg/day, p.o.), either alone or in combination with the angiotensin converting enzyme inhibitor, perindopril (30 mg/kg/day, p.o.). Medial thickening of pulmonary arteries (30-500 microm o.d.) was attenuated by amlodipine whereas it was totally prevented by the combination treatment (amlodipine plus perindopril); neomuscularisation of small alveolar arteries (assessed from critical closing pressure in isolated perfused lungs) was not affected. Pulmonary vascular resistance (isolated perfused lungs) was reduced by both treatment regimes but only combination treatment reduced right ventricular hypertrophy. Thus, amlodipine has anti-remodelling properties in pulmonary hypertensive rats. The finding that combining amlodipine with another anti-remodelling drug produced effects on vascular structure that were additive raises the question of whether combination therapy with two different anti-remodelling drugs may be of value in the treatment of patients with hypoxic (and possibly other forms of) pulmonary hypertension.

译文

这项研究调查了在缺氧期间,单独或联合使用氨氯地平 (10 mg/kg/天,p.o.) 是否可以预防低氧性肺动脉高压大鼠 (10% 氧气; 4周) 的肺血管重塑。血管紧张素转化酶抑制剂,培哚普利 (30 mg/kg/天,p.o.)。氨氯地平可减轻肺动脉内侧增厚 (30-500 microm o.d.),而联合治疗 (氨氯地平加培哚普利) 可完全预防; 小肺泡动脉的新血管形成 (根据孤立的灌注肺中的临界闭合压力评估) 不受影响。两种治疗方案均降低了肺血管阻力 (孤立的灌注肺),但仅联合治疗可降低右心室肥大。因此,氨氯地平在肺动脉高压大鼠中具有抗重塑特性。氨氯地平与另一种抗重塑药物联合使用对血管结构产生累加作用的发现提出了一个问题,即与两种不同的抗重塑药物联合治疗在治疗低氧 (可能还有其他形式) 的患者中是否有价值肺动脉高压。

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