Department Physiology, School of Medicine, University of Puerto Rico, San Juan, Puerto Rico.
J Cardiovasc Pharmacol. 2012 Jun;59(6):547-52. doi: 10.1097/FJC.0b013e31824e5273.
Chronic activation of the renin-angiotensin-aldosterone system is a major contributing factor to the pathogenesis and progression of cardiovascular and renal diseases.
To evaluate the role of renin-angiotensin-aldosterone system blockade with aliskiren, a direct renin inhibitor, in the development and progression of dilated cardiomyopathy in the Syrian cardiomyopathic hamster (SCH) model, we treated 1-month-old SCH with aliskiren (10 mg·kg·d) over a 4-month period. For comparative purposes, we also evaluated the effects of the angiotensin receptor blocker valsartan (10 mg·kg·d) and the combination of both drugs. Age-matched golden hamsters were used as controls. Left ventricular end-diastolic volume and end-systolic volume, ejection fraction, and diastolic function were determined by echocardiography. Systolic blood pressure (SBP) was also measured in the left femoral artery by sphygmomanometry.
Results indicate that at 2 months of age, SBP is higher in SCH than in controls, and administration for 1 month of aliskiren, valsartan, or the combination of these drugs normalized SBP in SCH to a similar extent. In 5-month-old SCH, aliskiren improved ejection fraction (from 48.6% ± 5.8% to 69.4% ± 3.2%, n = 5, P < 0.05), left ventricular end-systolic volume (from 0.28 ± 0.06 to 0.10 ± 0.01 mL/100 g body weight), left ventricular end-diastolic volume (from 0.61 ± 0.05 to 0.34 ± 0.02 mL/100 g body weight), and normalized diastolic function (E:A ratio increases from 0.93 ± 0.13 to 1.70 ± 0.03, n = 5, P < 0.05). Similar results were observed with valsartan or the combination of aliskiren and valsartan.
Our results indicate that in this animal model, aliskiren is as effective as valsartan, or the combination of both drugs, in improving diastolic function and in preventing the development of dilated cardiomyopathy. These findings suggest that aliskiren may be used as a monotherapy in heart failure management. Clinical studies, however, are needed to assess the effectiveness of this drug in patients with heart failure.
肾素-血管紧张素-醛固酮系统的慢性激活是心血管和肾脏疾病发病和进展的主要因素。
为了评估直接肾素抑制剂阿利克仑阻断肾素-血管紧张素-醛固酮系统在叙利亚心肌病仓鼠(SCH)模型扩张型心肌病发展和进展中的作用,我们用阿利克仑(10mg·kg·d)治疗 1 月龄的 SCH,为期 4 个月。为了进行比较,我们还评估了血管紧张素受体阻滞剂缬沙坦(10mg·kg·d)和两种药物联合应用的效果。用同龄金黄仓鼠作为对照。通过超声心动图测定左心室舒张末期容积和收缩末期容积、射血分数和舒张功能。通过血压计测量左股动脉的收缩压(SBP)。
结果表明,在 2 月龄时,SCH 的 SBP 高于对照组,用阿利克仑、缬沙坦或两种药物联合治疗 1 个月可使 SCH 的 SBP 恢复到相似水平。在 5 月龄的 SCH 中,阿利克仑提高了射血分数(从 48.6%±5.8%提高到 69.4%±3.2%,n=5,P<0.05)、左心室收缩末期容积(从 0.28±0.06 降低到 0.10±0.01mL/100g 体重)、左心室舒张末期容积(从 0.61±0.05 降低到 0.34±0.02mL/100g 体重)和正常的舒张功能(E:A 比值从 0.93±0.13 提高到 1.70±0.03,n=5,P<0.05)。缬沙坦或阿利克仑与缬沙坦联合应用也观察到类似的结果。
我们的结果表明,在这种动物模型中,阿利克仑与缬沙坦或两种药物联合应用一样,能有效改善舒张功能,预防扩张型心肌病的发生。这些发现表明,阿利克仑可作为心力衰竭治疗的单一疗法。然而,需要进行临床研究来评估该药在心力衰竭患者中的疗效。