Lu Jingchao, Liu Fan, Liu Demin, Du Hong, Hao Jie, Yang Xiuchun, Cui Wei
Department of Cardiology, The Second Hospital of Hebei Medical University, Hebei 050000, China.
Department of Cardiology, The Second Hospital of Hebei Medical University, Hebei 050000, China
Exp Biol Med (Maywood). 2016 Jun;241(11):1237-49. doi: 10.1177/1535370216630180. Epub 2016 Feb 22.
The present study aims to study the role of receptor activator of nuclear factor kappa B ligand/receptor activator of nuclear factor kappa B/osteoprotegerin (RANKL/RANK/OPG) system in cardiac hypertrophy in a spontaneous hypertension rat (SHR) model and the effects of amlodipine and atorvastatin intervention. Thirty-six-week-old male SHRs were randomly divided into four groups: 1) SHR control group; 2) amlodipine alone (10 mg/kg/d) group, 3) atorvastatin alone (10 mg/kg/d) group, 4) combination of amlodinpine and atorvastatin (10 mg/kg/d for each) group. Same gender, weight, and age of Wistar-Kyoto (WKY) rats with normal blood pressure were used as normal control. Drugs were administered by oral gavage over 12 weeks. The thicknesses of left ventricle walls, left ventricle weight, and cardiac function were measured by transthoracic echocardiography. Left ventricular pressure and function were assessed by hemodynamic examination. Cardiomyocyte hypertrophy and collagen accumulation in cardiac tissue were measured by hematoxylin and eosin (HE) and Masson staining, respectively. The hydroxyproline content of cardiac tissue was examined by biochemistry technique. RANKL, RANK and OPG mRNA, protein expression and tissue localization were studied by RT-PCR, Immunohistochemistry and Western blot. Treatment with amlodipine or atorvastatin alone significantly decreased left ventricular mass index, cardiomyocyte cross-sectional area and interstitial fibrosis in SHR (each P < 0.05). Moreover, combined amlodipine and atorvastatin treatment induced significant reversal of left ventricular hypertrophy and decreased cardiomyocyte cross-sectional area and interstitial fibrosis in SHR to a greater extent than each agent alone (P < 0.05). Compared with WKY rats, the myocardial expression of RANKL, RANK, and OPG was increased. Both amlodipine and atorvastatin reduced RANKL, RANK, and OPG expression, with the best effects seen with the combination. Based on our results, activation of the RANKL/RANK/OPG system may be an important factor leading to ventricular remodeling in SHR rats. Amlodipine and atorvastatin could improve ventricular remodeling in SHR rats through intervention with the RANKL/RANK/OPG system.
本研究旨在探讨核因子κB受体激活剂配体/核因子κB受体激活剂/骨保护素(RANKL/RANK/OPG)系统在自发性高血压大鼠(SHR)模型心脏肥大中的作用以及氨氯地平和阿托伐他汀干预的效果。将36周龄雄性SHR随机分为四组:1)SHR对照组;2)单用氨氯地平(10mg/kg/d)组;3)单用阿托伐他汀(10mg/kg/d)组;4)氨氯地平和阿托伐他汀联合(各10mg/kg/d)组。选取血压正常、性别、体重和年龄相同的Wistar-Kyoto(WKY)大鼠作为正常对照。通过灌胃给药12周。经胸超声心动图测量左心室壁厚度、左心室重量和心功能。通过血流动力学检查评估左心室压力和功能。分别采用苏木精-伊红(HE)染色和Masson染色测量心脏组织中的心肌细胞肥大和胶原积累。采用生化技术检测心脏组织中的羟脯氨酸含量。通过RT-PCR、免疫组织化学和蛋白质印迹法研究RANKL、RANK和OPG的mRNA、蛋白表达及组织定位。单用氨氯地平或阿托伐他汀治疗可显著降低SHR的左心室质量指数、心肌细胞横截面积和间质纤维化(各P<0.05)。此外,氨氯地平和阿托伐他汀联合治疗诱导SHR左心室肥大显著逆转,且降低心肌细胞横截面积和间质纤维化的程度比单用每种药物更大(P<0.05)。与WKY大鼠相比,RANKL、RANK和OPG的心肌表达增加。氨氯地平和阿托伐他汀均降低RANKL、RANK和OPG表达,联合用药效果最佳。基于我们的结果,RANKL/RANK/OPG系统的激活可能是导致SHR大鼠心室重构的重要因素。氨氯地平和阿托伐他汀可通过干预RANKL/RANK/OPG系统改善SHR大鼠的心室重构。