Exercise intervention prevents early aged hypertension-caused cardiac dysfunction through inhibition of cardiac fibrosis

Yi Hong, A. Yang, James K. S. Wong, Kunanya Masodsai, Shin-Da Lee, Yi-Yuan Lin
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引用次数: 5

Abstract

Background: An inappropriate accumulation of fibrillar collagen is a common pathologic feature of early aged hypertensive heart disease, but little information regarding the effects of exercise training on cardiac fibrosis in hypertension is available. The purpose of this study was to evaluate the effects of exercise training on cardiac fibrotic pathways in early aged hypertensive rats. Methods: Masson’s trichrome staining and Western blotting were performed on the excised left ventricle from twenty male spontaneously hypertensive rats at age of 48 weeks, which were randomly divided into either a sedentary hypertensive group (SHR) or exercise hypertensive group (SHR-EX, running on a treadmill running occurred 5 days/week for 60 min/day, for 12 weeks), and from age-matched male Wistar–Kyoto normotensive controls (WKY). Results: Interstitial fibrosis was reduced in the SHR-Ex group when compared with the SHR group. The fibrotic-related protein levels of AT1R, FGF23, LOX-2, TGF-β, CTGF, p-Smad 2/3, MMP-2/TIMP-2, MMP-9/TIMP-1, uPA and collagen I were decreased in the SHR-EX group, when compared with the SHR group. Conclusions: Exercise training suppresses early aged hypertensive heart-induced LOX-2/TGF-β-mediated fibrotic pathways associated with decreasing AT1R and FGF23, which might provide a new therapeutic effect for exercise training to prevent adverse cardiac fibrosis and myocardial abnormalities in early aged hypertension.
运动干预通过抑制心脏纤维化预防早衰高血压引起的心功能障碍
背景:纤维性胶原蛋白的不适当积累是早龄高血压心脏病的常见病理特征,但关于运动训练对高血压患者心脏纤维化的影响的信息很少。本研究旨在探讨运动训练对早龄高血压大鼠心肌纤维化通路的影响。方法:对20只48周龄雄性自发性高血压大鼠切除的左心室进行马氏三色染色和Western blotting,随机分为久坐高血压组(SHR)、运动高血压组(SHR- ex,每周5天,每天60分钟,持续12周)和年龄匹配的雄性Wistar-Kyoto正常对照(WKY)。结果:与SHR组相比,SHR- ex组间质纤维化减轻。与SHR组相比,SHR- ex组纤维化相关蛋白AT1R、FGF23、LOX-2、TGF-β、CTGF、p-Smad 2/3、MMP-2/TIMP-2、MMP-9/TIMP-1、uPA、I型胶原蛋白水平降低。结论:运动训练可抑制早衰高血压心脏诱导的LOX-2/TGF-β介导的纤维化通路,并降低AT1R和FGF23,这可能为运动训练预防早衰高血压不良心肌纤维化和心肌异常提供了新的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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