Beneficial effects of houttuynin on ventricular remodeling induced by coronary artery ligation in rats

被引:10
作者
Gao, Yan [1 ]
Gao, Jian Ping [1 ]
Chen, Chang Xun [1 ]
Wang, Hui Lin [1 ]
Guo, Juan [1 ]
Wu, Rong [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Dept Pharmacol, Shanghai 201203, Peoples R China
关键词
Houttuynin; Ventricular remodeling; Corollary artery ligation; Myocardial ischemia; RAAS; Peroxidase; HEART-FAILURE; SODIUM HOUTTUYFONATE; ENDOTHELIAL DYSFUNCTION; ALDOSTERONE; HYPERTROPHY; DISEASE;
D O I
10.1016/j.ejphar.2014.07.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To examine the effects of houttuynin on ventricular remodeling induced by coronary artery ligation in rats and the underlying mechanisms. A rat model of ventricular remodeling was established by left coronary artery ligation (CAL). Rats were randomly divided into four groups: CAL control, CAL plus 40 mg/kg captopril, CAL plus 100 mg/kg houttuynin and sham-operated control. The rats were administered intragastrically with the corresponding drugs or distilled water for 7 weeks. At the end of the experiment, the left ventricular weight index (LVWI) and heart weight index (HWI) were determined. Myocardium tissue was stained with hematoxylin and eosin or picric acid/Sirius red for cardiomyocyte cross-section area or collagen content measurements respectively. The concentrations of angiotensin I (Ang l), angiotensin II (Ang II), aldosterone (ALD) and endothelin-1 (ET-1) in myocardium or serum were detected by radioimmunoassay. The hydroxyproline (Hyp) concentration was measured by alkali hydrolysis. Ultraviolet spectrophotometry was used to determine glutathione peroxidase (GSH-Px) and catalase (CAT) activities in serum Houttuynin significantly diminished LVWI and HWI, decreased Ang I, Ang II, ALD, ET-1 and Hyp concentrations in myocardium or serum, increased NO concentration and GSH-Px, CAT activities after 7 weeks of treatment. Houttuynin could also reduce cardiomyocyte cross-section area and collagen deposition Houttuynin attenuates ventricular remodeling in coronary artery ligation rats by restricting the excessive activation of rennin-angiotensin-aldosterone system (RAAS) and the perox dation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:200 / 208
页数:9
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