Long-term oral Asperosaponin VI attenuates cardiac dysfunction, myocardial fibrosis in a rat model of chronic myocardial infarction

被引:35
作者
Li, Chunmei [2 ]
Gao, Yonglin [1 ]
Tian, Jingwei [2 ]
Xing, Yanli [3 ]
Zhu, Haibo [3 ]
Shen, Jingyu [1 ]
机构
[1] Yantai Univ, Sch Life Sci, Yantai 264005, Shandong, Peoples R China
[2] Yantai Univ, Sch Pharm, Yantai 264005, Shandong, Peoples R China
[3] Shandong Luye Res & Dev Nat Drugs Co Ltd, Yantai 264003, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Asperosaponin VI; Cardiac dysfunction; Cardiac fibrosis; Oxidative stress; Inflammation mediators; CONGESTIVE-HEART-FAILURE; OXIDATIVE STRESS; VENTRICULAR-FUNCTION; GENE-EXPRESSION; DIPSACUS-ASPER; ANTIOXIDANT; PROBUCOL; RADICALS; ALPHA; CELLS;
D O I
10.1016/j.fct.2012.01.024
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The aim of the study was to determine the effects of Asperosaponin VI (ASA VI), a triterpene saponin isolated from Dipsacus asper Wall, on chronic myocardial infarction (MI) and possible mechanisms in rats. MI was induced by permanent ligation of the left coronary artery. Twenty-four hours after MI, the rats were administered the extract by gavage (once a day). Six weeks after MI/sham surgery, cardiac dysfunction, infarct size (IS), cardiac fibrosis, hydroxyproline concentration, the oxidative stress parameter and inflammation mediators were examined. The results indicated that ASA VI improved left ventricular systolic pressure (LVSP), left ventricular end-diastolic pressure (LVEDP), dP/dt, heart weight/body weight, right ventricular weight/body weight and lung weight/body weight (P < 0.01, P < 0.05). These were accompanied by the attenuation of cardiac fibrosis, IS and hydroxyproline concentration (P < 0.01, P < 0.05). ASA VI could decrease the levels of tumor necrosis factor-alpha (TNF-alpha) and interleukin 6 (IL-6), but increase IL-10 content (P < 0.01, P < 0.05). Furthermore, it also could raise the activities of catalase, superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), but reduce malonyldialdehyde (MDA) level (P < 0.01, P < 0.05). The results indicated that ASA VI improved cardiac function and myocardial fibrosis from myocardial ischemia injury, and this cardioprotection might be attributed to reduce oxidative stress and regulate inflammation mediators. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1432 / 1438
页数:7
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