Protective role of puerarin on lead-induced alterations of the hepatic glutathione antioxidant system and hyperlipidemia in rats

被引:118
|
作者
Liu, Chan-Min [1 ]
Ma, Jie-Qiong [2 ]
Sun, Yun-Zhi [1 ]
机构
[1] Xuzhou Normal Univ, Sch Life Sci, Tangshan New Area, Xuzhou 221116, Jiangsu, Peoples R China
[2] China Univ Min & Technol, Sch Chem Engn, Xuzhou 221008, Jiangsu, Peoples R China
关键词
Puerarin; Lead; Glutathione antioxidant system; Hyperlipidemia; Lipid metabolism; Rat liver; INDUCED OXIDATIVE DAMAGE; DE-NOVO SYNTHESIS; LIPID-PEROXIDATION; INDUCED HEPATOTOXICITY; EXPOSED WORKERS; BENEFICIAL ROLE; DOWN-REGULATION; INORGANIC LEAD; NITRIC-OXIDE; WISTAR RATS;
D O I
10.1016/j.fct.2011.09.007
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Puerarin (PU), a natural flavonoid, has been reported to have many benefits and medicinal properties. The aim of the present study was to investigate the effects of puerarin on hepatic oxidative stress and hyperlipidemia in rats exposed to lead. Our data showed that puerarin significantly prevented lead-induced hepatotoxicity, indicated by both diagnostic indicators of liver damage (serum aminotransferase levels) and histopathological analysis. Moreover, lead-induced profound elevation of ROS production and oxidative stress, as evidenced by increasing of lipid peroxidation level, reducing of GPx, GST, GR and GCL activities and depleting of intracellular reduced GSH level in liver, were suppressed by treatment with puerarin. Furthermore, the increase of serum cholesterol, triglycerides and LDL induced by lead was effectively suppressed by puerarin. The HDL level in the lead treatment rats was also increased by puerarin. Western blot analysis showed that puerarin remarkably inhibited hyperlipidemia by regulating the expression of cholesterol 7a-hydroxylase (CYP7A1), 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) and low-density lipoprotein receptor (LDL-R) in liver of lead treated rats. Altogether, these results suggest that puerarin could protect the lead-induced liver injury and hyperlipidemia by reducing ROS production, renewing the activities of antioxidant enzymes and influencing expression of hepatic lipid biosynthesis and metabolism genes. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3119 / 3127
页数:9
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