Modulatory effects of curcumin, silybin-phytosome and alpha-R-lipoic acid against thioacetamide-induced liver cirrhosis in rats

被引:36
作者
Ali, Shimaa Omar [1 ]
Darwish, Hebatallah Abd El-moeti [1 ]
Ismail, Nabila Abd El-fattah [1 ]
机构
[1] Cairo Univ, Dept Biochem, Fac Pharm, Cairo 11562, Egypt
关键词
Liver cirrhosis; Thioacetamide; Curcumin; Silybin-phytosome; Alpha-R-lipoic acid; Oxidative stress; HEPATIC STELLATE CELLS; OXIDATIVE STRESS; MATRIX METALLOPROTEINASES; GROWTH-FACTOR; FIBROSIS; ACTIVATION; EXPRESSION; INJURY; GLUTATHIONE; DAMAGE;
D O I
10.1016/j.cbi.2014.03.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Liver cirrhosis is the final consequence of a progressive fibrotic process characterized by excessive collagen deposition and destruction of the normal liver architecture. This study aimed to investigate the protective effects of curcumin, silybin-phytosome and alpha-R-lipoic acid against thioacetamide-induced cirrhosis. Male rats were allocated into five groups of which one group received saline and served as normal control. Animals from groups 2-5 were treated with thioacetamide administered intraperitoneally at a dose of 200 mg/kg 3 times per week for 7 weeks. Group 2 was left untreated while groups from 3 to 5 were given a daily oral dose of curcumin, silybin-phytosome or alpha-R-lipoic acid simultaneously with thioacetamide. Increases in hepatic levels of malondialdehyde (MDA) and protein carbonyls (Pr Co) associated with thioacetamide administration were partially blocked in those groups receiving supplements. Glutathione (GSH) depletion, collagen deposition, matrix metalloproteinase-2 (MMP-2) activity, transforming growth factor-beta 1 (TGF-beta 1) level as well as a-smooth muscle actin (alpha-SMA) and heat shock protein-47 (HSP-47) gene expressions were also decreased in response to supplements administration. Serological analysis of liver function and histopathological examination reinforced the results. In conclusion, the present study highlights the antioxidant and the antifibrotic potentials of these supplements against chronic liver diseases caused by ongoing hepatic damage. (c) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:26 / 33
页数:8
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