Chemoprotective effect of omega-3 fatty acids on thioacetamide induced hepatic fibrosis in male rats

被引:27
作者
Al-Attar, Atef M. [1 ]
Al-Rethea, Hayfa A. [1 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Dept Biol Sci, POB 139109, Jeddah 21323, Saudi Arabia
关键词
Hepatic fibrosis; Thioacetamide; Omega-3 fatty acids; Rats; INDUCED LIVER FIBROSIS; POLYUNSATURATED FATTY-ACIDS; ROSEMARY LEAVES EXTRACTS; CARBON-TETRACHLORIDE; CIRRHOSIS; INJURY; MODEL; DRUGS; OLIVE; OIL;
D O I
10.1016/j.sjbs.2016.01.029
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The current study was designed to investigate the possible protective effect of omega-3 fatty acids from fish oil on hepatic fibrosis induced by thioacetamide (TAA) in male rats. The experimental animals were divided into four groups. The first group was received saline solution and served as control. The second group was given 250 mg/kg body weight of TAA. The third group was treated with omega-3 fatty acids and TAA. The fourth group was given saline solution and supplemented with omega-3 fatty acids. Treatment of rats with TAA for three and six weeks resulted in a significant decrease in body weight gain, while the value of liver/body weight ratio was statistically increased. Furthermore, the levels of serum alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, gamma glutamyl transferase and total bilirubin were significantly increased. After three weeks of exposure to only TAA, liver sections showed an abnormal morphology characterized by noticeable fibrosis with the extracellular matrix collagen contents and damage of liver cells' structure. Liver sections from rats treated with only TAA for six weeks revealed an obvious increase in extracellular matrix collagen content and bridging fibrosis. Treating TAA-intoxicated rats with omega-3 fatty acids significantly attenuated the severe physiological and histopathological changes. Finally, the present investigation suggests that omega-3 fatty acids could act against hepatic fibrosis induced by TAA due to its antioxidant properties, thus supporting its use in hepatic fibrosis therapy. (C) 2016 Production and hosting by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:956 / 965
页数:10
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