Hepatoprotective activity of ethanolic extract of Salix subserrata against CCl4-induced chronic hepatotoxicity in rats

被引:33
|
作者
Wahid, Ahmed [2 ]
Hamed, Ashraf N. [3 ]
Eltahir, Heba M. [1 ]
Abouzied, Mekky M. [1 ,2 ]
机构
[1] Taibah Univ, Dept Pharmacol & Toxicol, Coll Pharm, Medina, Saudi Arabia
[2] Menia Univ, Dept Biochem, Fac Pharm, Al Minya 61519, Egypt
[3] Menia Univ, Dept Pharmacognosy, Fac Pharm, Al Minya 61519, Egypt
关键词
Salix Subserrata; Carbon tetrachloride; Hepatoprotective; Silymarin; Liver injury; NF kappa B; TNF-alpha; ACUTE LIVER-INJURY; CARBON-TETRACHLORIDE; IN-VITRO; FIBROSIS; CANCER; MECHANISMS; EXPRESSION; APOPTOSIS; KNOWLEDGE; NECROSIS;
D O I
10.1186/s12906-016-1238-2
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: The liver performs diverse functions that are essential for life. In the absence of reliable liver protective drugs, a large number of natural medicinal preparations are used for the treatment of liver diseases. Therefore the present study aims to investigate the hepatoprotective effects of Salix subserrata Willd flower ethanolic extract (SFEE) against carbon tetrachloride (CCl4)-induced liver damage. Methods: Rats were divided into 4 groups of 10 animals each. Group I served as the normal healthy control, groups II rats were intoxicated with CCl4 i.p. (0.8 ml/kg body weight CCl4/olive oil, twice weekly for 9 weeks), group III rats received CCl4 i.p. and SFEE orally (150 mg/kg daily) and group IV rats received CCl4 i.p. and Silymarin orally (100 mg/kg, daily). The hepatoprotective potential of SFEE in rats was evaluated by measuring the protein levels of two inflammatory biomarkers; tumor necrosis factor-alpha (TNF-alpha) and nuclear factor kappa-B (NF-kB) in addition to other liver biomarkers. Histopathological changes in the liver were assessed using hematoxylin and eosin staining (HE). Results: The administration of SFEE showed hepatic protection at an oral dose of 150 mg/kg. SFEE significantly reduced the elevated serum levels of intracellular liver enzymes as well as liver biomarkers in comparison to CCl4- intoxicated group. Notably, SFEE significantly reduced the expression levels of TNF-a and NFkB proteins compared to their levels in CCl4 intoxicated group. These findings were confirmed with the histopathological observations, where SFEE was capable of reversing the toxic effects of CCl4 on liver cells compared to that observed in CCl4-intoxicated animals. Conclusion: Our results show that SFEE has potential hepatoprotective effects at 150 mg/kg. These effects can be regarded to the antioxidant and anti-inflammatory properties of the extract.
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页数:10
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