Protective effects of total flavonoids of Bidens bipinnata L. against carbon tetrachloride-induced liver fibrosis in rats

Author:

Yuan Li-ping12,Chen Fei-hu1,Ling Lu2,Bo Hu2,Chen Zhi-wu3,Li Fan3,Zhong Ming-mei1,Xia Li-juan1

Affiliation:

1. College of Pharmacy, Anhui Medical University, Hefei, China 230032

2. Department of Pediatrics, First affiliated hospital of Anhui Medical University, Hefei, China 230022

3. Department of Pharmacology, Anhui Medical University, Hefei, China 230032

Abstract

Abstract Bidens bipinnata L. is well known in China as a traditional Chinese medicine and has been used to treat hepatitis in clinics for many years. In a previous study we found that total flavonoids of Bidens bipinnata L. (TFB) had a protective effect against carbon tetrachloride (CCl4)-induced acute liver injury in mice. Now this study was designed to investigate its therapeutic effect against CCl4-induced liver fibrosis in rats and to determine, in part, its mechanism of action. The liver fibrosis model was established by subcutaneous injection of 50% CCl4 twice a week for 18 weeks. TFB (40, 80 and 160 mg kg−1) was administered by gastrogavage daily from the 9th week. The results showed that TFB (80 and 160 mg kg−1) treatment for 10 weeks significantly reduced the elevated liver index (liver weight/body weight) and spleen index (spleen weight/body weight), elevated levels of serum transaminases (alanine aminotransferase and aspartate aminotransferase), hyaluronic acid, type III procollagen and hepatic hydroxyproline. In addition, TFB markedly inhibited CCl4-induced lipid peroxidation and enhanced the activity of the antioxidant enzymes superoxide dismutase and glutathione peroxidase. Moreover, TFB (80 and 160 mg kg−1) treatment improved the morphologic changes of hepatic fibrosis induced by CCl4 and suppressed nuclear factor (NF)-kB, α-smooth muscle actin (SMA) protein expression and transforming growth factor (TGF)-β1 gene expression in the liver of liver fibrosis of rats. In conclusion, TFB was able to ameliorate liver injury and protect rats from CCl4-induced liver fibrosis by suppressing oxidative stress. This process may be related to inhibiting the induction of NF-kB on hepatic stellate cell activation and the expression of TGF-β1.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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