Hesperidin Prevents Liver Fibrosis in Rats by Decreasing the Expression of Nuclear Factor-KB, Transforming Growth Factor-beta and Connective Tissue Growth Factor

摘要

Background/Aims: To evaluate the antioxidant, immuno-modulatory, antinecrotic and antifibrotic effects of hesperidin on CCI_4-induced cirrhosis. Methods: Liver damage was produced by giving CCI_4 injections (0.4 g/kg, i.p., 3 times per week for 8 weeks) to rats. Hesperidin (200 mg/kg) was administered using gavage. The expression of nuclear factor-kappaB (NF-kappaB), transforming growth factor-beta (TGF-beta), connective tissue growth factor (CTGF), interleukin (IL)-10 and IL-1beta was assessed using Western blotting. Alanine aminotrans-ferase (ALT) and gamma-glutamyl transpeptidase (gamma-GTP) serum activities, glycogen content, reduced/oxidised glutathione (GSH/GSSG) ratio, lipid peroxidation degree and fibrosis (using hydroxyproline content and a histopathological analysis) were measured. Results: CCI_4 increased the enzymatic activities of ALT and gamma-GTP, liver lipid peroxidation, the hydroxyproline content as well as NF-kB, TGF-P, CTGF, IL-1beta and IL-10 levels and decreased the glycogen content andGSH/GSSG ratio. Hesperidin significantly decreased the modifications produced by CCI_4, except in the case of IL-10, which was further increased by the flavone. The group receiving hesperidin alone showed decreases in lipid peroxidation, NF-kB, TGF-beta, CTGF and IL-1beta and an increase in IL-10. The results of the histopathological analysis were in agreement with the biochemical and molecular findings. Conclusions: This study demonstrates that hesperidin prevents experimental necrosis and fibrosis. The action mechanism of hesperidin is associated with its ability to reduce oxidative stress and modulate proinflammatory and profibrotic signals. These results support earlier findings demonstrating the beneficial effect of hesperidin against liver damage.