Modulation of IKKβ/NF-κB and TGF-β۱/Smad via Fuzheng Huayu recipe involves in prevention of nutritional steatohepatitis and fibrosis in mice

Objective(s):Fuzheng Huayu recipe (FZHY) exerts significant protective effects against liver fibrosis by strengthening the body’s resistance and removing blood stasis. However, the molecular mechanisms through which FZHY affects liver fibrosis are still unclear. In this study, we examined the expression levels of factors involved in the inhibitor κB kinase-β (IKK-β)/nuclear factor-κB (NF-κB) and transforming growth factor beta ۱ (TGF-β۱)/Smad signaling pathways to elucidate whether FZHY could attenuate nutritional steatohepatitis and fibrosis in mice. Materials and Methods: C۵۷BL/۶J mice were fed with methionine-choline deficient (MCD) diet for ۸ weeks to induce fibrotic steatohepatitis. FZHY and/or heme oxygenase-۱ (HO-۱) chemical inducer (hemin) were administered to mice. The effects of FZHY alone and in combination with hemin were assessed by comparing the severity of hepatic injury, activation of hepatic stellate cells (HSCs), and the expression of oxidative stress, inflammation and fibrogenesis related genes. Results: Administration of FZHY, hemin and FZHY plus hemin significantly ameliorated liver injury. Additionally, our analysis indicated that administration of these agents significantly attenuated oxidative stress, downregulated the expression of pro-inflammatory and pro-fibrotic genes, including IKK-β, NF-κB, monocyte chemoattractant protein-۱ (MCP-۱), α-smooth muscle actin            (α-SMA), TGF-β۱, Smad۳ and Smad۴, and upregulated the expression of the antifibrogenic gene Smad۷ (P< ۰.۰۰۱). Conclusion: FZHY-containing therapies prevented nutritional steatohepatitis and fibrosis through modulating the expression of factors associated with the IKKβ/NF-κB and TGF-β۱/Smad signaling pathways and oxidative stress related genes.

کلیدواژه ها:

Fuzheng Huayu ، Heme oxygenase-۱ ، Hepatic fibrosis ، IKK-β/NF-κB signaling pathway ، Non-alcoholic steatohepatitis ، TGF-β۱/Smad signaling pathway