dc.description.abstract |
In this study, we aim to investigate whether shikonin prevents against NAFLD. After feeding high-fat diet
(HFD) for 10 weeks, Sprague-Dawley rats were received different doses of shikonin (5mg/kg/day, 10mg/kg/day and
20mg/kg/day) by gavage for the last 12 weeks of a total of 22 weeks of a HFD. Our results showed that total cholesterol
(TC), triacylglycerol (TG), low-density lipoprotein cholesterol, aspartate aminotransferase and alanine aminotransferase
were significantly increased, while high-density lipoprotein cholesterol was decrease, accompanied by hepatic injury and
lipid accumulation in HFD-fed rats. Shikonin treatment attenuated the above biochemical and histopathological changes.
Similarly, HFD-induced the increase of hepatic TC and TG levels were also ameliorated by shikonin treatment.
Furthermore, shikonin observably mitigated HFD-induced the liver fibrosis and the increase of plasminogen activator
inhibitor type 1, connective tissue growth factor, collagen III and IV expression. Additionally, shikonin markedly
inhibited HFD-induced the decrease of proliferator-activated receptor γ (PPARγ) and matrix metalloproteinases-9
(MMP-9) expression and the increase of tissue inhibitor of metalloproteinases-1 (TIMP-1) expression in liver tissue. This
study demonstrates that shikonin ameliorates hepatic lipid dysregulation and fibrosis through PPARγ and MMP-9/TIMP1 axis, suggesting that shikonin may be a potential therapeutic agent for the treatment of NAFLD. |
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