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dc.contributor.authorYang, Weijia-
dc.contributor.authorYang, Minchun-
dc.contributor.authorYao, Hui-
dc.contributor.authorMa, Yelin-
dc.contributor.authorRen, Xuanxuan-
dc.contributor.authorTeng and Tao Wang, Long-
dc.date.accessioned2022-10-18T10:41:35Z-
dc.date.available2022-10-18T10:41:35Z-
dc.date.issued2020-11-08-
dc.identifier.citationYang, W., Yang, M., Yao, H., Ma, Y., Ren, X., Teng, L., & Wang, T. (2020). Effects of shikonin from Zicao on high-fat diet-induced nonalcoholic fatty liver disease in rats. Pakistan Journal of Pharmaceutical Sciences, 33(6).en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/13225-
dc.description.abstractIn 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.en_US
dc.language.isoenen_US
dc.publisherKarachi:Pakistan Journal of Pharmaceutical Sciences, university of Karachi.en_US
dc.subjectNonalcoholic fatty liver diseaseen_US
dc.subjectlipid accumulationen_US
dc.subjectliver injuryen_US
dc.subjectfibrosisen_US
dc.subjectshikoninen_US
dc.titleEffects of shikonin from Zicao on high-fat diet-induced nonalcoholic fatty liver disease in ratsen_US
dc.typeArticleen_US
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