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Ameliorative effects of Cirsium japonicum extract and main component cirsimaritin in mice model of high-fat diet-induced metabolic dysfunction-associated fatty liver disease.
Che, Denis Nchang; Shin, Jae Young; Kang, Hyun Ju; Cho, Byoung Ok; Park, Ji Hyeon; Wang, Feng; Hao, Suping; Sim, Jae Suk; Sim, Dong Jun; Jang, Seon Il.
Afiliación
  • Che DN; Institute of Health Science Jeonju University Jeonju-si Republic of Korea.
  • Shin JY; Department of Food Science and Technology Jeonbuk National University Jeonju-si Republic of Korea.
  • Kang HJ; Institute of Health Science Jeonju University Jeonju-si Republic of Korea.
  • Cho BO; Institute of Health Science Jeonju University Jeonju-si Republic of Korea.
  • Park JH; Department of Environmental Science and Biotechnology Jeonju University Jeonju-si Republic of Korea.
  • Wang F; Department of Environmental Science and Biotechnology Jeonju University Jeonju-si Republic of Korea.
  • Hao S; Department of Environmental Science and Biotechnology Jeonju University Jeonju-si Republic of Korea.
  • Sim JS; Research Institute Imsil Herbal Medicine Association Imsil Republic of Korea.
  • Sim DJ; Research Institute Imsil Herbal Medicine Association Imsil Republic of Korea.
  • Jang SI; Institute of Health Science Jeonju University Jeonju-si Republic of Korea.
Food Sci Nutr ; 9(11): 6060-6068, 2021 Nov.
Article en En | MEDLINE | ID: mdl-34760237
The objective of this study was to determine biological effects of Cirsium japonicum extract and its main component cirsimaritin on high-fat diet (HFD)-induced metabolic dysfunction-associated fatty liver disease (MAFLD) in a mouse model. Mice were fed with a HFD to induce MAFLD and simultaneously administered with C. japonicum extract (CJE) or cirsimaritin. Various MAFLD biomarkers were evaluated using biological methods. Results demonstrated that triglyceride, aspartate aminotransferase, alanine aminotransferase, and malondialdehyde levels in the liver of mice were significantly reduced upon administration of CJE or cirsimaritin. Treatment with CJE or cirsimaritin also reduced the severity of liver injury in the experimental mouse model of MAFLD by inhibiting hepatic steatosis, oxidative stress, inflammation, and liver fibrosis. These results demonstrate that CJE and cirsimaritin as its main compound have a preventive action against the progression of hepatic steatosis to fibrosis and cirrhosis. Our study suggests that CJE and cirsimaritin might be promising agents for preventing and/or treating MAFLD.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Food Sci Nutr Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Food Sci Nutr Año: 2021 Tipo del documento: Article