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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

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 a...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565240/
https://www.ncbi.nlm.nih.gov/pubmed/34760237
http://dx.doi.org/10.1002/fsn3.2548
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author 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
author_facet 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
author_sort Che, Denis Nchang
collection PubMed
description 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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spelling pubmed-85652402021-11-09 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 Food Sci Nutr Original Research 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. John Wiley and Sons Inc. 2021-09-01 /pmc/articles/PMC8565240/ /pubmed/34760237 http://dx.doi.org/10.1002/fsn3.2548 Text en © 2021 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
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
Ameliorative effects of Cirsium japonicum extract and main component cirsimaritin in mice model of high‐fat diet‐induced metabolic dysfunction‐associated fatty liver disease
title Ameliorative effects of Cirsium japonicum extract and main component cirsimaritin in mice model of high‐fat diet‐induced metabolic dysfunction‐associated fatty liver disease
title_full Ameliorative effects of Cirsium japonicum extract and main component cirsimaritin in mice model of high‐fat diet‐induced metabolic dysfunction‐associated fatty liver disease
title_fullStr Ameliorative effects of Cirsium japonicum extract and main component cirsimaritin in mice model of high‐fat diet‐induced metabolic dysfunction‐associated fatty liver disease
title_full_unstemmed Ameliorative effects of Cirsium japonicum extract and main component cirsimaritin in mice model of high‐fat diet‐induced metabolic dysfunction‐associated fatty liver disease
title_short Ameliorative effects of Cirsium japonicum extract and main component cirsimaritin in mice model of high‐fat diet‐induced metabolic dysfunction‐associated fatty liver disease
title_sort ameliorative effects of cirsium japonicum extract and main component cirsimaritin in mice model of high‐fat diet‐induced metabolic dysfunction‐associated fatty liver disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565240/
https://www.ncbi.nlm.nih.gov/pubmed/34760237
http://dx.doi.org/10.1002/fsn3.2548
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