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BL153 Partially Prevents High-Fat Diet Induced Liver Damage Probably via Inhibition of Lipid Accumulation, Inflammation, and Oxidative Stress

The present study was to investigate whether a magnolia extract, named BL153, can prevent obesity-induced liver damage and identify the possible protective mechanism. To this end, obese mice were induced by feeding with high fat diet (HFD, 60% kcal as fat) and the age-matched control mice were fed w...

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Autores principales: Wang, Jian, Zhang, Chi, Zhang, Zhiguo, Chen, Qiang, Lu, Xuemian, Shao, Minglong, Chen, Liangmiao, Yang, Hong, Zhang, Fangfang, Cheng, Peng, Tan, Yi, Kim, Ki-Soo, Kim, Ki Ho, Wang, Bochu, Kim, Young Heui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997087/
https://www.ncbi.nlm.nih.gov/pubmed/24803983
http://dx.doi.org/10.1155/2014/674690
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author Wang, Jian
Zhang, Chi
Zhang, Zhiguo
Chen, Qiang
Lu, Xuemian
Shao, Minglong
Chen, Liangmiao
Yang, Hong
Zhang, Fangfang
Cheng, Peng
Tan, Yi
Kim, Ki-Soo
Kim, Ki Ho
Wang, Bochu
Kim, Young Heui
author_facet Wang, Jian
Zhang, Chi
Zhang, Zhiguo
Chen, Qiang
Lu, Xuemian
Shao, Minglong
Chen, Liangmiao
Yang, Hong
Zhang, Fangfang
Cheng, Peng
Tan, Yi
Kim, Ki-Soo
Kim, Ki Ho
Wang, Bochu
Kim, Young Heui
author_sort Wang, Jian
collection PubMed
description The present study was to investigate whether a magnolia extract, named BL153, can prevent obesity-induced liver damage and identify the possible protective mechanism. To this end, obese mice were induced by feeding with high fat diet (HFD, 60% kcal as fat) and the age-matched control mice were fed with control diet (10% kcal as fat) for 6 months. Simultaneously these mice were treated with or without BL153 daily at 3 dose levels (2.5, 5, and 10 mg/kg) by gavage. HFD feeding significantly increased the body weight and the liver weight. Administration of BL153 significantly reduced the liver weight but without effects on body weight. As a critical step of the development of NAFLD, hepatic fibrosis was induced in the mice fed with HFD, shown by upregulating the expression of connective tissue growth factor and transforming growth factor beta 1, which were significantly attenuated by BL153 in a dose-dependent manner. Mechanism study revealed that BL153 significantly suppressed HFD induced hepatic lipid accumulation and oxidative stress and slightly prevented liver inflammation. These results suggest that HFD induced fibrosis in the liver can be prevented partially by BL153, probably due to reduction of hepatic lipid accumulation, inflammation and oxidative stress.
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spelling pubmed-39970872014-05-06 BL153 Partially Prevents High-Fat Diet Induced Liver Damage Probably via Inhibition of Lipid Accumulation, Inflammation, and Oxidative Stress Wang, Jian Zhang, Chi Zhang, Zhiguo Chen, Qiang Lu, Xuemian Shao, Minglong Chen, Liangmiao Yang, Hong Zhang, Fangfang Cheng, Peng Tan, Yi Kim, Ki-Soo Kim, Ki Ho Wang, Bochu Kim, Young Heui Oxid Med Cell Longev Research Article The present study was to investigate whether a magnolia extract, named BL153, can prevent obesity-induced liver damage and identify the possible protective mechanism. To this end, obese mice were induced by feeding with high fat diet (HFD, 60% kcal as fat) and the age-matched control mice were fed with control diet (10% kcal as fat) for 6 months. Simultaneously these mice were treated with or without BL153 daily at 3 dose levels (2.5, 5, and 10 mg/kg) by gavage. HFD feeding significantly increased the body weight and the liver weight. Administration of BL153 significantly reduced the liver weight but without effects on body weight. As a critical step of the development of NAFLD, hepatic fibrosis was induced in the mice fed with HFD, shown by upregulating the expression of connective tissue growth factor and transforming growth factor beta 1, which were significantly attenuated by BL153 in a dose-dependent manner. Mechanism study revealed that BL153 significantly suppressed HFD induced hepatic lipid accumulation and oxidative stress and slightly prevented liver inflammation. These results suggest that HFD induced fibrosis in the liver can be prevented partially by BL153, probably due to reduction of hepatic lipid accumulation, inflammation and oxidative stress. Hindawi Publishing Corporation 2014 2014-04-03 /pmc/articles/PMC3997087/ /pubmed/24803983 http://dx.doi.org/10.1155/2014/674690 Text en Copyright © 2014 Jian Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Jian
Zhang, Chi
Zhang, Zhiguo
Chen, Qiang
Lu, Xuemian
Shao, Minglong
Chen, Liangmiao
Yang, Hong
Zhang, Fangfang
Cheng, Peng
Tan, Yi
Kim, Ki-Soo
Kim, Ki Ho
Wang, Bochu
Kim, Young Heui
BL153 Partially Prevents High-Fat Diet Induced Liver Damage Probably via Inhibition of Lipid Accumulation, Inflammation, and Oxidative Stress
title BL153 Partially Prevents High-Fat Diet Induced Liver Damage Probably via Inhibition of Lipid Accumulation, Inflammation, and Oxidative Stress
title_full BL153 Partially Prevents High-Fat Diet Induced Liver Damage Probably via Inhibition of Lipid Accumulation, Inflammation, and Oxidative Stress
title_fullStr BL153 Partially Prevents High-Fat Diet Induced Liver Damage Probably via Inhibition of Lipid Accumulation, Inflammation, and Oxidative Stress
title_full_unstemmed BL153 Partially Prevents High-Fat Diet Induced Liver Damage Probably via Inhibition of Lipid Accumulation, Inflammation, and Oxidative Stress
title_short BL153 Partially Prevents High-Fat Diet Induced Liver Damage Probably via Inhibition of Lipid Accumulation, Inflammation, and Oxidative Stress
title_sort bl153 partially prevents high-fat diet induced liver damage probably via inhibition of lipid accumulation, inflammation, and oxidative stress
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997087/
https://www.ncbi.nlm.nih.gov/pubmed/24803983
http://dx.doi.org/10.1155/2014/674690
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