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Ethanol extract of Allium fistulosum inhibits development of non-alcoholic fatty liver disease

BACKGROUND/OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease and is closely associated with metabolic syndrome. In the present study, we observed the effect of ethanol extract of Allium fistulosum (EAF) on NAFLD and have suggested the possibility of us...

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Autores principales: Hwang, Jin-Taek, Shin, Eun Ju, Chung, Min-Yu, Park, Jae Ho, Chung, Sangwon, Choi, Hyo-Kyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886962/
https://www.ncbi.nlm.nih.gov/pubmed/29629027
http://dx.doi.org/10.4162/nrp.2018.12.2.110
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author Hwang, Jin-Taek
Shin, Eun Ju
Chung, Min-Yu
Park, Jae Ho
Chung, Sangwon
Choi, Hyo-Kyoung
author_facet Hwang, Jin-Taek
Shin, Eun Ju
Chung, Min-Yu
Park, Jae Ho
Chung, Sangwon
Choi, Hyo-Kyoung
author_sort Hwang, Jin-Taek
collection PubMed
description BACKGROUND/OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease and is closely associated with metabolic syndrome. In the present study, we observed the effect of ethanol extract of Allium fistulosum (EAF) on NAFLD and have suggested the possibility of using EAF as a natural product for application in the development of a treatment for NAFLD. MATERIALS/METHODS: The preventive effect on hepatic lipid accumulation was estimated by using an oleic acid (OA)-induced NAFLD model in vitro and a Western diet (high-fat high-sucrose; WD)-induced obese mouse model. Animals were divided into three groups (n = 7): normal diet group (ND), WD group, and WD plus 1% EAF group. RESULTS: EAF reduced OA-stimulated lipid accumulation in HepG2 cells in the absence of cellular cytotoxicity and significantly blocked transcriptional activation of sterol regulatory element-binding protein 1 and fatty acid synthase genes. Subsequently, we investigated these effects in vivo in mice fed either ND or WD in the presence or absence of EAF supplementation. In comparison to the ND controls, the WD-fed mice exhibited increases in body weight, liver weight, epididymal fat weight, and accumulation of fat in hepatocytes, and these effects were significantly attenuated by EAF supplementation. CONCLUSIONS: Allium fistulosum attenuates the development of NAFLD, and EAF elicits anti-lipogenic activity in liver. Therefore, EAF represents a promising candidate for use in the development of novel therapeutic drugs or drug combinations for the prevention and treatment of NAFLD.
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spelling pubmed-58869622018-04-06 Ethanol extract of Allium fistulosum inhibits development of non-alcoholic fatty liver disease Hwang, Jin-Taek Shin, Eun Ju Chung, Min-Yu Park, Jae Ho Chung, Sangwon Choi, Hyo-Kyoung Nutr Res Pract Original Research BACKGROUND/OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease and is closely associated with metabolic syndrome. In the present study, we observed the effect of ethanol extract of Allium fistulosum (EAF) on NAFLD and have suggested the possibility of using EAF as a natural product for application in the development of a treatment for NAFLD. MATERIALS/METHODS: The preventive effect on hepatic lipid accumulation was estimated by using an oleic acid (OA)-induced NAFLD model in vitro and a Western diet (high-fat high-sucrose; WD)-induced obese mouse model. Animals were divided into three groups (n = 7): normal diet group (ND), WD group, and WD plus 1% EAF group. RESULTS: EAF reduced OA-stimulated lipid accumulation in HepG2 cells in the absence of cellular cytotoxicity and significantly blocked transcriptional activation of sterol regulatory element-binding protein 1 and fatty acid synthase genes. Subsequently, we investigated these effects in vivo in mice fed either ND or WD in the presence or absence of EAF supplementation. In comparison to the ND controls, the WD-fed mice exhibited increases in body weight, liver weight, epididymal fat weight, and accumulation of fat in hepatocytes, and these effects were significantly attenuated by EAF supplementation. CONCLUSIONS: Allium fistulosum attenuates the development of NAFLD, and EAF elicits anti-lipogenic activity in liver. Therefore, EAF represents a promising candidate for use in the development of novel therapeutic drugs or drug combinations for the prevention and treatment of NAFLD. The Korean Nutrition Society and the Korean Society of Community Nutrition 2018-04 2018-03-22 /pmc/articles/PMC5886962/ /pubmed/29629027 http://dx.doi.org/10.4162/nrp.2018.12.2.110 Text en ©2018 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Hwang, Jin-Taek
Shin, Eun Ju
Chung, Min-Yu
Park, Jae Ho
Chung, Sangwon
Choi, Hyo-Kyoung
Ethanol extract of Allium fistulosum inhibits development of non-alcoholic fatty liver disease
title Ethanol extract of Allium fistulosum inhibits development of non-alcoholic fatty liver disease
title_full Ethanol extract of Allium fistulosum inhibits development of non-alcoholic fatty liver disease
title_fullStr Ethanol extract of Allium fistulosum inhibits development of non-alcoholic fatty liver disease
title_full_unstemmed Ethanol extract of Allium fistulosum inhibits development of non-alcoholic fatty liver disease
title_short Ethanol extract of Allium fistulosum inhibits development of non-alcoholic fatty liver disease
title_sort ethanol extract of allium fistulosum inhibits development of non-alcoholic fatty liver disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886962/
https://www.ncbi.nlm.nih.gov/pubmed/29629027
http://dx.doi.org/10.4162/nrp.2018.12.2.110
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