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Freeze-dried Si-Ni-San powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease

BACKGROUND: Non-alcoholic fatty liver disease (NAFLD) is a common chronic liver disease worldwide. However, to date, there is no ideal therapy for this disease. AIM: To study the effects of Si-Ni-San freeze-dried powder on high fat diet-induced NAFLD in mice. METHODS: Twenty-four male C57BL/6 mice w...

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Autores principales: Zhu, Feng, Li, Yong-Min, Feng, Ting-Ting, Wu, Yue, Zhang, Hai-Xia, Jin, Guo-Yin, Liu, Jian-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603807/
https://www.ncbi.nlm.nih.gov/pubmed/31293341
http://dx.doi.org/10.3748/wjg.v25.i24.3056
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author Zhu, Feng
Li, Yong-Min
Feng, Ting-Ting
Wu, Yue
Zhang, Hai-Xia
Jin, Guo-Yin
Liu, Jian-Ping
author_facet Zhu, Feng
Li, Yong-Min
Feng, Ting-Ting
Wu, Yue
Zhang, Hai-Xia
Jin, Guo-Yin
Liu, Jian-Ping
author_sort Zhu, Feng
collection PubMed
description BACKGROUND: Non-alcoholic fatty liver disease (NAFLD) is a common chronic liver disease worldwide. However, to date, there is no ideal therapy for this disease. AIM: To study the effects of Si-Ni-San freeze-dried powder on high fat diet-induced NAFLD in mice. METHODS: Twenty-four male C57BL/6 mice were randomized into three groups of eight. The control group (CON) was allowed ad libitum access to a normal chow diet. The high fat diet group (FAT) and Si-Ni-San group (SNS) were allowed ad libitum access to a high fat diet. The SNS group was intragastrically administered Si-Ni-San freeze-dried powder (5.0 g/kg) once daily, and the CON and FAT groups were intragastrically administered distilled water. After 12 wk, body weight, liver index, visceral fat index, serum alanine aminotransferase (ALT), portal lipopoly-saccharide (LPS), liver tumor necrosis factor (TNF)-α and liver triglycerides were measured. Intestinal microbiota were analyzed using a 16S r DNA sequencing technique. RESULTS: Compared with the FAT group, the SNS group exhibited decreased body weight, liver index, visceral fat index, serum ALT, portal LPS, liver TNF-α and liver triglycerides (P < 0.05). Intestinal microbiota analysis showed that the SNS group had different bacterial composition and function compared with the FAT group. In particular, Oscillospira genus was a bacterial biomarker of SNS group samples. CONCLUSION: The beneficial effects of Si-Ni-San freeze-dried powder on high fat diet-induced NAFLD in mice may be associated with its anti-inflammatory and changing intestinal microbiota effects.
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spelling pubmed-66038072019-07-10 Freeze-dried Si-Ni-San powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease Zhu, Feng Li, Yong-Min Feng, Ting-Ting Wu, Yue Zhang, Hai-Xia Jin, Guo-Yin Liu, Jian-Ping World J Gastroenterol Basic Study BACKGROUND: Non-alcoholic fatty liver disease (NAFLD) is a common chronic liver disease worldwide. However, to date, there is no ideal therapy for this disease. AIM: To study the effects of Si-Ni-San freeze-dried powder on high fat diet-induced NAFLD in mice. METHODS: Twenty-four male C57BL/6 mice were randomized into three groups of eight. The control group (CON) was allowed ad libitum access to a normal chow diet. The high fat diet group (FAT) and Si-Ni-San group (SNS) were allowed ad libitum access to a high fat diet. The SNS group was intragastrically administered Si-Ni-San freeze-dried powder (5.0 g/kg) once daily, and the CON and FAT groups were intragastrically administered distilled water. After 12 wk, body weight, liver index, visceral fat index, serum alanine aminotransferase (ALT), portal lipopoly-saccharide (LPS), liver tumor necrosis factor (TNF)-α and liver triglycerides were measured. Intestinal microbiota were analyzed using a 16S r DNA sequencing technique. RESULTS: Compared with the FAT group, the SNS group exhibited decreased body weight, liver index, visceral fat index, serum ALT, portal LPS, liver TNF-α and liver triglycerides (P < 0.05). Intestinal microbiota analysis showed that the SNS group had different bacterial composition and function compared with the FAT group. In particular, Oscillospira genus was a bacterial biomarker of SNS group samples. CONCLUSION: The beneficial effects of Si-Ni-San freeze-dried powder on high fat diet-induced NAFLD in mice may be associated with its anti-inflammatory and changing intestinal microbiota effects. Baishideng Publishing Group Inc 2019-06-28 2019-06-28 /pmc/articles/PMC6603807/ /pubmed/31293341 http://dx.doi.org/10.3748/wjg.v25.i24.3056 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Basic Study
Zhu, Feng
Li, Yong-Min
Feng, Ting-Ting
Wu, Yue
Zhang, Hai-Xia
Jin, Guo-Yin
Liu, Jian-Ping
Freeze-dried Si-Ni-San powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease
title Freeze-dried Si-Ni-San powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease
title_full Freeze-dried Si-Ni-San powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease
title_fullStr Freeze-dried Si-Ni-San powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease
title_full_unstemmed Freeze-dried Si-Ni-San powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease
title_short Freeze-dried Si-Ni-San powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease
title_sort freeze-dried si-ni-san powder can ameliorate high fat diet-induced non-alcoholic fatty liver disease
topic Basic Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603807/
https://www.ncbi.nlm.nih.gov/pubmed/31293341
http://dx.doi.org/10.3748/wjg.v25.i24.3056
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