Abstract | BACKGROUND: AIM: 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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Authors | Feng Zhu, Yong-Min Li, Ting-Ting Feng, Yue Wu, Hai-Xia Zhang, Guo-Yin Jin, Jian-Ping Liu |
Journal | World journal of gastroenterology
(World J Gastroenterol)
Vol. 25
Issue 24
Pg. 3056-3068
(Jun 28 2019)
ISSN: 2219-2840 [Electronic] United States |
PMID | 31293341
(Publication Type: Journal Article)
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Chemical References |
- Anti-Inflammatory Agents
- Drugs, Chinese Herbal
- Powders
- shigyaku-san
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Topics |
- Animals
- Anti-Inflammatory Agents
(therapeutic use)
- Diet, High-Fat
(adverse effects)
- Disease Models, Animal
- Drug Compounding
(methods)
- Drug Evaluation, Preclinical
- Drugs, Chinese Herbal
(therapeutic use)
- Freeze Drying
- Gastrointestinal Microbiome
(drug effects, physiology)
- Humans
- Male
- Mice
- Non-alcoholic Fatty Liver Disease
(drug therapy, etiology, microbiology)
- Powders
- Treatment Outcome
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