Issue 6, 2019

Sinapine reduces non-alcoholic fatty liver disease in mice by modulating the composition of the gut microbiota

Abstract

Non-alcoholic fatty liver disease (NAFLD) is associated with low-grade chronic inflammation and intestinal dysbiosis. In this study, we investigated the potential benefits of sinapine, a rapeseed polyphenol known to exert anti-inflammatory and anti-oxidant effects, on high-fat diet (HFD)-induced NAFLD in C57BL/6 J mice and the underlying mechanisms. Four week-old mice were randomly divided into four groups and fed a low-fat diet (LFD), a HFD, a HFD with common rapeseed oil (HFD + CRO) and a HFD with sinapine in rapeseed oil (HFD + SRO) for 12 weeks. Supplementation with sinapine reduced the body weight of HFD mice by 10.99%, and decreased the levels of TG and LDL-C by 15.67% and 73.62%, respectively. In addition, sinapine also suppressed the intestinal NF-κB and TNF-α expressions and enhanced the adipose tissue IRS-1 expression in the HFD mice (P < 0.05). In terms of effects on the gut microbiota, sinapine induced a decrease in the ratio of Firmicutes to Bacteroidetes and increased the abundance of probiotics, such as Lactobacillaceae, Akkermansiaceae and Blautia, along with metabolite short-chain fatty acid (SCFA)-mediated upregulation of G protein-coupled receptor 43 (GPR43) to inhibit expression of inflammatory factors. Our collective results strongly supported the fact that the utility of sinapine as a prebiotic agent could prevent gut dysbiosis and obesity-related chronic diseases, such as insulin resistance (IR) and NAFLD.

Graphical abstract: Sinapine reduces non-alcoholic fatty liver disease in mice by modulating the composition of the gut microbiota

Supplementary files

Article information

Article type
Paper
Submitted
28 Jan 2019
Accepted
13 May 2019
First published
24 May 2019

Food Funct., 2019,10, 3637-3649

Sinapine reduces non-alcoholic fatty liver disease in mice by modulating the composition of the gut microbiota

Y. Li, J. Li, Q. Su and Y. Liu, Food Funct., 2019, 10, 3637 DOI: 10.1039/C9FO00195F

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