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miR‐96 and autophagy are involved in the beneficial effect of grape seed proanthocyanidins against high‐fat‐diet‐induced dyslipidemia in mice
Author(s) -
Shi Yawei,
Jia Minghan,
Xu Lixia,
Fang Zeng,
Wu Weibin,
Zhang Qi,
Chung Peter,
Lin Ying,
Wang Shenming,
Zhang Yunjian
Publication year - 2019
Publication title -
phytotherapy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.019
H-Index - 129
eISSN - 1099-1573
pISSN - 0951-418X
DOI - 10.1002/ptr.6318
Subject(s) - autophagy , dyslipidemia , downregulation and upregulation , endocrinology , lipid metabolism , chemistry , medicine , foxo1 , lipoprotein , pi3k/akt/mtor pathway , cholesterol , lipid droplet , apoptosis , biology , biochemistry , obesity , protein kinase b , gene
We aimed to investigate the possible signaling pathways underlying the regulation of grape seed proanthocyanidins extracts (GSPE) on lipid metabolism. One hundred male C57BL/6 mice were divided into four groups: control group (normal diet), GSPE group (normal diet + GSPE), high‐fat diet group (HFD), and high‐fat diet plus GSPE (200 mg/kg/day) group (HFD + GSPE). Mice received the diets for 180 days. Body weight and serum lipid levels were measured. Autophagic flux characteristics, such as accumulation of lipids, mitochondria, and autophagosomes in the liver, were detected using transmission electron microscopy. Expression profile of microRNAs (miRNAs) in the liver was determined using RNA microarray and quantitative real time polymerase chain reaction (qRt‐PCR). GSPE significantly decreased the weight gain, serum levels of triglycerides, total cholesterol, and low‐density lipoprotein cholesterol but increased high‐density lipoprotein cholesterol in the HFD mice. Autophagic flux was significantly increased by HFD but decreased by GSPE treatment. GSPE significantly attenuated HFD‐induced miR‐96 upregulation, which in turn reduced the expressions of miR‐96 downstream molecules, FOXO1, mTOR, p‐mTOR, and LC3A/B. These results suggested that the miR‐96 is involved in the protective effect of GSPE against HFD‐induced dyslipidemia. Possible mechanisms might be through mTOR and FOXO1, which facilitate autophagic flux for clearance of lipid accumulation.