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miR-96 和自噬参与葡萄籽原花青素对高脂饮食诱导的小鼠血脂异常的有益作用。

miR-96 and autophagy are involved in the beneficial effect of grape seed proanthocyanidins against high-fat-diet-induced dyslipidemia in mice.

机构信息

Department of Thyroid, Breast Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

Department of Breast Cancer, Cancer Center, Guangdong General Hospital, Guangzhou, China.

出版信息

Phytother Res. 2019 Apr;33(4):1222-1232. doi: 10.1002/ptr.6318. Epub 2019 Mar 8.

Abstract

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.

摘要

我们旨在研究葡萄籽原花青素提取物(GSPE)调节脂质代谢的可能信号通路。将 100 只雄性 C57BL/6 小鼠分为四组:对照组(正常饮食)、GSPE 组(正常饮食+GSPE)、高脂饮食组(HFD)和高脂饮食加 GSPE(200mg/kg/天)组(HFD+GSPE)。小鼠接受饮食 180 天。测量体重和血清脂质水平。使用透射电子显微镜检测肝脏中脂质、线粒体和自噬体的自噬通量特征。使用 RNA 微阵列和定量实时聚合酶链反应(qRt-PCR)确定肝脏中小 RNA(miRNA)的表达谱。GSPE 可显著降低 HFD 小鼠的体重增加、血清甘油三酯、总胆固醇和低密度脂蛋白胆固醇水平,但增加高密度脂蛋白胆固醇。自噬通量被 HFD 显著增加,但被 GSPE 处理降低。GSPE 显著减弱了 HFD 诱导的 miR-96 上调,进而降低了 miR-96 下游分子 FOXO1、mTOR、p-mTOR 和 LC3A/B 的表达。这些结果表明,miR-96 参与了 GSPE 对 HFD 诱导的血脂异常的保护作用。可能的机制可能是通过 mTOR 和 FOXO1 促进自噬通量清除脂质积累。

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