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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >MDG-1, an Ophiopogon polysaccharide, restrains process of non-alcoholic fatty liver disease via modulating the gut-liver axis
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MDG-1, an Ophiopogon polysaccharide, restrains process of non-alcoholic fatty liver disease via modulating the gut-liver axis

机译:MDG-1,Ophiopogon多糖,通过调节肠肝轴来抑制非酒精性脂肪肝病的过程

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摘要

MDG-1, a beta-D-fructan polysaccharide extracted from the roots of Ophiopogon japonicus, had preventive effect against obesity and hyperlipidemia in high-fat diet (HFD)-induced obesity mice. Interestingly, MDG-1, as an inulin-type fructan, is poorly absorbed and its possible mechanism against lipid disturbance remained unclear. The present study aimed to investigate the benefits of MDG-1 treatment on NAFLD model and elucidate mechanism from the perspective of gut-liver axis, especially about gut microbiota, short chain fatty acids (SCFAs) and hepatic lipid metabolism. In this study, after two months HFD feeding, C57BL/6J male mice were randomly divided into HFD group and various MDG-1 dose group. Results showed that MDG-1 markedly blocked weight gain, and ameliorated lipid accumulation, liver damage and macrovesicular steatosis. MDG-1 could restore gut microbiota balance and increase relative abundance of beneficial bacteria, especially SCFAs-producing bacteria. After degradation and utilization by the gut microbiota, MDG-1 could increase the contents of acetic acid and valeric acid, thus regulating inflammatory responses and hepatic lipid metabolism. Specifically, MDG-1 enhanced expression of hepatic phosphorylation of adenosine monophosphate-activated protein kinase, accompanying by regulating hepatic adipogenesis and adipocyte differentiation, thereby inhibiting progress of NAFLD. Our findings may provide new ways in the treatment of hyperlipidemia and lipid-related metabolic syndrome. (C) 2019 Elsevier B.V. All rights reserved.
机译:MDG-1,从Ophiopogon japonicus的根部提取的β-D-Fructan多糖,对高脂饮食(HFD)诱导的肥胖小鼠的肥胖和高脂血症具有预防效果。有趣的是,MDG-1作为菊粉型果蛋白,吸收很差,并且其对抗脂质干扰的可能机制仍不清楚。本研究旨在探讨MDG-1治疗对NAFLD模型的益处,以及肠肝轴的角度,特别是关于肠道微生物,短链脂肪酸(SCFA)和肝脂代谢。在本研究中,经过两个月的喂养后,将C57BL / 6J雄性小鼠随机分为HFD组和各种MDG-1剂量组。结果表明,MDG-1显着堵塞了重量增益,并且改善了脂质积累,肝损伤和宏观分析。 MDG-1可以恢复肠道微生物群平衡,增加有益细菌的相对丰富,特别是产生SCFA的细菌。在肠道微生物肿瘤降解和利用后,MDG-1可以增加乙酸和戊酸的含量,从而调节炎症反应和肝脂代谢。具体而言,通过调节肝脂肪发生和脂肪细胞分化来伴随腺苷一磷​​酸氨磷酸活性蛋白激酶肝磷酸化的肝磷酸化的表达,从而抑制NAFLD的进展。我们的研究结果可以在治疗高脂血症和脂质相关的代谢综合征的治疗中提供新的方法。 (c)2019 Elsevier B.v.保留所有权利。

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