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海带多糖通过调节肠道微生物群预防高脂肪饮食诱导的小鼠胰岛素抵抗。

Laminaria japonica polysaccharide prevents high-fat-diet-induced insulin resistance in mice via regulating gut microbiota.

机构信息

School of Food and Biological Engineering, Hefei University of Technology, Hefei 230009, People's Republic of China.

出版信息

Food Funct. 2021 Jun 21;12(12):5260-5273. doi: 10.1039/d0fo02100h. Epub 2021 May 17.

Abstract

Insulin resistance has become a worldwide nutrition and metabolic health problem due to the lack of effective protective agents. Laminaria japonica is a well-known marine vegetable. Purified Laminaria japonica polysaccharide (LJP61A) can inhibit atherosclerosis in high-fat-diet (HFD)-fed mice via ameliorating insulin resistance. In this study, we aimed to clarify the mechanism by which LJP61A ameliorates HFD-induced insulin resistance. The results indicated that HFD-induced insulin resistance, obesity, systematic inflammation, metabolic endotoxemia, and gut permeability in mice could be reduced by LJP61A. Gut microbiota analysis showed that the gut microbiota dysbiosis of HFD-fed mice, especially the reduction in mucin-degrading Akkermansia, could be reversed by LJP61A. Additionally, the reduction in mucin-producing goblet cells in HFD-fed mice could also be reversed by LJP61A. Moreover, insulin resistance, obesity, systematic inflammation, metabolic endotoxemia, and gut microbiota dysbiosis in HFD-fed mice could also be alleviated by faecal transplant from LJP61A-treated mice. Overall, LJP61A might be used as a prebiotic to ameliorate HFD-induced insulin resistance and associated metabolic disorders via regulating gut microbiota, especially Akkermansia.

摘要

由于缺乏有效的保护剂,胰岛素抵抗已成为全球性的营养和代谢健康问题。裙带菜是一种著名的海洋蔬菜。纯化的裙带菜多糖(LJP61A)可通过改善胰岛素抵抗来抑制高脂饮食(HFD)喂养的小鼠发生动脉粥样硬化。本研究旨在阐明 LJP61A 改善 HFD 诱导的胰岛素抵抗的机制。结果表明,LJP61A 可降低 HFD 诱导的胰岛素抵抗、肥胖、全身炎症、代谢性内毒素血症和肠道通透性。肠道微生物组分析表明,HFD 喂养小鼠的肠道微生物组失调,特别是黏蛋白降解阿克曼氏菌减少,可被 LJP61A 逆转。此外,LJP61A 还可逆转 HFD 喂养小鼠中黏蛋白产生的杯状细胞减少。此外,LJP61A 还可减轻 HFD 喂养小鼠的胰岛素抵抗、肥胖、全身炎症、代谢性内毒素血症和肠道微生物组失调。总的来说,LJP61A 可能通过调节肠道微生物群,特别是阿克曼氏菌,作为一种益生元来改善 HFD 诱导的胰岛素抵抗和相关代谢紊乱。

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