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低蛋氨酸饮食限制可改善高脂肪饮食喂养小鼠的肠道微生物群,并降低肠道通透性和炎症。

Dietary methionine restriction improves the gut microbiota and reduces intestinal permeability and inflammation in high-fat-fed mice.

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu 214122, China.

出版信息

Food Funct. 2019 Sep 1;10(9):5952-5968. doi: 10.1039/c9fo00766k. Epub 2019 Sep 2.

Abstract

Methionine-restricted diets (MRD) have been shown to prevent high fat diet (HFD) induced complications including fat accumulation, insulin sensitivity decrease, oxidative stress and inflammation increase. We hypothesized that intestinal microbiota changes may mediate these effects, and this study aims to prove this hypothesis. Mice were fed a normal diet (ND, 0.86% methionine + 4% fat), a HF diet (HFD, 0.86% methionine + 20% fat), or a MRD (0.17% methionine + 20% fat) and euthanized at week 22. Our results showed that the HFD induced fat accumulation and gut microbiota dysbiosis; reduced short-chain fatty acid (SCFA) production; and increased intestinal permeability, inflammatory response, and oxidative stress. The MRD decreased the body weight, body fat rate, and blood glucose and plasma lipid levels; increased the abundance of putative SCFA-producing bacteria Bifidobacterium, Lactobacillus, Bacteroides, Roseburia, Coprococcus, and Ruminococcus and inflammation-inhibiting bacteria Oscillospira and Corynebacterium; and decreased the abundance of inflammation-producing bacteria Desulfovibrio in colonic contents. Moreover, the MRD improved intestinal barrier function, inflammatory response, and oxidative stress, and altered the metabolite levels of colonic contents (such as increasing SCFA and bile acid concentrations); the latter may have contributed to the prevention of HFD-induced obesity. In conclusion, the MRD can improve gut health by regulating the intestinal microbiota and its metabolite profiles in the HFD mice. Reducing methionine intake by simple dietary adjustment may be an effective method to improve intestinal health in animals and humans.

摘要

蛋氨酸限制饮食(MRD)已被证明可预防高脂肪饮食(HFD)引起的并发症,包括脂肪积累、胰岛素敏感性降低、氧化应激和炎症增加。我们假设肠道微生物群的变化可能介导这些作用,本研究旨在证明这一假设。将小鼠喂食正常饮食(ND,0.86%蛋氨酸+4%脂肪)、高脂肪饮食(HFD,0.86%蛋氨酸+20%脂肪)或蛋氨酸限制饮食(MRD,0.17%蛋氨酸+20%脂肪),并在第 22 周处死。我们的结果表明,HFD 诱导脂肪积累和肠道微生物群失调;减少短链脂肪酸(SCFA)的产生;并增加肠道通透性、炎症反应和氧化应激。MRD 降低了体重、体脂肪率和血糖及血浆脂质水平;增加了假定的 SCFA 产生菌双歧杆菌、乳杆菌、拟杆菌、罗斯伯里氏菌、粪肠球菌和真杆菌以及炎症抑制菌颤螺菌和棒状杆菌的丰度;并减少了结肠内容物中炎症产生菌脱硫弧菌的丰度。此外,MRD 改善了肠道屏障功能、炎症反应和氧化应激,并改变了结肠内容物的代谢物水平(如增加 SCFA 和胆汁酸浓度);后者可能有助于预防 HFD 诱导的肥胖。总之,MRD 通过调节 HFD 小鼠的肠道微生物群及其代谢物谱来改善肠道健康。通过简单的饮食调整减少蛋氨酸的摄入可能是改善动物和人类肠道健康的有效方法。

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