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A host-microbiome interaction mediates the opposing effects of omega-6 and omega-3 fatty acids on metabolic endotoxemia

机译:宿主-微生物组相互作用介导了omega-6和omega-3脂肪酸对代谢性内毒素血症的相反作用

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摘要

Metabolic endotoxemia, commonly derived from gut dysbiosis, is a primary cause of chronic low grade inflammation that underlies many chronic diseases. Here we show that mice fed a diet high in omega-6 fatty acids exhibit higher levels of metabolic endotoxemia and systemic low-grade inflammation, while transgenic conversion of tissue omega-6 to omega-3 fatty acids dramatically reduces endotoxemic and inflammatory status. These opposing effects of tissue omega-6 and omega-3 fatty acids can be eliminated by antibiotic treatment and animal co-housing, suggesting the involvement of the gut microbiota. Analysis of gut microbiota and fecal transfer revealed that elevated tissue omega-3 fatty acids enhance intestinal production and secretion of intestinal alkaline phosphatase (IAP), which induces changes in the gut bacteria composition resulting in decreased lipopolysaccharide production and gut permeability, and ultimately, reduced metabolic endotoxemia and inflammation. Our findings uncover an interaction between host tissue fatty acid composition and gut microbiota as a novel mechanism for the anti-inflammatory effect of omega-3 fatty acids. Given the excess of omega-6 and deficiency of omega-3 in the modern Western diet, the differential effects of tissue omega-6 and omega-3 fatty acids on gut microbiota and metabolic endotoxemia provide insight into the etiology and management of today’s health epidemics.
机译:代谢性内毒素血症通常源于肠道营养不良,是引起许多慢性疾病的慢性低度炎症的主要原因。在这里,我们显示,喂食高omega-6脂肪酸饮食的小鼠表现出更高水平的代谢性内毒素血症和全身性低度炎症,而组织omega-6到omega-3脂肪酸的转基因转化显着降低了内毒素血症和炎症状态。组织的omega-6和omega-3脂肪酸的这些相反作用可以通过抗生素治疗和动物共居而消除,这表明肠道微生物群的参与。肠道菌群和粪便转移的分析显示,升高的组织中omega-3脂肪酸可增强肠道产生和肠道碱性磷酸酶(IAP)的分泌,从而引起肠道细菌组成的变化,从而导致脂多糖生成和肠道通透性降低,并最终降低代谢性内毒素血症和炎症。我们的发现揭示了宿主组织脂肪酸组成与肠道菌群之间的相互作用,是一种针对omega-3脂肪酸的抗炎作用的新机制。鉴于现代西方饮食中omega-6的过量和omega-3的缺乏,组织omega-6和omega-3脂肪酸对肠道菌群和代谢性内毒素血症的不同作用为当今健康流行病的病因学和治疗提供了见识。 。

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