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Odd Chain Fatty Acids; New Insights of the Relationship Between the Gut Microbiota, Dietary Intake, Biosynthesis and Glucose Intolerance

机译:奇数链脂肪酸;肠道菌群,饮食摄入,生物合成与葡萄糖耐量之间关系的新见解

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摘要

Recent findings have shown an inverse association between circulating C15:0/C17:0 fatty acids with disease risk, therefore, their origin needs to be determined to understanding their role in these pathologies. Through combinations of both animal and human intervention studies, we comprehensively investigated all possible contributions of these fatty acids from the gut-microbiota, the diet, and novel endogenous biosynthesis. Investigations included an intestinal germ-free study and a C15:0/C17:0 diet dose response study. Endogenous production was assessed through: a stearic acid infusion, phytol supplementation, and a Hacl1(-/-) mouse model. Two human dietary intervention studies were used to translate the results. Finally, a study comparing baseline C15:0/C17:0 with the prognosis of glucose intolerance. We found that circulating C15:0/C17:0 levels were not influenced by the gut-microbiota. The dose response study showed C15:0 had a linear response, however C17:0 was not directly correlated. The phytol supplementation only decreased C17:0. Stearic acid infusion only increased C17:0. Hacl1(-/-) only decreased C17:0. The glucose intolerance study showed only C17:0 correlated with prognosis. To summarise, circulating C15:0 and C17:0 are independently derived; C15:0 correlates directly with dietary intake, while C17:0 is substantially biosynthesized, therefore, they are not homologous in the aetiology of metabolic disease. Our findings emphasize the importance of the biosynthesis of C17:0 and recognizing its link with metabolic disease.
机译:最近的发现表明循环的C15:0 / C17:0脂肪酸与疾病风险之间呈负相关,因此,需要确定其来源以了解其在这些病理中的作用。通过动物和人类干预研究的结合,我们全面研究了肠道微生物群,饮食和新型内源性生物合成中这些脂肪酸的所有可能贡献。研究包括一项肠道无菌研究和一项C15:0 / C17:0饮食剂量反应研究。通过以下方法评估内源性生产:硬脂酸输注,植醇补充和Hacl1(-/-)小鼠模型。两项人类饮食干预研究被用来转化结果。最后,将基线C15:0 / C17:0与葡萄糖耐受不良的预后进行了比较。我们发现循环的C15:0 / C17:0水平不受肠道菌群的影响。剂量反应研究表明C15:0具有线性反应,但是C17:0没有直接相关。植醇补充仅降低了C17:0。硬脂酸注入仅增加C17:0。 Hacl1(-/-)仅降低C17:0。葡萄糖耐量研究显示仅C17:0与预后相关。总而言之,循环C15:0和C17:0是独立导出的; C15:0与饮食摄入量直接相关,而C17:0基本上是生物合成的,因此,它们在代谢疾病的病因学上并不同源。我们的发现强调了C17:0的生物合成的重要性,并认识到C17:0与代谢疾病的联系。

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