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Dietary PUFAs drive diverse system-level changes in lipid metabolism

多不饱和脂肪酸 六烯酸 花生四烯酸 脂质代谢 脂类学 二十碳五烯酸 磷脂酰乙醇胺 生物化学 新陈代谢 脂肪酸 生物 磷脂酰胆碱 化学 食品科学 磷脂
作者
Samuel Furse,Samuel Virtue,Stuart G. Snowden,Antonio Vidal‐Puig,Philip C. Stevenson,Davide Chiarugi,Albert Koulman
出处
期刊:Molecular metabolism [Elsevier]
卷期号:59: 101457-101457 被引量:2
标识
DOI:10.1016/j.molmet.2022.101457
摘要

Polyunsaturated fatty acid (PUFA) supplements have been trialled as a treatment for a number of conditions and produced a variety of results. This variety is ascribed to the supplements, that often comprise a mixture of fatty acids, and to different effects in different organs. In this study, we tested the hypothesis that the supplementation of individual PUFAs has system-level effects that are dependent on the molecular structure of the PUFA.We undertook a network analysis using Lipid Traffic Analysis to identify both local and system-level changes in lipid metabolism using publicly available lipidomics data from a mouse model of supplementation with FA(20:4n-6), FA(20:5n-3), and FA(22:6n-3); arachidonic acid, eicosapentaenoic acid, and docosahexaenoic acid, respectively. Lipid Traffic Analysis is a new computational/bioinformatics tool that uses the spatial distribution of lipids to pinpoint changes or differences in control of metabolism, thereby suggesting mechanistic reasons for differences in observed lipid metabolism.There was strong evidence for changes to lipid metabolism driven by and dependent on the structure of the supplemented PUFA. Phosphatidylcholine and triglycerides showed a change in the variety more than the total number of variables, whereas phosphatidylethanolamine and phosphatidylinositol showed considerable change in both which variables and the number of them, in a highly PUFA-dependent manner. There was also evidence for changes to the endogenous biosynthesis of fatty acids and to both the elongation and desaturation of fatty acids.These results show that the full biological impact of PUFA supplementation is far wider than any single-organ effect and implies that supplementation and dosing with PUFAs require a system-level assessment.

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