Core Metabolomics and Lipidomics Laboratory, Wellcome-MRC Institute of Metabolic Science, University of Cambridge, Addenbrooke's Treatment Centre, Keith Day Road Cambridge, CB2 0QQ, UK; Wellcome-MRC Institute of Metabolic Science and Medical Research Council Metabolic Diseases Unit, University of Cambridge, Addenbrooke's Treatment Centre, Keith Day Road Cambridge, CB2 0QQ, UK; Royal Botanic Gardens, Kew, Kew Green, Richmond, Surrey, TW9 3AE, UK.
Wellcome-MRC Institute of Metabolic Science and Medical Research Council Metabolic Diseases Unit, University of Cambridge, Addenbrooke's Treatment Centre, Keith Day Road Cambridge, CB2 0QQ, UK.
Mol Metab. 2022 May;59:101457. doi: 10.1016/j.molmet.2022.101457. Epub 2022 Feb 9.
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.
多不饱和脂肪酸 (PUFA) 补充剂已被尝试用于治疗多种疾病,并产生了多种结果。这种多样性归因于补充剂,它们通常由脂肪酸混合物组成,并且在不同的器官中产生不同的效果。在这项研究中,我们检验了这样一个假设,即单独补充 PUFAs 会产生依赖于 PUFA 分子结构的系统水平效应。
我们使用脂质流量分析进行网络分析,使用来自补充 FA(20:4n-6)、FA(20:5n-3)和 FA(22:6n-3);花生四烯酸、二十碳五烯酸和二十二碳六烯酸的小鼠模型的公开脂质组学数据,来识别脂质代谢的局部和系统水平变化。脂质流量分析是一种新的计算/生物信息学工具,它使用脂质的空间分布来确定代谢控制的变化或差异,从而为观察到的脂质代谢差异提供机制原因。
有强有力的证据表明,补充的 PUFA 的结构驱动并依赖于脂质代谢的变化。与总变量数相比,磷脂酰胆碱和甘油三酯的变化在种类上有更大的变化,而磷脂酰乙醇胺和磷脂酰肌醇的变化在数量和种类上都有很大的变化,这是高度依赖于 PUFA 的。此外,还存在脂肪酸内源性生物合成以及脂肪酸的延伸和去饱和的变化的证据。
这些结果表明,PUFA 补充的全部生物学影响远远超出任何单一器官的影响,并暗示补充和给 PUFAs 给药需要进行系统水平的评估。