Central Research Laboratory, The Nisshin OilliO Group, Ltd., 1 Shinmori-cho, Isogo-ku, Yokohama 235-8558, Japan.
Department of Systems Life Sciences, Graduate School of Systems Life Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
J Agric Food Chem. 2020 Oct 28;68(43):11997-12010. doi: 10.1021/acs.jafc.0c04723. Epub 2020 Oct 19.
Several studies in hepatocyte cell lines reported that medium-chain fatty acids (MCFAs) with 6-12 carbons showed different metabolic properties from long-chain fatty acids (LCFAs). However, these studies reported unclear effects of different fatty acid molecules on hepatocyte metabolism. This study is aimed to capture the metabolic kinetics of MCFA assimilation in AML12 cells treated with octanoic acid (FA 8:0), decanoic acid (FA 10:0), or lauric acid (FA12:0) [LCFA; oleic acid (FA 18:1)] metabolic profiling and dynamic metabolome analysis with C-labeling. The concentrations of total ketone bodies in the media of cells treated with FA 8:0 or FA 10:0 were 3.22- or 3.69-fold higher than those obtained with FA 18:1 treatment, respectively. FA 12:0 treatment did not significantly increase ketone body levels compared to DMSO treatment (control), whereas FA 12:0 treatment increased intracellular triacylglycerol (TG) levels 15.4 times compared to the control. Metabolic profiles of FA 12:0-treated samples differed from those of the FA 8:0-treated and FA 10:0-treated samples, suggesting that metabolic assimilation of MCFAs differed significantly depending on the MCFA type. Furthermore, the dynamic metabolome analysis clearly revealed that FA 8:0 was rapidly and quantitatively oxidized to acetyl-CoA and assimilated into ketone bodies, citrate cycle intermediates, and glucogenic amino acids but not readily into TGs.
几项在肝细胞系中的研究报告称,具有 6-12 个碳原子的中链脂肪酸(MCFAs)与长链脂肪酸(LCFAs)表现出不同的代谢特性。然而,这些研究报告对不同脂肪酸分子对肝细胞代谢的影响报道并不清楚。本研究旨在捕获 AML12 细胞中辛酸(FA 8:0)、癸酸(FA 10:0)或月桂酸(FA12:0)[LCFA;油酸(FA 18:1)]处理后 MCFA 吸收的代谢动力学,使用 C 标记进行代谢谱分析和动态代谢组分析。用 FA 8:0 或 FA 10:0 处理的细胞培养基中的总酮体浓度分别比用 FA 18:1 处理的高 3.22 倍或 3.69 倍。与 DMSO 处理(对照)相比,FA 12:0 处理并未显著增加酮体水平,而与对照相比,FA 12:0 处理使细胞内三酰基甘油(TG)水平增加了 15.4 倍。FA 12:0 处理的样品的代谢谱与 FA 8:0 处理和 FA 10:0 处理的样品不同,表明 MCFAs 的代谢吸收明显取决于 MCFA 类型。此外,动态代谢组分析清楚地表明,FA 8:0 被快速且定量地氧化为乙酰辅酶 A 并被同化到酮体、柠檬酸循环中间产物和生糖氨基酸中,但不易转化为 TG。