Nutrition Research Institute, University of North Carolina at Chapel Hill, Kannapolis, North Carolina.
Department of Biochemistry & Molecular Biology, Hollings Cancer center, Medical University of South Carolina, 173 Ashley Avenue, Charleston, South Carolina.
J Nutr Biochem. 2021 Dec;98:108832. doi: 10.1016/j.jnutbio.2021.108832. Epub 2021 Aug 4.
Folic acid-fortified foods and multi-vitamin supplements containing folic acid (FA) are widely used around the world, but the exact mechanisms/metabolic effects of FA are not precisely identified. We have demonstrated that Ceramide Synthase 6 (CerS6) and C-ceramide mediate response to folate stress in cultured cells. Here we investigated the dietary FA effects on mouse liver metabolome, with a specific focus on sphingolipids, CerS6 and C-ceramide. Wild-type and CerS6 mice were fed FA-deficient, control, or FA over-supplemented diets for 4 weeks. After dietary treatment, liver concentrations of ceramides, sphingomyelins and hexosylceramides were measured by LC-MS/MS and complemented by untargeted metabolomic characterization of mouse livers. Our study shows that alterations in dietary FA elicit multiple sphingolipid responses mediated by CerS6 in mouse livers. Folic acid-deficient diet elevated C-, C- and C- but not C-ceramide in WT male and female mice. Additionally, FA over-supplementation increased multiple sphingomyelin species, including total sphingomyelins, in both sexes. Of note, concentrations of C- and C-ceramides and hexosylceramides were significantly higher in female livers than in male. The latter were increased by FD diet, with no difference between sexes in total pools of these sphingolipid classes. Untargeted liver metabolomic analysis concurred with the targeted measurements and showed broad effects of dietary FA and CerS6 status on multiple lipid classes including sex-specific effects on phosphatidylethanolamines and diacylglycerols. Our study demonstrates that both dietary FA and CerS6 status exhibit pleiotropic and sex-dependent effects on liver metabolism, including hepatic sphingolipids, diacylglycerols, long chain fatty acids, and phospholipids.
叶酸强化食品和含有叶酸(FA)的多种维生素补充剂在世界范围内广泛使用,但 FA 的确切机制/代谢作用尚不清楚。我们已经证明 Ceramide Synthase 6(CerS6)和 C-ceramide 介导了培养细胞中叶酸应激的反应。在这里,我们研究了饮食 FA 对小鼠肝脏代谢组的影响,特别关注鞘脂,CerS6 和 C-ceramide。野生型和 CerS6 小鼠分别用 FA 缺乏、对照或 FA 过度补充饮食喂养 4 周。在饮食处理后,通过 LC-MS/MS 测量肝脏中的 ceramides、sphingomyelins 和 hexosylceramides 的浓度,并通过对小鼠肝脏的非靶向代谢组学特征进行补充。我们的研究表明,饮食 FA 的改变会引起 CerS6 介导的小鼠肝脏中多种鞘脂反应。叶酸缺乏饮食会增加 WT 雌雄小鼠的 C-、C-和 C-但不是 C-ceramide。此外,FA 过度补充会增加多种鞘磷脂种类,包括总鞘磷脂,在两性中均有增加。值得注意的是,C-和 C-ceramide 和 hexosylceramides 的浓度在雌性肝脏中明显高于雄性。后者在 FD 饮食中增加,两性鞘脂类总池无差异。非靶向肝脏代谢组学分析与靶向测量结果一致,并显示饮食 FA 和 CerS6 状态对多种脂质类别的广泛影响,包括对磷脂酰乙醇胺和二酰基甘油的性别特异性影响。我们的研究表明,饮食 FA 和 CerS6 状态都对肝脏代谢表现出多效性和性别依赖性影响,包括肝脏鞘脂、二酰基甘油、长链脂肪酸和磷脂。