Kopp Markus, Morisset Rosalie, Rychlik Michael
Chair of Analytical Food Chemistry, Technical University of Munich, Alte Akademie 10, Freising D-85354, Germany.
Institute for Food & Health (Z I E L), Technical University of Munich, Weihenstephaner Berg 1, Freising D-85354, Germany.
Nutrients. 2017 May 5;9(5):462. doi: 10.3390/nu9050462.
Studies on one-carbon metabolism for the assessment of folate deficiency have focused on either metabolites of folate metabolism or methionine cycle. To bridge the gap between deficiency markers in these pathways we designed a dietary induced folate deficiency study using male C57BL/6N mice. After weaning (3 weeks) mice were fed a defined control diet (1 week) before being fed a folate deficient diet ( = 6 mice) and the control diet ( = 6 mice) for 12 additional weeks. Thereafter, we determined total homocysteine in plasma and folate in erythrocytes as well as -adenosylmethionine, -adenosylhomocysteine, and six folate vitamers in tissues including 5-methyltetrahydrofolate, 5-formyltetrahydrofolate, 5,10-methenyltetrahydrofolate, tetrahydrofolate, 10-formylfolic acid, and folic acid by means of stable isotope dilution assays coupled with liquid chromatography tandem mass spectrometry. In all organs, except heart (mainly 5-mehtyltetrahydrofolate), tetrahydrofolate constitutes the main vitamer. Moreover, in liver tetrahydrofolate was most abundant followed by 5-methyltetrahydrofolate (heart: tetrahydrofolate), 5-formyltetrahydrofolate, and 5,10-methenyltetrahydrofolate. Because of the significant decrease ( < 0.05) of folate status and -adenosylmethionine/-adenosylhomocysteine ratio accompanied with increasing -adenosylhomocysteine ( < 0.05), hepatocytes are most susceptible to folate deficiency. To the best of our knowledge, we herein present the first method for simultaneous quantitation of eight metabolites for both folate and methionine cycle in one tissue sample, tHcy in plasma, and erythrocyte folate to shed light on physiological interrelations of one-carbon metabolism.
为评估叶酸缺乏而开展的一碳代谢研究主要聚焦于叶酸代谢的代谢产物或甲硫氨酸循环。为弥合这些途径中缺乏标志物之间的差距,我们设计了一项饮食诱导的叶酸缺乏研究,使用雄性C57BL/6N小鼠。断奶(3周龄)后,小鼠先喂食特定对照饮食1周,然后分别喂食叶酸缺乏饮食(n = 6只小鼠)和对照饮食(n = 6只小鼠)12周。此后,我们通过稳定同位素稀释分析结合液相色谱串联质谱法测定了血浆中的总同型半胱氨酸、红细胞中的叶酸以及组织中的S-腺苷甲硫氨酸、S-腺苷同型半胱氨酸和六种叶酸维生素,包括5-甲基四氢叶酸、5-甲酰基四氢叶酸、5,10-亚甲基四氢叶酸、四氢叶酸、10-甲酰叶酸和叶酸。在所有器官中,除心脏(主要是5-甲基四氢叶酸)外,四氢叶酸是主要的维生素形式。此外,肝脏中四氢叶酸含量最丰富,其次是5-甲基四氢叶酸(心脏:四氢叶酸)、5-甲酰基四氢叶酸和5,10-亚甲基四氢叶酸。由于叶酸状态和S-腺苷甲硫氨酸/S-腺苷同型半胱氨酸比值显著降低(P < 0.05),同时S-腺苷同型半胱氨酸增加(P < 0.05),肝细胞对叶酸缺乏最为敏感。据我们所知,我们在此提出了一种在一个组织样本中同时定量叶酸和甲硫氨酸循环的八种代谢产物、血浆中的总同型半胱氨酸和红细胞叶酸的方法,以阐明一碳代谢的生理相互关系。