Nieman David C, Sakaguchi Camila A, Williams James C, Lawson Jackie, Lambirth Kevin C
Human Performance Laboratory, Appalachian State University, North Carolina Research Campus, Kannapolis, NC 28081, USA.
College of Computing and Informatics, University of North Carolina at Charlotte, Kannapolis, NC 28081, USA.
Nutrients. 2025 Aug 26;17(17):2765. doi: 10.3390/nu17172765.
BACKGROUND/OBJECTIVES: This study examined the effects of 2 weeks of betaine versus placebo supplementation (3 g/d) on 60 km cycling performance, gut permeability, and shifts in plasma metabolites.
Participants included 21 male and female non-elite cyclists. A randomized, placebo-controlled, double-blind, crossover design was used with two 2-week supplementation periods and a 2-week washout period. Supplementation periods were followed by a 60 km cycling time trial. Six blood samples were collected before and after supplementation (overnight fasted state), and at 0 h, 1.5 h, 3 h, and 24 h post-exercise. Five-hour urine samples were collected pre-supplementation and post-60 km cycling after ingesting a sugar solution containing lactulose 5 g, C mannitol 100 mg, and C mannitol 1.9 g in 450 mL water. Other outcome measures included plasma intestinal fatty acid binding protein-1 (I-FABP), muscle damage biomarkers (serum creatine kinase, myoglobin), serum cortisol, complete blood cell counts, and shifts in plasma metabolites using untargeted metabolomics.
The time to complete the 60 km cycling bout differed significantly between the betaine and placebo trials (mean ± SE, 112.8 ± 2.3, 114.2 ± 2.6 min, respectively, (-1.41 ± 0.7 min) (effect size = 0.475, = 0.042). No trial differences were found for I-FABP (interaction effect, = 0.076), L:CM ( = 0.559), the neutrophil/lymphocyte ratio ( = 0.171), serum cortisol ( = 0.982), serum myoglobin ( = 0.942), or serum creatine kinase ( = 0.694). Untargeted metabolomics showed that 214 metabolites exhibited significant trial treatment effects and 130 significant trial x time interaction effects. Betaine versus placebo supplementation was linked to significant increases in plasma betaine, dimethylglycine (DMG), sarcosine, methionine, S-adenosylhomocysteine (SAH), alpha-ketoglutaramate, and 5'methylthioadensone (MTA), and decreases in plasma carnitine and numerous acylcarnitines.
Betaine supplementation modestly improved 60 km cycling performance but had no effect on gut permeability. The metabolomics data supported a strong influence of 2-week intake of betaine on the one-carbon metabolism pathway during the 24 h recovery period.
背景/目的:本研究探讨了连续2周补充甜菜碱(3克/天)与补充安慰剂对60公里骑行表现、肠道通透性以及血浆代谢物变化的影响。
参与者包括21名非精英男女自行车运动员。采用随机、安慰剂对照、双盲、交叉设计,包括两个为期2周的补充期和一个2周的洗脱期。补充期后进行60公里的骑行计时赛。在补充前后(过夜禁食状态)以及运动后0小时、1.5小时、3小时和24小时采集六份血样。在补充前以及在摄入含有5克乳果糖、100毫克C-甘露醇和1.9克C-甘露醇的450毫升糖水后进行60公里骑行后,收集5小时尿液样本。其他结果指标包括血浆肠脂肪酸结合蛋白-1(I-FABP)、肌肉损伤生物标志物(血清肌酸激酶、肌红蛋白)、血清皮质醇、全血细胞计数,以及使用非靶向代谢组学分析血浆代谢物的变化。
甜菜碱组和安慰剂组完成60公里骑行的时间存在显著差异(平均值±标准误,分别为112.8±2.3、114.2±2.6分钟,差值为(-1.41±0.7分钟)(效应量=0.475,P=0.042)。在I-FABP(交互效应,P=0.076)、L:CM(P=0.559)、中性粒细胞/淋巴细胞比值(P=0.171)、血清皮质醇(P=0.982)、血清肌红蛋白(P=0.942)或血清肌酸激酶(P=0.694)方面未发现试验组间差异。非靶向代谢组学显示,214种代谢物表现出显著的试验处理效应,130种表现出显著的试验×时间交互效应。与补充安慰剂相比,补充甜菜碱导致血浆甜菜碱、二甲基甘氨酸(DMG)、肌氨酸、蛋氨酸、S-腺苷同型半胱氨酸(SAH)、α-酮戊二酸和5'-甲硫基腺苷(MTA)显著增加,血浆肉碱和多种酰基肉碱减少。
补充甜菜碱适度改善了60公里骑行表现,但对肠道通透性无影响。代谢组学数据支持在24小时恢复期内,连续2周摄入甜菜碱对一碳代谢途径有强烈影响。