The interactions between monocarboxylate transporter genes MCT1, MCT2, and MCT4 and the kinetics of blood lactate production and removal after high-intensity efforts in elite males: a cross-sectional study.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2025-02-11 DOI:10.1186/s12864-025-11307-4
Ewelina Maculewicz, Andrzej Mastalerz, Aleksandra Garbacz, Anna Mróz, Petr Stastny, Miroslav Petr, Dominik Kolinger, Pavlina Vostatková, Aleksandra Bojarczuk
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Abstract

Background: This cross-sectional study investigated the relationship between genetic variations in monocarboxylate transporter genes and blood lactate production and removal after high-intensity efforts in humans. The study was conducted to explore how genetic variations in the MCT1, MCT2, and MCT4 genes influenced lactate dynamics and to advance the field of sports genetics by pinpointing critical genetic markers that can enhance athletic performance and recovery.

Methods: 337 male athletes from Poland and the Czech Republic underwent two intermittent all-out Wingate tests. Before the tests, DNA samples were taken from each participant, and SNP (single nucleotide polymorphism) analysis was carried out. Two intermittent all-out tests were implemented, and lactate concentrations were assessed before and after these tests.

Results: Sprinters more frequently exhibited the haplotype TAC in the MCT2 gene, which was associated with an increase in the difference between maximum lactate and final lactate concentration. Additionally, this haplotype was linked to higher maximum lactate concentration and was more frequently observed in sprinters. The genotypic interactions AG/T- and GGxT- (MCT1 rs3789592 x MCT4 rs11323780), TTxTT (MCT1 rs12028967 x MCT2 rs3763979), and MCT1 rs7556664 x MCT4 rs11323780 were all associated with an increase in the difference between maximum lactate concentration and final lactate concentration. Conversely, the AGxGG (MCT1 rs3789592 x MCT2 rs995343) interaction was linked to a decrease in this difference. The relationship between maximum lactate concentration and genotypic interactions can be observed as follows: when ATxTT (MCT2 rs3763980 x MCT4 rs11323780) or CTxCT (MCT1 rs10857983 x MCT2 rs3763979) genotypic combinations are present, it leads to a decrease in maximum lactate concentration. Similarly, the combination of CTxCT (MCT1 rs4301628 x MCT2 rs3763979), CT x TT (MCT1 rs4301628 x MCT4 rs11323780), and CTxTT (MCT1 rs4301628 x MCT2 rs3763979) results in decreased maximum lactate concentration.

Conclusions: The TAC haplotype (rs3763980, rs995343, rs3763979) in the MCT2 gene is associated with altered lactate clearance in sprinters, potentially affecting performance and recovery by elevating post-exercise lactate concentrations. While MCT4 rs11323780 is also identified as a significant variant in lactate metabolism, suggesting its role as a biomarker for sprinting performance, further investigation is necessary to clarify underlying mechanisms and consider additional factors. Based on elite male athletes from Poland and the Czech Republic, the study may not generalize to all sprinters or diverse athletic populations. Although genetic variants show promise as biomarkers for sprinting success, athletic performance is influenced by a complex interplay of genetics, environment, and training extending beyond MCT genes.

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单羧酸转运体基因MCT1、MCT2和MCT4与精英雄性高强度运动后血乳酸产生和去除动力学之间的相互作用:一项横断面研究。
背景:本横断面研究调查了人类高强度运动后单羧酸转运体基因的遗传变异与血乳酸产生和去除之间的关系。该研究旨在探索MCT1、MCT2和MCT4基因的遗传变异如何影响乳酸动力学,并通过精确定位可以提高运动表现和恢复的关键遗传标记来推进运动遗传学领域。方法:来自波兰和捷克共和国的337名男性运动员进行了两次间歇性的全面温盖特测试。在测试之前,从每个参与者身上提取DNA样本,并进行SNP(单核苷酸多态性)分析。进行了两次间歇性的全面测试,并在测试前后评估乳酸浓度。结果:短跑运动员更频繁地在MCT2基因中表现出TAC单倍型,这与最大乳酸浓度和最终乳酸浓度之间的差异增加有关。此外,这种单倍型与较高的最大乳酸浓度有关,在短跑运动员中更常见。基因型相互作用AG/T-和GGxT- (MCT1 rs3789592 × MCT4 rs11323780)、TTxTT (MCT1 rs12028967 × MCT2 rs3763979)、MCT1 rs7556664 × MCT4 rs11323780均与最大乳酸浓度和最终乳酸浓度差异增大有关。相反,AGxGG (MCT1 rs3789592 x MCT2 rs995343)相互作用与这种差异的减少有关。最大乳酸浓度与基因型相互作用的关系如下:当ATxTT (MCT2 rs3763980 × MCT4 rs11323780)或CTxCT (MCT1 rs10857983 × MCT2 rs3763979)基因型组合存在时,会导致最大乳酸浓度降低。同样,CTxCT (MCT1 rs4301628 × MCT2 rs3763979)、CT × TT (MCT1 rs4301628 × MCT4 rs11323780)和CTxTT (MCT1 rs4301628 × MCT2 rs3763979)联合使用可降低最大乳酸浓度。结论:MCT2基因中的TAC单倍型(rs3763980、rs995343、rs3763979)与短跑运动员乳酸清除率的改变有关,可能通过提高运动后乳酸浓度影响运动员的表现和恢复。虽然MCT4 rs11323780也被鉴定为乳酸代谢的重要变异,表明其作为短跑成绩的生物标志物的作用,但需要进一步的研究来阐明潜在的机制并考虑其他因素。这项研究基于波兰和捷克共和国的优秀男性运动员,可能不能推广到所有短跑运动员或不同的运动人群。尽管遗传变异显示出作为短跑成功的生物标志物的希望,但运动成绩受到遗传、环境和训练的复杂相互作用的影响,而不仅仅是MCT基因。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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