Monocarboxylate transporter 4 deficiency enhances high-intensity interval training-induced metabolic adaptations in skeletal muscle

被引:2
|
作者
Tamura, Yuki [1 ,2 ,3 ,4 ,5 ,6 ,9 ]
Jee, Eunbin [2 ]
Kouzaki, Karina [3 ,7 ,8 ]
Kotani, Takaya [3 ]
Nakazato, Koichi [2 ,3 ,7 ,8 ]
机构
[1] Nippon Sport Sci Univ, Fac Sport Sci, Tokyo, Japan
[2] Nippon Sport Sci Univ, Grad Sch Hlth & Sport Sci, Tokyo, Japan
[3] Nippon Sport Sci Univ, Res Inst Sport Sci, Tokyo, Japan
[4] Nippon Sport Sci Univ, Sport Training Ctr, Tokyo, Japan
[5] Nippon Sport Sci Univ, High Performance Ctr, Tokyo, Japan
[6] Nippon Sport Sci Univ, Ctr Coaching Excellence, Tokyo, Japan
[7] Nippon Sport Sci Univ, Fac Med Sci, Tokyo, Japan
[8] Nippon Sport Sci Univ, Grad Sch Med & Hlth Sci, Tokyo, Japan
[9] Nippon Sport Sci Univ, 7-1-1 Fukasawa,Setagaya, Tokyo 1588508, Japan
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2024年 / 602卷 / 07期
基金
日本学术振兴会;
关键词
exercise; glycolysis; high-intensity interval training; lactate; metabolism; mitochondria; monocarboxylate transporter; skeletal muscle; LACTATE SHUTTLE; EXERCISE; DEHYDROGENASE; MCT1; EXPRESSION; ACTIVATION; BIOGENESIS; PYRUVATE; NETWORK; BRAIN;
D O I
10.1113/JP285719
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
High-intensity exercise stimulates glycolysis, subsequently leading to elevated lactate production within skeletal muscle. While lactate produced within the muscle is predominantly released into the circulation via the monocarboxylate transporter 4 (MCT4), recent research underscores lactate's function as an intercellular and intertissue signalling molecule. However, its specific intracellular roles within muscle cells remains less defined. In this study, our objective was to elucidate the effects of increased intramuscular lactate accumulation on skeletal muscle adaptation to training. To achieve this, we developed MCT4 knockout mice and confirmed that a lack of MCT4 indeed results in pronounced lactate accumulation in skeletal muscle during high-intensity exercise. A key finding was the significant enhancement in endurance exercise capacity at high intensities when MCT4 deficiency was paired with high-intensity interval training (HIIT). Furthermore, metabolic adaptations supportive of this enhanced exercise capacity were evident with the combination of MCT4 deficiency and HIIT. Specifically, we observed a substantial uptick in the activity of glycolytic enzymes, notably hexokinase, glycogen phosphorylase and pyruvate kinase. The mitochondria also exhibited heightened pyruvate oxidation capabilities, as evidenced by an increase in oxygen consumption when pyruvate served as the substrate. This mitochondrial adaptation was further substantiated by elevated pyruvate dehydrogenase activity, increased activity of isocitrate dehydrogenase - the rate-limiting enzyme in the TCA cycle - and enhanced function of cytochrome c oxidase, pivotal to the electron transport chain. Our findings provide new insights into the physiological consequences of lactate accumulation in skeletal muscle during high-intensity exercises, deepening our grasp of the molecular intricacies underpinning exercise adaptation.
引用
收藏
页码:1313 / 1340
页数:28
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