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

• Published in: The Journal of physiology 2024-04, Vol.602 (7), p.1313-1340
• Main Authors: Tamura, Yuki, Jee, Eunbin, Kouzaki, Karina, Kotani, Takaya, Nakazato, Koichi
• Format: Article
• Language: English
• Subjects: Adaptation; Animals; Cytochrome-c oxidase; Dehydrogenases; Electron transport chain; Enzymatic activity; Enzymes; exercise; Glycogen; Glycogen phosphorylase; Glycolysis; Hexokinase; High-Intensity Interval Training; Interval training; Intracellular signalling; Isocitrate dehydrogenase; Kinases; lactate; Lactates; Lactic acid; Metabolism; Mice; Mice, Inbred ICR; Mice, Knockout; Mitochondria; monocarboxylate transporter; Muscle contraction; Muscle, Skeletal - physiology; Musculoskeletal system; Oxygen consumption; Phosphorylase; Physical training; Pyruvate kinase; Pyruvates - metabolism; Pyruvic acid; Skeletal muscle; Tricarboxylic acid cycle
• ISSN: 0022-3751; 1469-7793
• DOI: 10.1113/JP285719

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. Key points We pioneered a unique line of monocarboxylate transporter 4 (MCT4) knockout mice specifically tailored to the ICR strain, an optimal background for high‐intensity exercise studies. A deficiency in MCT4 exacerbates the accumulation of lactate in skeletal muscle during high‐intensity exercise. Pairing MCT4 deficiency with high‐intensity interval training (HIIT) results in a synergistic boost in high‐intensity exercise capacity, observable both at the organismal level (via a treadmill running test) and at the muscle tissue level (through an ex vivo muscle contrac