Lactate administration induces skeletal muscle synthesis by influencing Akt/mTOR and MuRF1 in non-trained mice but not in trained mice

Physiol Rep. 2024 Feb;12(4):e15952. doi: 10.14814/phy2.15952.

Abstract

The perception regarding lactate has changed over the past decades, and some of its physiological roles have gradually been revealed. However, the effects of exogenous lactate on skeletal muscle synthesis remain unclear. This study aimed to confirm the effects of a 5-week lactate administration and post-exercise lactate administration on skeletal muscle synthesis. Thirty-two Institute of Cancer Research mice were randomly assigned to non-trained + placebo, non-trained + lactate, trained + placebo, and trained + lactate groups. Furthermore, 3 g/kg of lactate or an equivalent volume of saline was immediately administered after exercise training (maximum oxygen uptake: 70%). Lactate administration and/or exercise training was performed 5 days/week for 5 weeks. After the experimental period, it was observed that lactate administration tended to elevate skeletal muscle weight, increased protein kinase B (p < 0.05) and mammalian target of rapamycin (p < 0.05) mRNA levels, and decreased muscle ring-finger protein-1 expression (p < 0.05). Lactate administration after exercise training significantly enhanced plantaris muscle weight; however, it had no additional effects on most signaling factors. This study demonstrated that a 5-week lactate administration could stimulate skeletal muscle synthesis, and lactate administration after exercise training may provide additional effects, such as increasing skeletal muscle.

Keywords: MuRF1; exercise; lactate; mTOR pathway; oral administration; protein synthesis.

MeSH terms

  • Animals
  • Lactic Acid* / metabolism
  • Mammals / metabolism
  • Mice
  • Mice, Inbred Strains
  • Muscle, Skeletal / metabolism
  • Oxygen / metabolism
  • Oxygen Consumption
  • Proto-Oncogene Proteins c-akt* / metabolism
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Lactic Acid
  • Proto-Oncogene Proteins c-akt
  • Oxygen
  • TOR Serine-Threonine Kinases