Skeletal muscle PGC-1?1 reroutes kynurenine metabolism to increase energy efficiency and fatigue-resistance.

ABSTRACT: The coactivator PGC-1?1 is activated by exercise training in skeletal muscle and promotes fatigue-resistance. In exercised muscle, PGC-1?1 enhances the expression of kynurenine aminotransferases (Kats), which convert kynurenine into kynurenic acid. This reduces kynurenine-associated neurotoxicity and generates glutamate as a byproduct. Here, we show that PGC-1?1 elevates aspartate and glutamate levels and increases the expression of glycolysis and malate-aspartate shuttle (MAS) genes. These interconnected processes improve energy utilization and transfer fuel-derived electrons to mitochondrial respiration. This PGC-1?1-dependent mechanism allows trained muscle to use kynurenine metabolism to increase the bioenergetic efficiency of glucose oxidation. Kat inhibition with carbidopa impairs aspartate biosynthesis, mitochondrial respiration, and reduces exercise performance and muscle force in mice. Our findings show that PGC-1?1 activates the MAS in skeletal muscle, supported by kynurenine catabolism, as part of the adaptations to endurance exercise. This crosstalk between kynurenine metabolism and the MAS may have important physiological and clinical implications.

SUBMITTER: Agudelo LZ 

PROVIDER: S-EPMC6591322 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature