Research progress on exercise-induced macrophage trained immune tolerance in improving insulin resistance

By modulating the tolerance of innate immune cells to TI and blocking the pathological cycle between IR and TI, it is possible to alleviate chronic inflammation caused by metabolism abnormalities secondary to IR, providing a new targeted intervention point for preventing and treating insulin resistance. Numerous studies have shown that exercise can alter macrophage metabolism, thereby changing their polarization phenotype to improve overall metabolism and alleviate chronic inflammation.

Exercise promotes metabolic reprogramming in macrophages through oxidative phosphorylation and mitochondrial fatty acid oxidation, which induces trained immunity tolerance and drives macrophages toward an anti-inflammatory M2 phenotype. At the same time, cellular energy metabolism is enhanced, glucose uptake and mitochondrial function are improved, and reactive oxygen species clearance is increased. These changes collectively promote the conversion of immune cells to an anti-inflammatory phenotype and inhibit pro-inflammatory expression, thereby reducing systemic inflammation and improving IR.