Abstract

Objectives:This study aimed to investigate the mechanisms underlying impaired sperm motility in high-fat diet (HFD)-induced obesity.Methods: Six-week-old male C57BL/6J mice were used to establish an HFD-induced obesity model. Sperm motility and male reproductive function were then evaluated. Macrophage polarization was evaluated by flow cytometry, and key differentially expressed genes were identified by RNA-seq analysis of epididymal adipose tissue, the epididymis, and testes. Finally, pyruvate carboxylase (PC) and the PC inhibitor erianin (Eri) were used to examine the role of adipocyte-derived PC in regulating macrophage polarization.Results: HFD-induced obese mice exhibited abnormal testicular and epididymal morphology, with reduced sperm motility and viability. Flow cytometry revealed that macrophages were polarized toward the M1 phenotype in epididymal adipose tissue and the epididymis in the HFD group. RNA-seq analysis demonstrated thatPCwas the most significantly upregulated gene in epididymal adipose tissue. Furthermore,PCexpression increased during adipocyte maturation in vitro. Mature adipocytes promoted macrophage polarization toward the M1 phenotype, while Eri attenuated this effect. In addition, supernatants from LPS-induced M1 macrophages contained elevated levels of inflammatory cytokines and significantly reduced sperm motility and viability.Conclusions: HFD-induced obesity impaired sperm quality and male reproductive function. The underlying mechanism may involve increased PC expression, which drives epididymal macrophages toward M1 polarization and triggers local chronic inflammation, ultimately compromising sperm motility and viability.