Collodel Giulia, Moretti Elena, Marcucci Caterina, Liguori Laura, Marchini Daniela, Corsaro Roberta, Centini Gabriele, Signorini Cinzia
Department of Molecular and Developmental Medicine, University of Siena, 53100 Siena, Italy.
Department of Life Sciences, University of Siena, 53100 Siena, Italy.
Biology (Basel). 2025 Jan 28;14(2):137. doi: 10.3390/biology14020137.
Peroxisome Proliferator-Activated Receptor Gamma (PPARγ) is a regulating agent in antioxidant response also involved in controlling inflammation. The impact of varicocele and urogenital infections on sperm PPARγ expression was studied. The PPARγ gene expression was investigated in spermatozoa of 26 normozoospermic men grouped according to their clinical conditions: normal semen parameters (N), normal semen parameters and varicocele (N + V), and normal semen parameters and urogenital infections (N + UI). Sperm PPARγ expression was correlated with F-isoprostanes (F-IsoPs), as markers of lipid peroxidation, and Resolvin D1 (RvD1), a pro-resolving mediator in inflammation. Sperm PPARγ expression was evaluated through comparative real-time PCR, and F-IsoPs and RvD1 were quantified in the seminal plasma via GC/NCI-MS/MS and immunoassay, respectively. PPARγ expression correlates positively with sperm morphology and vitality and negatively with F-IsoPs and RvD1. Sperm morphology positively correlates with vitality and negatively with F-IsoP and RvD1 levels. Despite the normozoospermia in the three examined groups, sperm morphology and PPARγ expression were significantly reduced in N + V and N + UI groups compared to the N group. Additionally, F-IsoP and RvD1 levels were elevated in N + V and N + UI patients. These data suggest that PPARγ expression is compromised by inflammation and lipoperoxidation, providing new insights to further explore new possibilities of targeted treatment of male infertility.
过氧化物酶体增殖物激活受体γ(PPARγ)是抗氧化反应中的一种调节因子,也参与炎症控制。研究了精索静脉曲张和泌尿生殖系统感染对精子PPARγ表达的影响。在26名正常精子症男性的精子中研究了PPARγ基因表达,这些男性根据临床情况分组:精液参数正常(N)、精液参数正常且患有精索静脉曲张(N + V)、精液参数正常且患有泌尿生殖系统感染(N + UI)。精子PPARγ表达与作为脂质过氧化标志物的F-异前列腺素(F-IsoPs)以及炎症中的促消退介质Resolvin D1(RvD1)相关。通过比较实时PCR评估精子PPARγ表达,分别通过气相色谱/负离子化学电离串联质谱法(GC/NCI-MS/MS)和免疫测定法定量精液血浆中的F-IsoPs和RvD1。PPARγ表达与精子形态和活力呈正相关,与F-IsoPs和RvD1呈负相关。精子形态与活力呈正相关,与F-IsoP和RvD1水平呈负相关。尽管三个研究组均为正常精子症,但与N组相比,N + V组和N + UI组的精子形态和PPARγ表达显著降低。此外,N + V组和N + UI组患者的F-IsoP和RvD1水平升高。这些数据表明,PPARγ表达受到炎症和脂质过氧化的损害,为进一步探索男性不育症靶向治疗的新可能性提供了新的见解。