Quattrone Alda, Fehri Nour Elhouda, Agradi Stella, Menchetti Laura, Barbato Olimpia, Castrica Marta, Sulçe Majlind, Castellini Cesare, Muça Gerald, Mattioli Simona, Vigo Daniele, Migni Giovanni, Nompleggio Lorenzo, Belabbas Rafik, Gualazzi Fabio, Ricci Giovanni, Postoli Rezart, Di Federico Francesca, Moretti Elena, Zalla Pellumb, Collodel Giulia, Brecchia Gabriele, Curone Giulio
Department of Veterinary Medicine and Animal Sciences, University of Milan, Via dell'Università 6, 26900 Lodi, Italy.
Department of Veterinary Sciences, University of Torino, Largo Paolo Braccini 2, 10095 Grugliasco, Italy.
Antioxidants (Basel). 2025 Apr 2;14(4):431. doi: 10.3390/antiox14040431.
Lipopolysaccharide (LPS)-induced inflammation impairs sperm function; however, its impact on ejaculated rabbit sperm remains unexplored. This dose-response study aims to determine the LPS concentration that negatively affects sperm motility in vitro, while also providing the first identification of TLR4 localization on rabbit spermatozoa. Additionally, it evaluates malondialdehyde (MDA) levels in seminal plasma as an indicator of oxidative stress. Sperm motility was analyzed using computer-assisted sperm analysis (CASA) after incubation with increasing LPS concentrations (0, 50, 100, 200, 400, 600, and 800 µg/mL) at multiple time points (0, 1, 2, and 4 h). LPS doses ≥ 400 µg/mL significantly reduced progressive and non-progressive motility, as well as curvilinear velocity (all < 0.001), while increasing the proportion of static spermatozoa ( < 0.05). Receiver operating characteristic (ROC) analysis identified 300 µg/mL as the threshold dose for motility decline. Immunofluorescence revealed TLR4 localization in the midpiece of sperm tails, with weak labeling in control samples and a marked increase after 4 h of incubation with 400 μg/mL LPS. MDA levels were assessed using the thiobarbituric acid reactive substances (TBARS) assay with a colorimetric kit, showing no significant effect of LPS treatment. No correlation was found between MDA and other semen parameters. ccThese findings identify TLR4 on rabbit sperm for the first time and establish a threshold LPS dose for future in vitro studies.
脂多糖(LPS)诱导的炎症会损害精子功能;然而,其对射出的兔精子的影响尚未得到探索。这项剂量反应研究旨在确定体外对精子活力产生负面影响的LPS浓度,同时首次鉴定兔精子上TLR4的定位。此外,它还评估精浆中丙二醛(MDA)水平作为氧化应激的指标。在多个时间点(0、1、2和4小时)与递增的LPS浓度(0、50、100、200、400、600和800μg/mL)孵育后,使用计算机辅助精子分析(CASA)分析精子活力。LPS剂量≥400μg/mL显著降低了渐进性和非渐进性活力以及曲线速度(均<0.001),同时增加了静止精子的比例(<0.05)。受试者工作特征(ROC)分析确定300μg/mL为活力下降的阈值剂量。免疫荧光显示TLR4定位于精子尾部的中段,对照样品中标记较弱,在与400μg/mL LPS孵育4小时后标记明显增加。使用比色法试剂盒通过硫代巴比妥酸反应性物质(TBARS)测定评估MDA水平,结果显示LPS处理无显著影响。未发现MDA与其他精液参数之间存在相关性。这些发现首次鉴定了兔精子上的TLR4,并确定了未来体外研究的LPS阈值剂量。