The preservation of rooster semen quality during short-term liquid storage remains a challenge in poultry reproductive biotechnology because sperm cells rapidly lose functional competence under ambient conditions. This deterioration is largely associated with oxidative stress and lipid peroxidation of sperm membranes, which are particularly vulnerable in avian species due to their high polyunsaturated fatty acid content and limited cytoplasmic antioxidant defenses. Selenium is an essential trace element involved in cellular antioxidant protection through its incorporation into several selenoproteins that regulate redox balance and protect cellular structures from oxidative injury. The present study evaluated the effects of selenium methionine supplementation on rooster semen quality during liquid storage at 25 °C. Semen was diluted using a standard poultry semen extender composed of sodium glutamate, glucose, potassium acetate, magnesium acetate, and potassium citrate. Selenium methionine was incorporated into the semen extender at concentrations of 0.5%, 1%, and 2% (w/v) at the time of semen dilution prior to storage. Semen quality was assessed at 0, 4, 8, 12, and 24 h of storage. Functional parameters, including total sperm motility, sperm viability, and dead sperm percentage, together with kinematic variables (VSL, VCL, VAP, ALH, LIN, and STR), were analyzed using computer-assisted sperm analysis (CASA). Structural integrity was evaluated through acrosome and plasma membrane integrity tests, while sperm physiological status and apoptotic progression were assessed using Annexin V-FITC/propidium iodide flow cytometry. Significant effects of storage time, selenium methionine concentration, and their interaction were observed for multiple semen quality parameters (p < 0.05). Among the tested concentrations, supplementation with 0.5% selenium methionine consistently produced the most favorable results, maintaining higher sperm motility, viability, and membrane integrity while reducing dead sperm percentage and apoptotic progression during storage, with protective effects particularly evident at 8, 12, and 24 h compared with the control and higher concentrations. Polynomial contrast analysis indicated predominantly non-linear dose–response relationships, with quadratic and cubic components providing the best model fit (R2 = 0.90–0.99; p < 0.0001), suggesting a hormetic antioxidant effect. Overall, these findings indicate that selenium methionine supplementation in semen extender improves the stability of rooster semen during short-term liquid storage at ambient temperature, with 0.5% showing the most consistent protective effects among the concentrations evaluated.
Arif et al. (Mon,) studied this question.