Cooling of equine semen at 16°C for 36 hours with addition of different glutathione concentrations

Handling equine semen during the refrigeration process reduces sperm viability, and consequently causes membrane lipid peroxidation, among other challenges. The present study aimed to evaluate the in vitro effects of glutathione (control, 1. 0, 1. 5, and 2. 5 mM) on equine semen in a cooled protocol of 16 degrees C for 36 hours. The following variables were evaluated after 0, 12, 24, and 36 hours refrigeration: total sperm motility, vigor, viability, and plasma and acrosomal membrane integrity. Motility was higher with 2. 5mM of glutathione (57. 8 +/- 7. 3) after 12 hours of refrigeration compared to the control (53. 2 +/- 8. 3) (P < 0. 05). After 36 hours of refrigeration, motility was higher with 1. 5 mM (43. 4 +/- 12. 7) and 2. 5mM glutathione (45. 5 +/- 6. 2), than it was with 1mM glutathione (38. 2 +/- 9) and the control (35. 5 +/- 18. 4) (P < 0. 05), respectively. The strength was highest with 1. 5mM glutathione (3. 7 +/- 0. 3) after 36 hours compared to the control (3. 2 +/- 1. 1), (P < 0. 05). Viability differed between control and 1mM treatments (79. 5 +/- 1. 8) only after 24 hours (75. 5 +/- 9. 7) (P < 0. 05). Throughout the investigation, no significant differences were noted in plasma and acrosomal membrane integrity (P > 0. 05). The 1. 5 and 2. 5mM glutathione levels were more efficient in protecting sperm cells and yielded higher total motility values after 36 hours of refrigeration.