Effect of extenders and sperm concentration on migration efficiency of Malabari buck spermatozoa in bovine cervical mucus

The study evaluated the effect of extenders and sperm concentration on the migration efficiency of Malabari buck spermatozoa in bovine cervical mucus. Fresh semen ejaculates collected on six different days from three adult healthy Malabari bucks were pooled and divided into four groups based on the extender used (tris-egg yolk-based or liposome-based extender) and rate of extension (200 or 400 million motile spermatozoa per 0.5 mL) (n=6 per group) and subjected to cryopreservation. After freezing and thawing, Malabari buck spermatozoa cryopreserved in liposome-based extender travelled significantly (p<0.05) greater distance in bovine cervical mucus compared to those preserved in tris-egg yolk-based extender when packed in French medium straws with 200 million progressively motile spermatozoa. The corresponding values with 400 million progressively motile spermatozoa also showed the same trend. It was also observed that Malabari buck semen extended with 200 million progressively motile spermatozoa was significantly (p<0.05) better in terms of migration efficiency in bovine cervical mucus compared to that with 400 million progressively motile spermatozoa in both the extenders

Effect of cholesterol supplementation on cryosurvival of goat spermatozoa

Aim: Sperm membrane cholesterol influences cryodamage during cryopreservation. The present study was carried out to evaluate the effect of varying cholesterol levels in Tris based extenders on the freezability of sexually healthy Malabari buck semen. Materials and Methods: A total of 48 ejaculates from two adults healthy sexually healthy Malabari bucks were utilized for the study. The collected and pooled ejaculates were divided into four groups with Group I serving as Control - I, Group II and III were treated with 1 mg and 2 mg of cholesterol-loaded-cyclodextrin (CLC)/120 × 106 spermatozoa, respectively, and Group IV treated with 1 mg methyl-β-cyclodextrin (MβCD) served as Control - II. Manual freezing was carried out to cryopreserve the treated and control spermatozoa. Results: Treatment of semen samples with CLC resulted in improved maintenance of sperm motility at pre-freeze and post-thaw stages of cryopreservation without affecting hypo-osmotic swelling response. Treatment of semen with 1 mg of CLC/120 × 106 spermatozoa was observed to be better than treatment with 2 mg of CLC/120 × 106 spermatozoa. In general, MβCD treatment was found to result in significantly lower sperm characteristics than those of Control - I and CLC treatment at pre-feeze and post-thaw stages and when incubated up to 4 h. Conclusion: Cholesterol treatment of sexually healthy Malabari buck semen was found to hold promise for improving cryopreser-vability of spermatozoa