Abstract

To explore the effect of silymarin on bull spermatozoa during cooling and cryopreservation. Semen was collected by artificial vagina from Holstein bulls born in Iraq and diluted by Tris-Citrate-Fructose egg yolk diluents. Diluted spermatozoa were treated with silymarin (0.018 mg/50ml, 0.027 mg/50ml, 0.036 mg/50ml), and packaged in 0.25 ml straws, which were further cooled to 5°C before freezing in liquid nitrogen. Thawing was carried out at 37°C for 30 sec, and the progressive motility%, dead%, abnormality% and acrosome integrity% were assessed, concentrations of addition to the control (0.0 mg/ml) reaching a final volume of 10 ml in each tube. The results proved after cooling and freezing, Individual motility% of sperm was significantly (p< 0.05) higher in T1 which differed significantly (p< 0.05) from T2 and T3 and all these values significantly (p< 0.05) different from control mean while values of dead sperm% show the lowest in T1 which is significantly (p< 0.05) different from control after cooling while after freezing lowest value in T1 and T2 and highest in T3 and control with significant (p<0.05) different. Abnormal sperm% was lowest in T1 after cooling with significant different(p< 0.05) from T2, T3 and control.

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