Fertility of cryopreserved ovine semen is determined by sperm velocity

Fertility of cryopreserved ovine semen is determined by sperm velocity

Del Olmo E, Bisbal A, Maroto-Morales A, García-Alvarez O, Ramon M, Jimenez-Rabadan P, Martínez-Pastor F, Soler AJ, Garde JJ, Fernandez-Santos MR.

SaBio IREC (CSIC – UCLM – JCCM), Campus Universitario s. n. 02071 Albacete, Spain; Regional Center of Animal Selection and Reproduction (CERSYRA) JCCM, 13300 Valdepeñas, Spain; ITRA-ULE, INDEGSAL, University of León, León, Spain; SaBio IREC (CSIC – UCLM – JCCM), Campus Universitario s. n. 02071 Albacete, Spain

The present study aims to examine the predictive value of some sperm parameters on male fertility. Semen samples from six Manchega rams were collected and cryopreserved. Sperm quality was assessed after thawing and after 2h of incubation, either in the freezing extender (37°C) or after dilution in Synthetic Oviductal Fluid (SOF) (38°C, 5% CO2), attempting to mimic the physiological conditions of the female reproductive tract. The following sperm parameters were evaluated: motility and kinetic parameters by computer-assisted semen analyzer (CASA), and sperm viability (propidium iodide), mitochondrial membrane potential (JC-1), apoptotic-like membrane changes (YO-PRO-1), acrosomal status (PNA-FITC), and intracellular calcium (fluo-3) by flow cytometry. Results showed no significant differences between incubation media neither after thawing nor after incubation. There were no significant correlations between fertility and sperm parameters assessed by flow cytometry. However, after incubation in the freezing extender, sperm samples from males with poor fertility yielded less linearity and velocity (P<0.05) as indicated by motility parameters analyzed by CASA. These results indicate that kinematic sperm motility parameters evaluation by CASA might be useful to identify samples with poor fertility.

doi:10.1016/j.anireprosci.2013.02.007