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ANIMAL GROWTH, PHYSIOLOGY, AND REPRODUCTION |
Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins 80523
2 Correspondence: ARBL Bldg., Foothills Campus (phone: 970-491-8409; fax: 970-491-3557; e-mail: esquires{at}colostate.edu).
Abstract
The ability to ship cooled stallion sperm for subsequent freezing at a facility specializing in cryopreservation would be beneficial to the equine industry. Stallion sperm has been centrifuged, cooled to 5°C for 12 h, and frozen without a detrimental effect on motility in a previous study; however, no fertility data were available. Experiment 1 compared the post-thaw motility of sperm cooled for 18 h at 15 or 5°C at either 400 or 200 x 106 sperm/mL and then frozen. Storage temperature, sperm concentration, or the interaction of temperature and concentration had no effect on total (TM) and progressive motility (PM) after cooling. Post-thaw TM and PM were higher for control than (P < 0.05) for treated samples. There was no difference in post-thaw TM and PM due to temperature or concentration. Experiment 2 further evaluated procedures for cooling before freezing. Ejaculates were either cooled to 5°C for 18 h and centrifuged, centrifuged at room temperature and then cooled to 5°C for 18 h before freezing, or centrifuged and frozen immediately (control). There was no difference among treatments on post-thaw TM or PM. In Exp. 3, mares were inseminated with semen that had been extended in skim milk-egg yolk without glycerol, centrifuged, resuspended at 200 x 106 sperm/mL, cooled to 5°C for 18 h, and then frozen or not cooled for 18 h before freezing (control). Pregnancy rates did not differ for mares receiving semen cooled and then frozen (21 of 30, 70%) or semen frozen directly without prior cooling (16 of 30, 53%). In summary, a procedure was developed for cooling stallion sperm for 18 h before freezing without a resultant decrease in fertility.
Key Words: Cooling Fertility Freezing Stallion Sperm Storage
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