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Storing fresh equine semen
Bovine semen frozen in egg yolk
Five different vitrification devices
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Post-thaw viability of dog semen
Cushioned centrifugation technique
Post-thaw sperm parameters in ram semen
Fertility of ram semen frozen in Bioxcell
Fecundity of stored porcine semen
Improved viability following a storage period
Boar semen quality
Motility of porcine spermatozoa
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Storing fresh equine semen

  • Batellier, F., Duchamp, G., Vidament, M., Arnaud, G., Palmer, E., and Magistrini, M.
  • Delayed insemination is successful with a new extender for storing fresh equine semen at 15 degrees C under aerobic conditions.
  • Theriogenology. 50, 229-236.
  • 1998
  • Ref ID: BATELLIER1998

Abstract: Milk-based semen diluents are known to be practical and effective in protecting equine spermatozoa during storage before artificial insemination. Milk is a biological fluid with a complex composition and contains components which are beneficial or harmful to spermatozoa. The aim of this study was to test the fertility of stallion semen after long-term storage using different milk diluents (INRA 82 or Kenney's diluent) vs one diluent chemically defined (INRA 96), which is composed of efficient milk components and optimized for sperm survival and storage temperature. The milk fraction used was that which best maintained spermatozoal survival based on motility measured in previous studies. Four breeding trials were conducted to determine the influence of combination of new diluent and storage conditions on fertility of the stallion. We compared the standard protocol of storing semen in a skim milk diluent (INRA 82 or Kenney's diluent) at 4 degrees C under anaerobic conditions with the experimental protocol which consisted of storing in a chemically defined, milk-free diluent (INRA 96), at 15 degrees C, under aerobic conditions. After 4 breeding trials, in which the semen was stored for 24 h under the 2 protocols, we obtained 57% (n = 178) and 40% (n = 173) of fertility per cycle using the experimental and the standard protocol respectively (p < 0.001). Another breeding trial was conducted to determine the influence of storage time on the fertility of spermatozoa. We have compared the fertility of semen inseminated immediately (68% of fertility per cycle, n = 50) vs the fertility of semen stored under the experimental protocol for 72 h before insemination (48% of fertility per cycle, n = 52). The experimental protocol improved sperm fertility compared to the standard protocol and seems to be a particular alternative for stallions with cold shock sensitive spermatozoa. Storing semen for 72 h under the experimental protocol seems to be useful in the field