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Journal of equine veterinary science2019; 85; 102819; doi: 10.1016/j.jevs.2019.102819

Stallion Sperm Integrity After Centrifugation to Reduce Seminal Plasma Concentration and Cool Storage for 4 days.

Abstract: The objective of the study was to investigate if reducing the seminal plasma of stallion extended semen by centrifugation once will suffice to maintain acceptable semen quality for insemination after 4 days of cool storage. Collected semen was extended to 25 × 106 sperm/mL and subjected to one of the following treatments: noncentrifuged (control), centrifuged for 10 minutes at 900 × g and 1800 × g. The supernatant was partially removed, and the sperm pellet, reconstituted and re-extended. It was then placed in a passive cooling device overnight and then transferred to a refrigerator for the remainder of the cooling period. At day 0, 2, and 4, total motility (TM), progressive motility (PM), and plasma (PLM) and acrosomal membrane integrity were assessed. Centrifuged groups had higher TM and PM at day 4 than the control group (P < .05). Likewise, centrifuged groups had higher intact PLM in day 4 (P < .05). A single centrifugation cycle to reduce seminal plasma concentration will suffice to preserve sperm integrity acceptable for an artificial insemination dose up to 4 days of cool storage.
Publication Date: 2019-11-04 PubMed ID: 31952647DOI: 10.1016/j.jevs.2019.102819Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research seeks to understand if a single cycle of centrifugation can effectively maintain the quality of stallion extended semen stored under cool conditions for up to 4 days. The results indicate that a single centrifugation cycle indeed preserves sperm integrity for up to 4 days of storage, showing better motility and plasma and acrosomal membrane integrity compared to non-centrifuged control group.

Research Methodology

  • The study started by extending the collected semen to 25 x 10 sperm/mL. The extended semen was then classified into three groups: the control group which was not centrifuged, a group centrifuged for 10 minutes at 900 x g, and a third group centrifuged for 10 minutes at 1800 x g.
  • The researchers partially removed the supernatant (the liquid lying above a solid residue after crystallization, precipitation, sedimentation, or centrifugation). After this, the remaining sperm pellet was reconstituted and extended once more.
  • The resuspended semen was placed in a passive cooling device overnight and then transferred to a refrigerator for the remainder of the cooling period.

Research Results

  • At day 0, 2, and 4, total motility (TM), progressive motility (PM), and plasma (PLM) and acrosomal membrane integrity of the sperm were assessed.
  • The research showed that the centrifuged groups maintained higher TM and PM at day 4 compared to the control group (P < .05). Likewise, centrifuged groups had higher intact PLM on day 4 (P < .05).
  • These results suggest that a single centrifugation cycle to reduce seminal plasma concentration is sufficient to preserve sperm integrity acceptable for artificial insemination up to 4 days of cool storage.

Research Conclusions

  • The findings provide useful insight for professionals in animal reproduction and artificial insemination, demonstrating that a single centrifugation process can efficiently maintain the quality of stallion extended semen for up to 4 days under cool storage.
  • This can have significant implications in the artificial insemination industry, making the storage and transportation of sperm more efficient, while ensuring high-quality samples.

Cite This Article

APA
Len J, Beehan D, Eilts B, Ebrahimie E, Lyle S. (2019). Stallion Sperm Integrity After Centrifugation to Reduce Seminal Plasma Concentration and Cool Storage for 4 days. J Equine Vet Sci, 85, 102819. https://doi.org/10.1016/j.jevs.2019.102819

Publication

ISSN: 0737-0806
NlmUniqueID: 8216840
Country: United States
Language: English
Volume: 85
Pages: 102819

Researcher Affiliations

Len, Jose
  • Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge. Electronic address: jose@lenmedvet.com.
Beehan, David
  • Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge.
Eilts, Bruce
  • Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge.
Ebrahimie, Esmaeil
  • School of Animal and Veterinary Sciences, School of Medicine, The University of Adelaide, Adelaide, Australia.
Lyle, Sara
  • Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge.

MeSH Terms

  • Animals
  • Centrifugation / veterinary
  • Horses
  • Male
  • Semen
  • Semen Analysis / veterinary
  • Sperm Motility
  • Spermatozoa