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Theriogenology2002; 57(5); 1493-1501; doi: 10.1016/s0093-691x(02)00659-3

Capacitation and acrosomal exocytosis are enhanced by incubation of stallion spermatozoa in a commercial semen extender.

Abstract: Preserved stallion semen often has decreased spermatozoal motility and fertility that can vary significantly between individual stallions. It is not known whether the medium used for extending equine sperm contributes to these decreases by inducing premature capacitation during storage. If spermatozoa undergo capacitation or acrosome reaction prior to insemination, this could result in a diminished capacity to penetrate the cumulus mass and fertilize the egg. We hypothesized that skim milk-based semen extenders, similar to those used in cooled storage, stabilize sperm membranes and prolong sperm motility and longevity. However, this could decrease the efficiency of sperm to undergo subsequent capacitation in vivo. This study was designed to evaluate the effects from two media on sperm function. Spermatozoal motility was analyzed, intracellular calcium was measured, and the ability of sperm to undergo acrosome reaction was compared after incubation in a skim milk extender (SME) and Tyrode's medium containing albumin, lactate, and pyruvate (TALP) at 37 degrees C. Results suggest that the SME facilitated capacitation as detected by an increase in both intracellular calcium and acrosome reactions, and a decrease in motility, as compared to TALP. Our data support a shortened functional lifespan for equine sperm in skim milk extender, which indicates that further refinements in cooled semen preservation are required to improve fertility of transported equine semen.
Publication Date: 2002-06-11 PubMed ID: 12054207DOI: 10.1016/s0093-691x(02)00659-3Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.

Summary

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The research investigates the impact of different mediums on the health and functionality of stallion sperm cells. The findings suggest that a medium called skim milk extender enhances natural sperm processes, but may shorten their lifespan.

Introduction

  • The study seeks to explore the reasons for the decreased motility and fertility often observed in preserved stallion semen.
  • One potential cause is suspected to be the medium in which the sperm is extended, with the hypothesis being that this could induce premature capacitation during storage.
  • The research proposes that premature capacitation and acrosome reaction can limit fertility by reducing the sperm’s capacity to penetrate the egg.

Hypothesis and Experiment Design

  • The researchers speculate that skim milk-based semen extenders, used during cooled storage may stabilize sperm membranes, thus slowing down their motility and extending their longevity. But, their efficiency in vivo may consequently be hampered.
  • To investigate these effects, the research involved evaluating sperm function after incubation in skim milk extender and Tyrode’s medium (containing albumin, lactate, and pyruvate) at 37 degrees Celsius.

Methods and Findings

  • Sperm motility was analyzed, intracellular calcium levels were measured, and the ability of sperm to undergo acrosome reaction was compared between the two mediums.
  • The results suggested that skim milk extender facilitated capacitation, demonstrated by an increase in both intracellular calcium and acrosome reactions, and a decrease in motility, as compared to Tyrode’s medium.

Conclusion

  • The findings supported the theory of a shortened functional lifespan for horse sperm in the skim milk extender medium.
  • This might entail a need for refinement in cooled semen preservation techniques for improving the fertility of transported equine semen.

Cite This Article

APA
Pommer AC, Linfor JJ, Meyers SA. (2002). Capacitation and acrosomal exocytosis are enhanced by incubation of stallion spermatozoa in a commercial semen extender. Theriogenology, 57(5), 1493-1501. https://doi.org/10.1016/s0093-691x(02)00659-3

Publication

ISSN: 0093-691X
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 57
Issue: 5
Pages: 1493-1501

Researcher Affiliations

Pommer, Angela C
  • Department of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California, Davis 95616, USA.
Linfor, Jennifer J
    Meyers, Stuart A

      MeSH Terms

      • Acrosome / metabolism
      • Albumins
      • Animals
      • Calcium / analysis
      • Cell Survival
      • Cold Temperature
      • Horses / physiology
      • Isotonic Solutions
      • Lactic Acid
      • Male
      • Milk
      • Pyruvic Acid
      • Semen Preservation / methods
      • Semen Preservation / veterinary
      • Solutions
      • Sperm Capacitation
      • Sperm Motility
      • Spermatozoa / physiology

      Citations

      This article has been cited 3 times.
      1. Orsolini MF, Meyers SA, Dini P. An Update on Semen Physiology, Technologies, and Selection Techniques for the Advancement of In Vitro Equine Embryo Production: Section II. Animals (Basel) 2021 Nov 20;11(11).
        doi: 10.3390/ani11113319pubmed: 34828049google scholar: lookup
      2. Varisli O, Agca C, Agca Y. Short-term storage of rat sperm in the presence of various extenders. J Am Assoc Lab Anim Sci 2013 Nov;52(6):732-7.
        pubmed: 24351761
      3. Klusackova B, Pilsova A, Zelenkova N, Pilsova Z, Krejcirova R, Chmelikova E, Komrskova K, Simonik O, Postlerova P. Time to revise: impact of methodology on boar sperm capacitation in vitro via phosphotyrosine patterns. BMC Vet Res 2025 Jul 7;21(1):448.
        doi: 10.1186/s12917-025-04900-ypubmed: 40624494google scholar: lookup