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Induction and characterization of acrosome reaction in equine spermatozoa.

Abstract: Equine spermatozoa were incubated in a chemically defined medium for 8 hours. The medium preserved spermatozoal viability, as assessed by total spermatozoal motility, progressive spermatozoal motility, and spermatozoal exclusion of eosin stain. Effects of time and divalent cation ionophore, A23187, on the occurrence and character of the spermatozoal acrosome reaction were determined. Two light microscopic assays, a triple-stain technique and a chlortetracycline fluorescence assay, were calibrated with transmission electron microscopy for detection of the acrosome reaction. Incubation time and A23187 addition increased the percentage of acrosome reactions in sperm populations (P less than 0.05).
Publication Date: 1987-09-01 PubMed ID: 3116891
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research paper is about the induction and analysis of the acrosome reaction in horse spermatozoa. It examines the effects of different factors such as time and ionophore on the acrosome reaction.

Introduction

  • This research focuses on equine spermatozoa and how the acrosome reaction in these sperm cells can be induced and characterized.
  • The acrosome reaction is extremely crucial for normal sperm function since it allows the sperm to penetrate the outer layers of the egg.

Methodology

  • The sperm cells were incubated in a chemically defined medium for a total of 8 hours.
  • The viability of these spermatozoa was assessed by their ability to move, both total and in a progressive direction, as well their ability to exclude the eosin stain which indicates viability.
  • The team employed two light microscopic assays – a triple-stain technique and a chlortetracycline fluorescence assay. To detect the acrosome reaction, these were calibrated with transmission electron microscopy.

Findings

  • The researchers observed the effects of time spent in the medium and the addition of the divalent cation ionophore, A23187, on the acrosome reaction in spermatozoa.
  • Both the incubation time and the addition of A23187 increased the percentage of acrosome reactions in sperm populations. The P-value (representing the probability that the observed results were down to chance) was less than 0.05, indicating that the results were statistically significant.

Conclusion

  • This study provides valuable insights into how the acrosome reaction in equine spermatozoa can be induced and characterized.
  • Such knowledge can be useful in the field of animal breeding and in enhancing reproductive success for horses.

Cite This Article

APA
Varner DD, Ward CR, Storey BT, Kenney RM. (1987). Induction and characterization of acrosome reaction in equine spermatozoa. Am J Vet Res, 48(9), 1383-1389.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 48
Issue: 9
Pages: 1383-1389

Researcher Affiliations

Varner, D D
  • Section of Reproductive Studies, University of Pennsylvania School of Veterinary Medicine, New Bolton Center, Kennett Square 19348.
Ward, C R
    Storey, B T
      Kenney, R M

        MeSH Terms

        • Acrosome / drug effects
        • Acrosome / physiology
        • Acrosome / ultrastructure
        • Animals
        • Calcimycin / pharmacology
        • Horses / physiology
        • Male
        • Sperm Capacitation
        • Sperm Motility
        • Spermatozoa / physiology

        Citations

        This article has been cited 3 times.
        1. Álvarez-Guerrero A, González-Díaz F, Medrano A, Moreno-Mendoza N. In vitro capacitation and acrosome reaction in sperm of the phyllostomid bat Artibeus jamaicensis.. In Vitro Cell Dev Biol Anim 2016 Apr;52(4):454-65.
          doi: 10.1007/s11626-015-9991-ypubmed: 26744028google scholar: lookup
        2. McPartlin LA, Visconti PE, Bedford-Guaus SJ. Guanine-nucleotide exchange factors (RAPGEF3/RAPGEF4) induce sperm membrane depolarization and acrosomal exocytosis in capacitated stallion sperm.. Biol Reprod 2011 Jul;85(1):179-88.
          doi: 10.1095/biolreprod.110.085555pubmed: 21471298google scholar: lookup
        3. Grøndahl C, Grøndahl ML, Hyttel P, Greve T. Acrosomal status in fresh and frozen/thawed stallion spermatozoa evaluated by scanning electron microscopy.. Anat Embryol (Berl) 1994 Aug;190(2):195-200.
          doi: 10.1007/BF00193415pubmed: 7818091google scholar: lookup