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Motility, morphology and triple stain analysis of fresh, cooled and frozen-thawed stallion spermatozoa.

Abstract: The aim of the present study was to determine whether there are characteristics of fresh, cooled and frozen-thawed semen samples that can be used to predict the suitability of stallion semen for preservation by cooling or freezing. Each of three ejaculates obtained from 12 stallions was divided into aliquots to be analysed for sperm motility, morphology and membrane integrity as fresh, cooled and frozen-thawed samples. The percentage of morphologically normal spermatozoa was similar in fresh and cooled samples and both were greater than in the frozen samples. There were no strong linear relationships in the percentages of progressive motility, live spermatozoa and morphologically normal spermatozoa in fresh, cooled and frozen-thawed semen samples. Although the percentages of motile spermatozoa in fresh, cooled and frozen samples were linearly related, when sperm motility was ranked as excellent, good, fair and poor, the only correlation observed was between progressive sperm motility in fresh samples and total sperm motility in frozen samples. The results of the present study demonstrate that the high percentage of progressive motility in fresh semen samples is not indicative of similar patterns in cooled or frozen-thawed samples. Commonly used methods for assessing sperm function do not appear to be useful for predicting the ability of stallion semen to withstand preservation by either cooling or freezing.
Publication Date: 2000-01-01 PubMed ID: 20681122
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  • Journal Article

Summary

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The research study aimed to identify the key factors that could determine the suitability of stallion semen for preservation by cooling or freezing. However, the study found no significant predictors and concluded that high percentage of progressive motility in fresh semen samples is not indicative of similar patterns in cooled or frozen-thawed samples.

Study Design

  • This study involved obtaining three ejaculates from 12 stallions, dividing them into aliquots, and then analyzing the fresh, cooled, and frozen-thawed semen samples for sperm motility, morphology, and membrane integrity.
  • Through this methodology, researchers aimed to identify any strong linear relationships or characteristics that might predict the best conditions for semen preservation.

Findings

  • While the percentage of morphologically normal spermatozoa was similar in both fresh and cooled samples and greater than that in the frozen samples, no strong linear relationships were found in terms of progressive motility, live spermatozoa, and morphologically normal spermatozoa across the three states.
  • Similarly, while there was a linear relation between the percentages of motile spermatozoa in fresh, cooled and frozen samples, no correlation was observed when sperm motility was ranked as excellent, good, fair, and poor, except for a link between progressive sperm motility in fresh samples and total sperm motility in frozen samples.

Conclusion

  • This research concludes that the high percentage of progressive motility in fresh semen samples does not necessarily lead to similar patterns in cooled or frozen-thawed samples.
  • The study therefore rejects its initial hypothesis and concludes that the commonly used methods of assessing sperm function are not useful for predicting the preservation ability of stallion semen under different conditions.

Cite This Article

APA
Brinsko SP, Van Wagner GS, Graham JK, Squires EL. (2000). Motility, morphology and triple stain analysis of fresh, cooled and frozen-thawed stallion spermatozoa. J Reprod Fertil Suppl(56), 111-120.

Publication

ISSN: 0449-3087
NlmUniqueID: 0225652
Country: England
Language: English
Issue: 56
Pages: 111-120

Researcher Affiliations

Brinsko, S P
  • Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, CO 80523, USA.
Van Wagner, G S
    Graham, J K
      Squires, E L

        MeSH Terms

        • Animals
        • Cryopreservation / methods
        • Cryopreservation / veterinary
        • Freezing
        • Horses / physiology
        • Male
        • Refrigeration
        • Semen Preservation / methods
        • Semen Preservation / veterinary
        • Sperm Motility / physiology
        • Spermatozoa / cytology
        • Spermatozoa / physiology
        • Staining and Labeling / veterinary

        Citations

        This article has been cited 2 times.
        1. Medica AJ, Aitken RJ, Nicolson GL, Sheridan AR, Swegen A, De Iuliis GN, Gibb Z. Glycerophospholipids protect stallion spermatozoa from oxidative damage in vitro. Reprod Fertil 2021 Jul;2(3):199-209.
          doi: 10.1530/RAF-21-0028pubmed: 35118390google scholar: lookup
        2. Gibb Z, Aitken RJ. The Impact of Sperm Metabolism during In Vitro Storage: The Stallion as a Model. Biomed Res Int 2016;2016:9380609.
          doi: 10.1155/2016/9380609pubmed: 26881234google scholar: lookup