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Theriogenology2002; 57(3); 1135-1142; doi: 10.1016/s0093-691x(01)00689-6

Effect of storage time and temperature on stallion sperm DNA and fertility.

Abstract: We used the sperm chromatin structure assay (SCSA) to study the change in stallion sperm DNA susceptibility to denaturation after exposure of extended semen to three different storage temperatures (5, 20, or 37 degrees C) at 7, 20, 31, and 46 h. In addition, we compared the rates of sperm DNA denaturation in fertile and subfertile stallions. Among fertile stallions, spermatozoa stored at 20 and 37 degrees C showed a significant (P 0.05) changes in the SCSA values measured over time, indicating maintenance of chromatin quality for up to 46 h. The COMP(alpha(t)) from stallions classified as subfertile showed an increased susceptibility to denaturation or decline in chromatin quality between 20 and 31 h when stored at 5 degrees C; however, spermatozoa from fertile stallions did not change during the time intervals analyzed. These data suggest that sperm DNA from some subfertile stallions may decline at a greater rate than spermatozoa from fertile stallions when exposed to similar storage conditions.
Publication Date: 2002-06-04 PubMed ID: 12041906DOI: 10.1016/s0093-691x(01)00689-6Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article discusses a study into how different storage temperatures and time affect the DNA of stallion sperm, and how this impacts fertility. Storage conditions appeared to affect the DNA of sperm from subfertile and fertile stallions differently.

Research Methodology

  • The researchers used an approach known as the sperm chromatin structure assay (SCSA) to study changes in the DNA of stallion sperm after being stored at different temperatures.
  • The temperatures were 5, 20, or 37 degrees Celsius, with tests taking place at 7, 20, 31, and 46 hours into storage.
  • They also compared DNA changes in sperm of fertile and subfertile stallions.

Findings and Analysis

  • The results showed that for fertile stallions, storing sperm at 20 and 37 degrees Celsius significantly increased DNA denaturation rates over time. This effect was found to be more pronounced at 37 degrees Celsius.
  • For all the stallions in the study irrespective of fertility, the DNA measure of chromatin quality, observed through SCSA values, did not significantly differ when the sperm was stored at 5 degrees Celsius for up to 46 hours, showing that this temperature maintains the quality of the sperm’s DNA over time.
  • Subfertile Stallions Results

    • Subfertile stallions had a striking response. When their sperm was stored at 5 degrees Celsius, between 20 and 31 hours, their chromatin quality showed a noticeable decline or increased susceptibility to denaturation. This did not occur in the fertile stallions.
    • The researchers concluded that sperm DNA from some subfertile stallions seem to degrade faster than sperm from fertile stallions when exposed to the same storage conditions.

Cite This Article

APA
Lo CC, Thompson JA, Lowry VK, Varner DD. (2002). Effect of storage time and temperature on stallion sperm DNA and fertility. Theriogenology, 57(3), 1135-1142. https://doi.org/10.1016/s0093-691x(01)00689-6

Publication

ISSN: 0093-691X
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 57
Issue: 3
Pages: 1135-1142

Researcher Affiliations

Lo, C C
  • Department of Physiology and Pharmacology, Texas A&M University College of Veterinary Medicine, College Station 77843, USA. charles-c-love@tamu.edu
Thompson, J A
    Lowry, V K
      Varner, D D

        MeSH Terms

        • Animals
        • Chromatin / chemistry
        • DNA / analysis
        • DNA / chemistry
        • Fertility
        • Horse Diseases
        • Horses / physiology
        • Infertility / veterinary
        • Male
        • Nucleic Acid Denaturation
        • Semen Preservation / methods
        • Semen Preservation / veterinary
        • Spermatozoa / chemistry
        • Spermatozoa / physiology
        • Temperature
        • Time Factors

        Citations

        This article has been cited 6 times.
        1. Brogna R, Fan J, Sieme H, Wolkers WF, Oldenhof H. Drying and temperature induced conformational changes of nucleic acids and stallion sperm chromatin in trehalose preservation formulations. Sci Rep 2021 Jul 7;11(1):14076.
          doi: 10.1038/s41598-021-93569-ypubmed: 34234244google scholar: lookup
        2. González-Marín C, Gosálvez J, Roy R. Types, causes, detection and repair of DNA fragmentation in animal and human sperm cells. Int J Mol Sci 2012 Oct 31;13(11):14026-52.
          doi: 10.3390/ijms131114026pubmed: 23203048google scholar: lookup
        3. Minervini F, Dell'Aquila ME. Zearalenone and reproductive function in farm animals. Int J Mol Sci 2008 Dec;9(12):2570-2584.
          doi: 10.3390/ijms9122570pubmed: 19330093google scholar: lookup
        4. Brito LFC, Linardi RL, Rosales LAS, Balamurugan NS, Hernández-Avilés C, Ramírez-Agámez L. Evaluation of a Chemically Defined, Long-Term Extender for Liquid Storage of Stallion Semen. Reprod Domest Anim 2025 Sep;60(9):e70126.
          doi: 10.1111/rda.70126pubmed: 41002042google scholar: lookup
        5. Medica AJ, Gibb Z, Aitken RJ. Optimizing equine sperm quality: an alternative to single layer centrifugation for sperm isolation. Reprod Fertil 2024 Oct 1;5(4).
          doi: 10.1530/RAF-23-0081pubmed: 39437190google scholar: lookup
        6. Johannisson A, Morrell JM, Ntallaris T. A combination of biomarkers for predicting stallion sperm fertility. Vet Res Commun 2024 Aug;48(4):2157-2169.
          doi: 10.1007/s11259-024-10372-6pubmed: 38652412google scholar: lookup