Assessment of extent of apoptosis and DNA defragmentation in chilled semen of stallions during the breeding season.
Abstract: The objective of the study was to assess apoptosis and DNA defragmentation in equine semen diluted and chilled to +4°C. Semen was collected from nine fertile stallions, including four Arabian thoroughbreds and five coldbloods. Examinations were carried out immediately after semen collection (0) and at five storage times (24, 48, 72, 96 and 120 h). The basic semen evaluation was performed in terms of volume, sperm concentration, viable sperm percentage, progressive motility and morphology. Using flow cytometry, DNA defragmentation and cell membrane integrity of spermatozoa were determined. The results of basic tests did not demonstrate significant differences amongst stallions, except for progressive sperm motility, which was significantly higher (p < 0.05) in the semen of Arabian stallions. In the semen of the same stallions, a significant decrease in the percentage of alive spermatozoa was observed at 72, 96 and 120 h of storage, whereas a significant increase in the number of spermatozoa with DNA defragmentation was found after 24 h storage. In the semen of coldblood stallions, significantly reduced live spermatozoa percentage was observed at 96 and 120 h, while increased DNA defragmentation was observed at 48 h. These findings demonstrated that the semen of Arabian stallions chilled to +4°C retained original characteristics until 24 h of storage, whereas in coldbloods, these were preserved up to 48 h of storage.
© 2013 Blackwell Verlag GmbH.
Publication Date: 2013-03-26 PubMed ID: 23531092DOI: 10.1111/rda.12170Google Scholar: Lookup
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Summary
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The research article presents a study focusing on the impacts of chilling on stallion semen, specifically examining apoptosis (cell death) and DNA defragmentation. The findings indicated that semen characteristics were retained until 24 hours of chilling for Arabian stallions and until 48 hours for coldblood stallions.
Objective and Methodology of the Study
- The study aimed to investigate the level of apoptosis and DNA defragmentation in equine semen that was diluted and chilled to +4°C.
- Semen was collected from nine fertile stallions, which included four Arabian thoroughbreds and five coldbloods.
- The semen samples were examined immediately after collection and at intervals of 24, 48, 72, 96, and 120 hours.
- Researchers evaluated semen for volume, sperm concentration, percentage of viable sperm, progressive motility, and morphology.
- They used flow cytometry, a technique that allows for the detailed examination of cells, to determine DNA defragmentation and cell membrane integrity of spermatozoa.
Key Findings of the Research
- The initial tests did not show significant differences amongst the stallions, except for progressive sperm motility. This was notably higher in Arabian stallions.
- In the semen of Arabian stallions, there was a significant decrease in the percentage of live spermatozoa at 72, 96, and 120 hours of chilling. There was also a significant increase in the number of spermatozoa with DNA fragmentation after 24 hours of storage.
- In contrast, in the coldblood stallions’ semen, the percentage of live spermatozoa decreased significantly at 96 and 120 hours. The DNA fragmentation increased significantly at 48 hours.
- From these results, it can be inferred that Arabian stallions’ semen retained original characteristics for up to 24 hours when chilled to +4°C, whereas coldblood stallions’ sperm retained the qualities for up to 48 hours.
Implications of the Study
- The findings of the study are essential for horse breeding practices. They suggest that the chilling time of semen should be considered for successful fertilization, depending on the breed of the stallion.
- The research contributes to understanding cell death (apoptosis) and DNA fragmentation in semen, which are important factors in sperm viability and breeding success.
- The findings could help develop optimal semen storage techniques to improve breeding outcomes.
Cite This Article
APA
Krakowski L, Obara J, Wąchocka A, Piech T, Bartoszek P, Kostro K, Tatara MR.
(2013).
Assessment of extent of apoptosis and DNA defragmentation in chilled semen of stallions during the breeding season.
Reprod Domest Anim, 48(5), 826-832.
https://doi.org/10.1111/rda.12170 Publication
Researcher Affiliations
- Department of Andrology and Biotechnology of Reproduction, Chair of Animal Reproduction, Faculty of Veterinary Medicine, University of Life Sciences in Lublin, Lublin, Poland.
MeSH Terms
- Animals
- Apoptosis / physiology
- Cold Temperature
- DNA Fragmentation
- Horses / physiology
- Male
- Semen / physiology
- Semen Analysis / veterinary
- Semen Preservation / veterinary
Citations
This article has been cited 3 times.- Ramirez-Perez H, Guerrero-Netro HM, Torres-Rodríguez P, Díaz-Durán M, Boeta-Acosta AM, Diaw M. A combination of taurine and caffeine maintains sperm quality in equine semen during chilled storage. J Adv Vet Anim Res 2021 Dec;8(4):635-641.
- Perrett J, Harris IT, Maddock C, Farnworth M, Pyatt AZ, Sumner RN. Systematic Analysis of Breed, Methodological, and Geographical Impact on Equine Sperm Progressive Motility. Animals (Basel) 2021 Oct 29;11(11).
- Atroshchenko MM, Arkhangelskaya E, Isaev DA, Stavitsky SB, Zaitsev AM, Kalaschnikov VV, Leonov S, Osipov AN. Reproductive Characteristics of Thawed Stallion Sperm. Animals (Basel) 2019 Dec 9;9(12).
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