Effect of urine contamination on stallion semen freezing ability.
Abstract: Urospermia is a common ejaculatory dysfunction of stallions. Current practice suggests that urine contaminated semen should not be used for cryopreservation. The aim of this study was to determine effects of urine contamination on semen freezing. Sixty-five ejaculates from eight stallions were divided into no urine (CONT), low (20% urine, LOW), and high (50% urine, HIGH) samples. Semen was extended with a commercial cooling extender, cushion-centrifuged, resuspended to 200 million/mL in a commercial egg-yolk based extender, and cryopreserved in liquid nitrogen. A subset of ejaculates (n = 20) were split in two after cushion-centrifugation, and one half of the ejaculate was submitted to a single-layer gradient centrifugation before cryopreservation. Sperm motility parameters were assessed pre- and post-freezing with an automated sperm analyzer. Semen pH, creatinine, and urea concentrations were assessed in raw samples, after urine contamination and after centrifugation and extension. Statistical analyses were performed with ANOVA and Tukey's posthoc. There were significant reductions in total and progressive sperm motilities (i.e., %TM and %PM, respectively) with increasing urine contamination pre-freezing (%TM 67 ± 1.7, %PM 50 ± 2.2, CONT), (%TM 60.3 ± 1.7, % PM 42.5 ± 2.1, LOW), and (%TM 41.3 ± 2, %PM 21.3 ± 1.5, HIGH). Post-thaw motilities for CONT (%TM 54 ± 2.3, %PM 40.8 ± 3.3) and LOW (%TM 51.7 ± 1.8, %PM 36.2 ± 2.1) were not different, but were higher than the HIGH (%TM 31.5 ± 1.2, %PM 17.1 ± 1.0) (p < 0.05). Post-thaw sperm viability was significantly lower in the HIGH (54.7 ± 2.4) than in the CONT (63.8 ± 2.3) or LOW (64.6 ± 3.4) groups. Semen creatinine and urine levels were significantly higher with increasing urine contamination and were significantly decreased after centrifugation and resuspension in freezing extender. Pre-treatment semen pH was significantly lower than semen contaminated with low or high amounts of urine, and pH decreased significantly after centrifugation and resuspension. Gradient centrifugation did not improve %TM in the control group, but it did improve pre-freeze %TM and %PM in the low and high groups and improved significantly post freezing %TM and %PM in the high urine contaminated group. Semen contaminated with a small amount of urine may be suitable for freezing, whereas highly contaminated semen might not be usable. Although urine was mostly removed in this fashion, the initial exposure to high quantities was sufficient to decrease sperm motility pre- and post-freezing, whereas low urine contamination was not as detrimental.
Copyright © 2018 Elsevier Inc. All rights reserved.
Publication Date: 2018-05-17 PubMed ID: 29800826DOI: 10.1016/j.theriogenology.2018.05.010Google Scholar: Lookup
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- Journal Article
Summary
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The research article investigates the impact of urine contamination on the freezing ability of stallion semen. The findings suggest that while semen contaminated with a small amount of urine may still be suitable for freezing, high levels of urine contamination can significantly impact its freezing ability by reducing sperm motility.
Research Methodology
- The study was conducted on 65 ejaculates from eight stallions which were divided into three samples – no urine (CONT), low urine (20% urine, LOW), and high urine (50% urine, HIGH).
- The semen was extended with a commercial cooling extender, cushion-centrifuged, resuspended to 200 million/mL in a commercial egg-yolk-based extender, and eventually cryopreserved in liquid nitrogen.
- Twenty ejaculates were split in two after cushion-centrifugation, and one half was submitted to a single-layer gradient centrifugation before being cryopreserved.
- The sperm motility parameters were assessed before and after freezing using an automated sperm analyzer.
Findings
- The results showed significant reductions in total and progressive sperm motilities with increasing urine contamination before freezing.
- Post-thaw motilities for CONT and LOW were not different, but were higher than the HIGH.
- Post-thaw sperm viability was significantly lower in the HIGH than in the CONT or LOW groups.
- Semen creatinine and urine levels were significantly higher with increasing urine contamination and decreased significantly after centrifugation and resuspension in the freezing extender.
- The pH of pre-treatment semen was significantly lower than semen contaminated with low or high amounts of urine, and this pH decreased significantly after centrifugation and resuspension.
Impact of Gradient Centrifugation
- Gradient centrifugation didn’t improve %TM in the control group, but it improved pre-freeze %TM and %PM in the low and high groups.
- It significantly improved post freezing %TM and %PM in the high urine contaminated group.
Conclusion
- The initial exposure to high quantities of urine was sufficient to decrease sperm motility both before and after freezing, suggesting that highly contaminated semen might not be usable.
- However, low urine contamination was not as detrimental, suggesting that semen contaminated with a small amount of urine may still be suitable for freezing.
Cite This Article
APA
Ellerbrock RE, Honorato J, Curcio BR, Stewart JL, Souza JAT, Love CC, Lima FS, Canisso IF.
(2018).
Effect of urine contamination on stallion semen freezing ability.
Theriogenology, 117, 1-6.
https://doi.org/10.1016/j.theriogenology.2018.05.010 Publication
Researcher Affiliations
- Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana Champaign, Urbana, IL, USA.
- Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana Champaign, Urbana, IL, USA; Departamento de Clinica e Cirurgia Veterinaria, Universidade Federal do Piaui, Teresina, Piaui, Brazil.
- Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana Champaign, Urbana, IL, USA; Departamento de Clinica Veterinaria, Faculdade de Veterinaria, Universidade Federal de Pelotas, Rio Grande do Sul, Brazil.
- Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana Champaign, Urbana, IL, USA.
- Departamento de Clinica e Cirurgia Veterinaria, Universidade Federal do Piaui, Teresina, Piaui, Brazil.
- Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Texas A & M University, College Station, TX 77843, USA.
- Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana Champaign, Urbana, IL, USA.
- Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois Urbana Champaign, Urbana, IL, USA. Electronic address: canisso@illinois.edu.
MeSH Terms
- Animals
- Cryopreservation / methods
- Cryopreservation / veterinary
- Horses
- Male
- Semen / chemistry
- Semen Analysis / veterinary
- Semen Preservation / methods
- Semen Preservation / veterinary
- Sperm Motility
- Urine
Citations
This article has been cited 4 times.- Podico G, Spencer KM, Magalhaes HB, Canisso IF. Semen Quality of the First and Second Ejaculates Collected from Breeding Inactive Stallions after Cooling and Freezing. Vet Sci 2023 Feb 21;10(3).
- Gimeno BF, Bariani MV, Laiz-Quiroga L, Martínez-León E, Von-Meyeren M, Rey O, Mutto AÁ, Osycka-Salut CE. Effects of In Vitro Interactions of Oviduct Epithelial Cells with Frozen-Thawed Stallion Spermatozoa on Their Motility, Viability and Capacitation Status. Animals (Basel) 2021 Jan 3;11(1).
- Toledano-Díaz A, Castaño C, Velázquez R, Bóveda P, López-Sebastián A, Martínez-Nevado E, Villaverde-Morcillo S, Esteso MC, Santiago-Moreno J. Cryopreservation of ferret (Mustela putorius furo) sperm collected by rectal massage and electroejaculation: Comparison of a decelerating and an accelerating freezing rate protocol. Vet Med Sci 2021 Jan;7(1):256-263.
- Engel KM, Baumann S, Rolle-Kampczyk U, Schiller J, von Bergen M, Grunewald S. Metabolomic profiling reveals correlations between spermiogram parameters and the metabolites present in human spermatozoa and seminal plasma. PLoS One 2019;14(2):e0211679.
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