Analyze Diet
Environmental monitoring and assessment2025; 197(9); 1058; doi: 10.1007/s10661-025-14509-1

Effects of vitamin E and selenium supplementation on oxidative stress parameters and marker of genomic instability in show jumping equines exposed to different sources of atmospheric pollution.

Abstract: The inhalation of pollutants from fossil fuel combustion increases oxidative stress and may cause genotoxic damage, a risk heightened during physical exercise due to increased respiratory rates. This concern extends to equines engaged in intense activities like show jumping. Antioxidant supplementation with vitamin E and selenium may mitigate oxidative stress induced by exercise in polluted environments. This study evaluated the effects of oral supplementation on show jumping horses subjected to physical exertion in urban (n = 10) and peri-urban (n = 10) areas with varying pollution levels. Oxidative stress markers (protein quantification, superoxide dismutase, catalase, and thiobarbituric acid reactive substances), marker of genomic instability (binucleation), and clinical parameters were assessed in relation to environmental nitrogen dioxide (NO) and ozone (O) levels. Results showed that supplementation influenced thiobarbituric acid reactive substances (TBARS), with lower malondialdehyde (MDA) concentration in supplemented groups, especially in urban horses (p = 0.027). DNA damage was reduced in supplemented horses from urban areas with high ozone (O) levels (p = 0.002), but no protective effect was observed in peri-urban horses. These findings suggest that vitamin E and selenium supplementation have antioxidant and DNA-protective impact in urban environments, though their efficacy appears variable in peri-urban areas. Further research incorporating additional pollution markers is necessary to clarify these effects.
Publication Date: 2025-08-29 PubMed ID: 40879818DOI: 10.1007/s10661-025-14509-1Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

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.

Overview

  • This study investigated how vitamin E and selenium supplements affect oxidative stress and DNA damage in show jumping horses exposed to different air pollution levels.
  • The research found that supplementation reduced markers of oxidative damage and genomic instability in horses living in urban high-pollution areas but was less effective in peri-urban environments.

Background and Purpose

  • Equines performing intensive exercise, such as show jumping, have an increased respiratory rate, leading to greater inhalation of air pollutants from fossil fuel combustion.
  • Pollutants like nitrogen dioxide (NO₂) and ozone (O₃) contribute to oxidative stress—an imbalance favoring harmful reactive oxygen species—and may cause genotoxic damage to DNA.
  • Vitamin E and selenium are known antioxidants that potentially mitigate oxidative stress, possibly protecting cellular components like lipids and DNA from damage.
  • The study aimed to examine whether oral supplementation with vitamin E and selenium lessens oxidative stress and DNA damage in horses exposed to different pollution levels during exercise.

Study Design and Methods

  • Participants: Twenty show jumping horses were divided into two groups based on their environment:
    • Urban area group (n=10): exposed to higher pollution levels.
    • Peri-urban area group (n=10): exposed to relatively lower pollution levels.
  • Intervention: Oral supplementation with vitamin E and selenium.
  • Assessments conducted included:
    • Oxidative stress markers:
      • Protein quantification
      • Superoxide dismutase (SOD) activity
      • Catalase (CAT) activity
      • Thiobarbituric acid reactive substances (TBARS), primarily measuring malondialdehyde (MDA), a lipid peroxidation product
    • Genomic instability marker:
      • Binucleation rate, indicating DNA damage
    • Clinical parameters for overall health status.
  • Environmental measurements of NO₂ and ozone levels were taken to correlate pollution exposure with biological effects.

Key Results

  • Supplementation Effects on Oxidative Stress:
    • Vitamin E and selenium supplementation lowered TBARS levels, indicating reduced lipid peroxidation.
    • The reduction in MDA concentration was statistically significant in horses from urban areas (p=0.027), suggesting effective mitigation of oxidative stress under high pollution.
  • Genomic Instability Findings:
    • Horses supplemented in urban environments with high ozone levels exhibited significant decreases in binucleation rates, indicating lower DNA damage (p=0.002).
    • No protective effect on DNA damage was observed in peri-urban horses despite supplementation.
  • Overall, the supplementation demonstrated a protective antioxidant and DNA-stabilizing effect primarily in horses exposed to more polluted urban environments.

Interpretation and Implications

  • The findings imply that antioxidant supplementation with vitamin E and selenium can counteract some harmful effects of pollution-induced oxidative stress and genomic instability in exercising horses living in urban areas.
  • The lack of observed benefit in peri-urban horses may be due to:
    • Lower pollution levels making oxidative damage less pronounced and harder to detect changes.
    • Different pollutant profiles or other environmental factors influencing supplementation efficacy.
  • This suggests that supplementation strategies might need tailoring based on pollution exposure and environmental context.
  • Further research should:
    • Include a broader range of pollution markers to better characterize environmental exposures.
    • Explore long-term effects of antioxidant supplementation.
    • Investigate mechanistic pathways of protection and dose optimization for equines exposed to diverse conditions.

Conclusion

  • Vitamin E and selenium supplementation shows promise as a protective intervention against oxidative stress and DNA damage in show jumping horses exposed to urban atmospheric pollution during exercise.
  • The variable effectiveness depending on environmental pollution levels highlights the complexity of antioxidant interventions and the need for customized approaches.

Cite This Article

APA
Dos Santos Gomes V, Dos Santos Marques JV, da Silva GN, Marmett B, Dallegrave E. (2025). Effects of vitamin E and selenium supplementation on oxidative stress parameters and marker of genomic instability in show jumping equines exposed to different sources of atmospheric pollution. Environ Monit Assess, 197(9), 1058. https://doi.org/10.1007/s10661-025-14509-1

Publication

ISSN: 1573-2959
NlmUniqueID: 8508350
Country: Netherlands
Language: English
Volume: 197
Issue: 9
Pages: 1058

Researcher Affiliations

Dos Santos Gomes, Victória
  • Graduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande Do Sul, Brazil.
  • Toxicology Research Laboratory, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande Do Sul, Brazil.
Dos Santos Marques, José Vítor
  • Toxicology Research Laboratory, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande Do Sul, Brazil.
da Silva, Gedaias Noronha
  • Graduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande Do Sul, Brazil.
  • Toxicology Research Laboratory, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande Do Sul, Brazil.
Marmett, Bruna
  • Project Office, Social Responsibility, PROADI-SUS, Hospital Moinhos de Vento, Porto Alegre, Rio Grande Do Sul, Brazil.
  • Graduate Program in Pediatrics - Federal, University of Health Sciences of Porto Alegre, Porto Alegre, Rio Grande Do Sul, Brazil.
Dallegrave, Eliane
  • Graduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande Do Sul, Brazil. elianedal@ufcspa.edu.br.
  • Toxicology Research Laboratory, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, Rio Grande Do Sul, Brazil. elianedal@ufcspa.edu.br.
  • Pharmacosciences Department, Federal University of Health Sciences of Porto Alegre, Rua Sarmento Leite, 245, Porto Alegre, CEP, 90050-170, Brazil. elianedal@ufcspa.edu.br.

MeSH Terms

  • Animals
  • Vitamin E / pharmacology
  • Oxidative Stress / drug effects
  • Horses
  • Selenium
  • Air Pollutants / toxicity
  • Air Pollutants / analysis
  • Genomic Instability / drug effects
  • Air Pollution / statistics & numerical data
  • Antioxidants
  • Dietary Supplements
  • Ozone / toxicity
  • Biomarkers / metabolism
  • DNA Damage
  • Nitrogen Dioxide / toxicity

Conflict of Interest Statement

Declarations. Competing interests: The authors declare no competing interests. Clinical trial number: Not applicable.

References

This article includes 39 references
  1. ABCCH. (2012). Associação Brasileira de Criadores do Cavalo de Hipismo. https://www.abcch.com.br
  2. Aebi H. Catalase in vitro. Methods in Enzymology 105, 121–126.
  3. Alves LMD. Bioquímica sangüínea de eqüinos: influências da raça, idade e sexo. .
  4. Amorim MCDCT. O clima urbano de Presidente Prudente/SP. .
  5. Bailey DM, Williams C, Betts JA, Thompson D, Hurst TL. Oxidative stress, inflammation and recovery of muscle function after damaging exercise: Effect of 6-week mixed antioxidant supplementation. European Journal of Applied Physiology 111(6), 925–936.
    doi: 10.1007/s00421-010-1718-xgoogle scholar: lookup
  6. Baird C, Cann M. Química ambiental. .
  7. Bolognesi C, Knasmueller S, Nersesyan A, Thomas P, Fenech M. The HUMNxl scoring criteria for different cell types and nuclear anomalies in the buccal micronucleus cytome assay - An update and expanded photogallery. Mutation Research 753(2), 100–113.
  8. Brazil National Council for the Environment (CONAMA). Resolution No. 491, of November 19, 2018. Establishes national air quality standards. .
  9. Brusick DJ. Genetic toxicology. Toxicology pp. 127–149.
  10. Carrard VC, Ferreira LA, Lauxen IDS, Costa CH, Rados PV. Micronucleus assay: A biomarker of genotoxic damage in exfoliated oral mucosa cells. Revista da Faculdade de Odontologia de Porto Alegre 48(13), 77–81.
  11. Castier Y, Brandes RP, Leseche G, Tedgui A, Lehoux S. p47phox-dependent NADPH oxidase regulates flow-induced vascular remodeling. Circulation Research 97(6), 533–540.
  12. Clayton H. Conditioning sport horses. 1st ed..
  13. De Leon JAD, Borges CR. Evaluation of oxidative stress in biological samples using the thiobarbituric acid reactive substances assay. Journal of visualized experiments: JoVE 159, 10–3791.
    doi: 10.3791/61122google scholar: lookup
  14. De Moffarts B, Portier K, Kirschvink N, Coudert J, Fellmann N, van Erck E, Letellier C, Motta C, Pincemail J, Art T, Lekeux P. Effects of exercise and oral antioxidant supplementation enriched in (n−3) fatty acids on blood oxidant markers and erythrocyte membrane fluidity in horses. The Veterinary Journal 174(1), 113–121.
  15. Duncan JR, Prasse KW, Mahaffey EA. Veterinary laboratory medicine: Clinical pathology. 3rd ed..
  16. Fenech M, Chang WP, Kirsch-Volders M, Holland N, Bonassi S, Zeiger E. HUMN project: Detailed description of the scoring criteria for the cytokinesis-block micronucleus assay using isolated human lymphocyte cultures. Mutation Research/genetic Toxicology and Environmental Mutagenesis 534(1–2), 65–75.
  17. Filho JBG. POLUIÇÃO DO AR. .
  18. WC Jr G. Gas-phase combustion chemistry. .
    doi: 10.1007/978-1-4612-1310-9google scholar: lookup
  19. Gomez-Cabrera M-C, Domenech E, Romagnoli M, Arduini A, Borras C, Pallardo FV, Sastre J, Viña J. Oral administration of vitamin C decreases muscle mitochondrial biogenesis and hampers training-induced adaptations in endurance performance. The American Journal of Clinical Nutrition 87(1), 142–149.
    doi: 10.1093/ajcn/87.1.142google scholar: lookup
  20. Gonzalez FHD, Silva SC. Introdução à bioquímica clínica veterinária (ePub). .
  21. Ji LL, Gomez-Cabrera M, Viña J. Exercise and hormesis. Annals of the New York Academy of Sciences 1067(1), 425–435.
    doi: 10.1196/annals.1354.061google scholar: lookup
  22. Liu C, Chen R, Sera F, Vicedo-Cabrera AM, Guo Y, Tong S, Kan H. Ambient particulate air pollution and daily mortality in 652 cities. New England Journal of Medicine 381(8), 705-715.
    doi: 10.1056/nejmoa1817364google scholar: lookup
  23. Lodge J. Methods of air sampling and analysis. .
  24. Lombardo MA. Qualidade ambiental e planejamento urbano: considerações de método. .
  25. Mak MK, Wong-Yu IS. Exercise for Parkinson's disease. International review of neurobiology 147, 1-44.
  26. Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. European Journal of Biochemistry 47(3), 469–474.
  27. Meng Q, Su C-H. The impact of physical exercise on oxidative and nitrosative stress: Balancing the benefits and risks. Antioxidants 13(5), 573.
    doi: 10.3390/antiox13050573google scholar: lookup
  28. Pandya RJ, Solomon G, Kinner A, Balmes JR. Diesel exhaust and asthma: Hypotheses and molecular mechanisms of action. Environmental Health Perspectives 110(suppl 1), 103–112.
    doi: 10.1289/ehp.02110s1103google scholar: lookup
  29. Premoli-De-Percoco G, Ramírez JL, Galindo I. Correlation between HPV types associated with oral squamous cell carcinoma and cervicovaginal cytology. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology 86(1), 77–81.
  30. Radak Z, Chung HY, Koltai E, Taylor AW, Goto S. Exercise, oxidative stress and hormesis. Ageing Research Reviews 7(1), 34–42.
    doi: 10.1016/j.arr.2007.04.004google scholar: lookup
  31. Ribeiro WC. Apresentação: o patrimônio ambiental brasileiro. .
  32. Rose RJ, Hodgson DR. Manual of equine practice. .
  33. Schleicher E, Wieland OH. Evaluation of the Bradford method for protein determination in body fluids. Journal of Clinical Chemistry and Clinical Biochemistry 16(9), 533–534.
  34. Schmidt HHHW, Walter U. NO at work. Cell 78(6), 919–925.
  35. Schneider CD, de Oliveira AR. Radicais livres de oxigênio e exercício: Mecanismos de formação e adaptação ao treinamento físico. Revista Brasileira De Medicina Do Esporte 10(4), 308–313.
  36. Smaka-Kincl V, Stegnar P, Lovka M, Toman MJ. The evaluation of waste, surface and ground water quality using the Allium test procedure. Mutation Research/genetic Toxicology 368(3–4), 171–179.
  37. Torres-Bugarín O, Zavala-Cerna MG, Nava A, Flores-García A, Ramos-Ibarra ML. Potential uses, limitations, and basic procedures of micronuclei and nuclear abnormalities in buccal cells. Disease Markers 2014(1), 956835.
  38. Valko M, Leibfritz D, Moncol J, Cronin MTD, Mazur M, Telser J. Free radicals and antioxidants in normal physiological functions and human disease. The International Journal of Biochemistry & Cell Biology 39(1), 44–84.
  39. . Air quality guidelines for particulate matter, ozone, nitrogen dioxide and sulfur dioxide: global update 2005. .

Citations

This article has been cited 0 times.