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Equine veterinary journal2005; 37(3); 243-249; doi: 10.2746/0425164054530605

Antioxidant and inflammatory responses of healthy horses and horses affected by recurrent airway obstruction to inhaled ozone.

Abstract: Inhaled ozone can induce oxidative injury and airway inflammation. Horses affected by recurrent airway obstruction (RAO) have a decreased pulmonary antioxidant capacity, which may render them more susceptible to oxidative challenge. It is currently unknown whether RAO-affected horses are more susceptible to oxidative stress than those unaffected by RAO. Objective: To determine whether ozone exposure induces greater oxidative stress and airway inflammation in RAO-affected horses in remission than in healthy horses. Methods: Seven healthy control horses and 7 RAO-affected horses were exposed to 0.8 ppm ozone for 2 h at rest. Results: At baseline, bronchoalveolar lavage fluid (BALF) ascorbic acid concentrations were lower in RAO-affected horses than healthy controls. Ozone appeared to preferentially oxidise glutathione rather than ascorbic acid 6 h after exposure. Individual healthy and RAO-affected horses demonstrated oxidation of BALF glutathione after ozone exposure. Overall, RAO-affected horses did not demonstrate increased oxidative stress following ozone exposure, compared with healthy horses. Ozone did not induce significant airway inflammation in either group. Conclusions: RAO-affected horses in remission are not more sensitive to ozone despite a decreased pulmonary antioxidant capacity. Sensitivity to ozone appears to be independent of initial pulmonary antioxidant status. Conclusions: Horses with high susceptibility to oxidative stress may benefit from antioxidant supplementation.
Publication Date: 2005-05-17 PubMed ID: 15892234DOI: 10.2746/0425164054530605Google Scholar: Lookup
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  • Journal Article

Summary

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This study investigates the effects of inhaled ozone on healthy horses and horses with recurrent airway obstruction (RAO), focusing on oxidative stress and airway inflammation. Contrary to expectation, the results showed that RAO-affected horses in remission did not react more sensitively to ozone despite having reduced pulmonary antioxidant capacity.

Research Objective

  • The purpose of the research was to understand whether horses with RAO- a recurring respiratory condition similar to asthma, which reduces the horse’s lung antioxidant capacity – respond differently to inhaled ozone than healthy horses. Specifically, the researchers were interested in knowing if the RAO-affected horses exhibited heightened oxidative stress and airway inflammation after inhaling ozone.

Research Methods

  • The study involved seven healthy horses and seven RAO-affected horses for comparison.
  • To investigate the effects, all fourteen horses were exposed to 0.8 ppm of ozone for two hours while at rest.
  • To measure oxidative stress, the team analyzed the bronchoalveolar lavage fluid (BALF) in each horse. BALF was used to measure the concentration of ascorbic acid (vitamin C) and glutathione, molecules that serve as antioxidants in the horse’s body.

Research Findings

  • The BALF results showed that at baseline, RAO-affected horses had lower levels of ascorbic acid compared to healthy horses.
  • Ozone was observed to primarily oxidize glutathione over ascorbic acid in the six hours following exposure.
  • Both the healthy and RAO-affected horses showed signs of glutathione oxidation in the BALF after ozone exposure, indicating oxidative stress.
  • However, RAO-affected horses did not experience more oxidative stress compared to the healthy horses post-ozone exposure.
  • No significant airway inflammation was observed in either group post-ozone exposure.

Conclusions

  • The findings suggest that despite having reduced pulmonary antioxidant capacity, horses affected by RAO in remission do not respond more sensitively to ozone than healthy horses.
  • The study suggests that the initial pulmonary antioxidant status doesn’t determine the vulnerability to ozone.
  • The authors recommend considering antioxidant supplementation for horses that exhibit a high susceptibility to oxidative stress. This conclusion is presumably made based on the observation of glutathione oxidation post-ozone exposure in both study groups.

Cite This Article

APA
Deaton CM, Marlin DJ, Smith NC, Roberts CA, Harris PA, Schroter RC, Kelly FJ. (2005). Antioxidant and inflammatory responses of healthy horses and horses affected by recurrent airway obstruction to inhaled ozone. Equine Vet J, 37(3), 243-249. https://doi.org/10.2746/0425164054530605

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 37
Issue: 3
Pages: 243-249

Researcher Affiliations

Deaton, C M
  • Centre for Equine Studies, Animal Health Trust, Lanwades Park, Kentford, Newmarket, Suffolk, UK.
Marlin, D J
    Smith, N C
      Roberts, C A
        Harris, P A
          Schroter, R C
            Kelly, F J

              MeSH Terms

              • Animals
              • Antioxidants / analysis
              • Ascorbic Acid / analysis
              • Bronchoalveolar Lavage Fluid / chemistry
              • Bronchoalveolar Lavage Fluid / cytology
              • Case-Control Studies
              • Female
              • Glutathione / metabolism
              • Horse Diseases / chemically induced
              • Horse Diseases / metabolism
              • Horses / metabolism
              • Lung Diseases, Obstructive / metabolism
              • Lung Diseases, Obstructive / physiopathology
              • Lung Diseases, Obstructive / veterinary
              • Male
              • Oxidants, Photochemical / adverse effects
              • Oxidation-Reduction
              • Oxidative Stress / drug effects
              • Ozone / adverse effects
              • Recurrence

              Citations

              This article has been cited 8 times.
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              6. Wang Q, Ju X, Chen Y, Dong X, Luo S, Liu H, Zhang D. Effects of L-carnitine against H2O2-induced oxidative stress in grass carp ovary cells (Ctenopharyngodon idellus).. Fish Physiol Biochem 2016 Jun;42(3):845-57.
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