Laminar xanthine oxidase, superoxide dismutase and catalase activities in the prodromal stage of black-walnut induced equine laminitis.
Abstract: REASONS FOR STUDY: Xanthine oxidase (XO)-dependent production of superoxide anion and hydrogen peroxide, a characteristic of ischaemia-reperfusion injury, may contribute to the development of equine laminitis. Objective: To determine the levels of XO and antioxidant enzymes (catalase, superoxide dismutase [SOD]) in the digital laminae of normal horses (CON) and horses in the developmental stage of laminitis using the black walnut extract (BWE) model. Methods: Healthy horses (n = 12) were administered BWE (BWE group, n = 6), or water (CON group, n = 6) through a nasogastric tube. At the onset of leucopenia in the BWE-treated animals, all horses were anaesthetised, digital laminae and other samples collected rapidly and flash frozen, and the animals subjected to euthanasia. Extracts of the frozen tissues were assayed for the 2 conformational forms of xanthine: oxygen oxidoreductase (XOR), namely, xanthine dehydrogenase (XDH) and xanthine oxidase (XO), as well as the antioxidant enzymes, SOD and catalase. Results: Extracts of liver, lungs and skin, but not digital laminae, from either CON or BWE-treated horses had endogenous SOD, whereas all had endogenous XO and catalase. The levels of XDH, XO and catalase were similar in extracts of laminae from CON and BWE-treated horses as was the ratio of XDH to XO in extracts. Conclusions: The absence of increased XO activity suggest against the involvement of this reactive oxygen intermediate-generating system in the development of laminar pathology in BWE-treated horses. Conversely, the absence of SOD from extracts of equine digital laminae, but not other tissues, suggests that the equine digital laminae are highly susceptible to damage by superoxide anion, produced, for example, by emigrant inflammatory leucocytes.
Publication Date: 2007-01-19 PubMed ID: 17228595DOI: 10.2746/042516406x151320Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Research Support
- U.S. Gov't
- Non-P.H.S.
Summary
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The research paper in question investigates if xanthine oxidase (XO)-dependent production of harmful substances contributes to the development of equine laminitis, a painful disease in horses. The study further includes examining levels of antioxidant enzymes in horses, both normal and those in a developmental stage of laminitis induced via black walnut extract.
Research Motivation
- The study was inspired by the hypothesis that XO, an enzyme that produces potentially damaging substances like superoxide anion and hydrogen peroxide (common in ischaemia-reperfusion injury), might contribute to the development of equine laminitis.
- The objective was to monitor levels of XO and antioxidative enzymes (such as catalase and superoxide dismutase [SOD]) in the digital laminae (thin flat structures in hooves) of both healthy horses and those going through the early stages of laminitis.
Methodology
- The research involved giving black walnut extract (BWE) to half of twelve healthy horses, inducing a state similar to initial stages of laminitis. A control group received water only.
- When leukopenia (a decrease in white blood cell count) occurred in BWE-administered horses, samples from digital laminae and other tissues were collected from all horses and promptly flash-frozen for preservation. Subsequently, the horses were humanely euthanized.
- The research team then examined the frozen samples for the two types of xanthine: oxygen oxidoreductase (XOR) – xanthine dehydrogenase (XDH) and xanthine oxidase (XO), and antioxidant enzymes, SOD and catalase.
Findings
- They found that XO and catalase were present in all samples, while SOD was only found in liver, lungs, and skin but not in digital laminae, regardless of whether the horse had been treated with BWE or was part of the control group.
- The levels of XDH, XO, and catalase in the digital laminae samples showed no significant discrepancy between the BWE-treated horses and the control group. Additionally, the ratio of XDH to XO was also consistent across the extracts.
Conclusions
- Based on their results, the researchers inferred that XO activity did not increase in this early stage of disease, suggesting it may not contribute to laminitis’ development.
- However, the researchers suggested that the lack of SOD in equine digital laminae could potentially make it more prone to damage by superoxide anion. This might occur as part of an inflammatory response with white blood cells migrating to the site of injury or infection.
Cite This Article
APA
Loftus JP, Belknap JK, Stankiewicz KM, Black SJ.
(2007).
Laminar xanthine oxidase, superoxide dismutase and catalase activities in the prodromal stage of black-walnut induced equine laminitis.
Equine Vet J, 39(1), 48-53.
https://doi.org/10.2746/042516406x151320 Publication
Researcher Affiliations
- Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts 01003, USA.
MeSH Terms
- Animals
- Catalase / metabolism
- Female
- Foot Diseases / enzymology
- Foot Diseases / immunology
- Hoof and Claw
- Horse Diseases / enzymology
- Horse Diseases / immunology
- Horses
- Hydrogen Peroxide / metabolism
- Juglans / chemistry
- Lameness, Animal / enzymology
- Lameness, Animal / immunology
- Male
- Plant Extracts / adverse effects
- Superoxide Dismutase / metabolism
- Xanthine Oxidase / metabolism
Citations
This article has been cited 5 times.- Storms N, Medina Torres C, Franck T, Sole Guitart A, de la Rebière G, Serteyn D. Presence of Myeloperoxidase in Lamellar Tissue of Horses Induced by an Euglycemic Hyperinsulinemic Clamp. Front Vet Sci 2022;9:846835.
- Leise BS, Watts MR, Roy S, Yilmaz AS, Alder H, Belknap JK. Use of laser capture microdissection for the assessment of equine lamellar basal epithelial cell signalling in the early stages of laminitis. Equine Vet J 2015 Jul;47(4):478-88.
- Coyne MJ, Cousin H, Loftus JP, Johnson PJ, Belknap JK, Gradil CM, Black SJ, Alfandari D. Cloning and expression of ADAM-related metalloproteases in equine laminitis. Vet Immunol Immunopathol 2009 Jun 15;129(3-4):231-41.
- Serteyn D, Storms N, Mouithys-Mickalad A, Sandersen C, Niesten A, Duysens J, Graide H, Ceusters J, Franck T. Revealing the Therapeutic Potential of Muscle-Derived Mesenchymal Stem/Stromal Cells: An In Vitro Model for Equine Laminitis Based on Activated Neutrophils, Anoxia-Reoxygenation, and Myeloperoxidase. Animals (Basel) 2024 Sep 14;14(18).
- Cocco R, Sechi S, Rizzo M, Arrigo F, Giannetto C, Piccione G, Arfuso F. Assessing the Peripheral Levels of the Neurotransmitters Noradrenaline, Dopamine and Serotonin and the Oxidant/Antioxidant Equilibrium in Circus Horses. Animals (Basel) 2024 Aug 14;14(16).
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