Role of oxidative tissue injury in the pathophysiology of experimentally induced equine laminitis: a comparison of 2 models.
Abstract: Oxidative stress reportedly plays a role in sepsis-induced organ dysfunction and failure in many species. In septic horses, laminae are targeted; evidence of laminar oxidative stress has been reported experimentally in the black walnut extract (BWE) model. Carbohydrate (CHO)-induced laminitis may be more similar to clinical sepsis-related laminitis than the BWE model in that animals with CHO-induced disease commonly develop laminar failure. The role of oxidative stress in the CHO model remains unknown. Objective: Markers of oxidative stress will be increased in laminae from horses with BWE- and CHO-induced laminitis. Methods: Banked laminar tissue from various time points from animals subjected to BWE (n = 15) and CHO (n = 20) protocols. Methods: Laminar 4-hydroxynonenal (4-HNE) and protein carbonyl content were evaluated by slot blot analysis. Laminar 3-nitrotyrosine (3-NT) immunohistochemistry was performed. Results: The number of laminar 3-NT (+) cells was increased at developmental and Obel grade 1 (OG1) time points in the BWE model (versus control [CON]; P= .013) and lower in OG1 tissues than CON in the CHO model (P = .04). No change in 4-HNE content was observed in the CHO model, and no increase in laminar protein carbonyl content was present in either model (P > .05). Conclusions: These results do not support a prominent role for oxidative stress at examined time points in CHO-overload laminitis and support transient oxidative stress in the BWE model. Tissue oxidation does not appear to be a central early pathophysiologic event in CHO-associated laminitis.
Copyright © 2011 by the American College of Veterinary Internal Medicine.
Publication Date: 2011-03-21 PubMed ID: 21418321DOI: 10.1111/j.1939-1676.2011.0706.xGoogle Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research explored the role of oxidative stress in the development of equine laminitis, a painful and potentially life-threatening condition in horses, using two models: the black walnut extract (BWE) model and the carbohydrate (CHO)-induced model. The results suggest that oxidative stress might play a minor role in the BWE model but not a significant role in the disease’s progress when it is CHO-induced.
Research Background
- The condition under study, equine laminitis, is a serious disorder impacting horses. It results in intense pain and lameness due to inflammation of the laminae, which are connective tissues in the horse’s hoof.
- Previous studies have suggested a role for oxidative stress in equine laminitis, particularly in cases induced by sepsis, a systemic inflammatory response to infection. Oxidative stress results from an imbalance between the production of reactive oxygen species (free radicals) and the body’s ability to counteract their harmful effects.
- Using two different models – the black walnut extract (BWE) model and the carbohydrate (CHO)-induced model – this study aimed to further investigate the role of oxidative stress in laminitis.
Methodology
- The researchers used banked laminar tissue samples from animals who had been subjected to either BWE (n = 15) or CHO (n = 20) protocols, meaning these animals were exposed to either BWE or an excess of carbohydrates to induce laminitis.
- They then evaluated the presence of markers of oxidative stress in these tissues. Specifically, they measured the content of 4-hydroxynonenal (4-HNE) and protein carbonyl, both of which increase under oxidative stress.
- They also performed immunohistochemistry for 3-nitrotyrosine (3-NT), another marker of oxidative stress.
Results
- The results showed an increase in 3-NT positive cells in the BWE model at developmental time points and early-stage laminitis (Obel grade 1), when compared to control samples.
- In contrast, 3-NT cell numbers were lower in the CHO model than in the control.
- No change was observed in 4-HNE content in the CHO model, and no increase in protein carbonyl content was seen in either model.
Conclusions
- The findings suggest that oxidative stress may play a transient role in early-stage laminitis in the BWE model but does not seem to be a major factor in the CHO model.
- The researchers concluded that tissue oxidation does not appear to be a central early pathophysiological event in laminitis associated with an overload of carbohydrates.
Cite This Article
APA
Burns TA, Westerman T, Nuovo GJ, Watts MR, Pettigrew A, Yin C, Belknap JK.
(2011).
Role of oxidative tissue injury in the pathophysiology of experimentally induced equine laminitis: a comparison of 2 models.
J Vet Intern Med, 25(3), 540-548.
https://doi.org/10.1111/j.1939-1676.2011.0706.x Publication
Researcher Affiliations
- Ohio State University College of Veterinary Medicine, Columbus, OH 43210, USA.
MeSH Terms
- Aldehydes / analysis
- Aldehydes / metabolism
- Animals
- Biomarkers
- Disease Models, Animal
- Foot Diseases / chemically induced
- Foot Diseases / metabolism
- Foot Diseases / physiopathology
- Foot Diseases / veterinary
- Hoof and Claw / drug effects
- Horse Diseases / chemically induced
- Horse Diseases / metabolism
- Horse Diseases / physiopathology
- Horses
- Inflammation / chemically induced
- Inflammation / physiopathology
- Inflammation / veterinary
- Juglans / chemistry
- Lipid Peroxidation
- Oxidative Stress / physiology
- Plant Extracts / chemistry
- Plant Extracts / toxicity
- Proteins / metabolism
- Reactive Nitrogen Species
- Reactive Oxygen Species
- Starch / administration & dosage
- Starch / toxicity
- Tyrosine / metabolism
Citations
This article has been cited 2 times.- Celi P, Gabai G. Oxidant/Antioxidant Balance in Animal Nutrition and Health: The Role of Protein Oxidation. Front Vet Sci 2015;2:48.
- Burns TA, Watts MR, Weber PS, McCutcheon LJ, Geor RJ, Belknap JK. Effect of dietary nonstructural carbohydrate content on activation of 5'-adenosine monophosphate-activated protein kinase in liver, skeletal muscle, and digital laminae of lean and obese ponies. J Vet Intern Med 2014 Jul-Aug;28(4):1280-8.
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