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Veterinary journal (London, England : 1997)2013; 198(2); 472-478; doi: 10.1016/j.tvjl.2013.08.017

Expression of purinergic P2X receptor subtypes 1, 2, 3 and 7 in equine laminitis.

Abstract: Tissue sensitisation and chronic pain have been described in chronic-active laminitis in the horse, making treatment of such cases difficult. Purinergic P2X receptors are linked to chronic pain and inflammation. The aim of this study was to examine the expression of purinergic P2X receptor subtypes 1, 2, 3 and 7 in the hoof, palmar digital vessels and nerve, dorsal root ganglia and spinal cord in horses with chronic-active laminitis (n=5) compared to non-laminitic horses (n=5). Immunohistochemical analysis was performed on tissue sections using antibodies against P2X receptor subtypes 1-3 and 7. In horses with laminitis, there was a reduction in the thickness of the tunica media layer of the palmar digital vein as a proportion of the whole vessel diameter (0.48±0.05) compared to the non-laminitic group (0.57±0.04; P=0.02). P2X receptor subtype 3 was expressed in the smooth muscle layer (tunica media) of the palmar digital artery of horses with laminitis, but was absent in horses without laminitis. There was strong expression of P2X receptor subtype 7 in the proliferating, partially keratinised, epidermal cells of the secondary epidermal lamellae in the hooves of horses with laminitis, but no immunopositivity in horses without laminitis.
Publication Date: 2013-08-20 PubMed ID: 24080476DOI: 10.1016/j.tvjl.2013.08.017Google Scholar: Lookup
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  • Journal Article
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Summary

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The research investigates the expression of certain purinergic P2X receptors in horses with chronic-active laminitis, revealing variations in the expression of these receptors and changes in vein thickness in comparison with non-laminitic horses.

Research Objective and Methodology

  • The aim of the study was to examine the expression of purinergic P2X receptor subtypes 1, 2, 3, and 7 within various parts of the equine anatomy. This was done in an attempt to understand their role in chronic-active laminitis, a painful and difficult to treat condition in horses.
  • The researchers studied these receptors in the hoof, palmar digital vessels and nerves, dorsal root ganglia, and spinal cord of horses with chronic-active laminitis and compared the results with those of the non-laminitic horses.
  • A total of 5 laminitic and 5 control non-laminitic horses were included in the study.
  • The researchers used a technique called immunohistochemical analysis, using antibodies against P2X receptor subtypes 1-3 and 7. This method allowed the researchers to observe the presence of these P2X receptors within various tissues.

Results and Observations

  • In laminitic horses, the study found a reduction in the thickness of the tunica media layer of the palmar digital vein as a proportion of the whole vessel diameter. This implies changes in vascular properties that could be related to the disease mechanism in laminitis.
  • P2X receptor subtype 3 was expressed in the smooth muscle layer (tunica media) of the palmar digital artery of horses with laminitis but was absent in non-laminitic horses. This might contribute to the pathophysiology of the disease.
  • There was a strong expression of P2X receptor subtype 7 in proliferating, partially keratinised, epidermal cells of the secondary epidermal lamellae in the hooves of horses with laminitis but none in the horses without laminitis. This indicates that the changes in expression and localization of purinergic receptors might be a potential factor associated with the condition.

Significance of the study

  • The research suggests that chronic inflammation and pain experienced by horses with chronic-active laminitis might be due to changes in the purinergic P2X receptors and alterations in vascular properties.
  • Further investigation of these receptors could provide insight into the mechanisms of laminitis and might potentially lead to the development of more effective treatments for this debilitating condition in horses.

Cite This Article

APA
Zamboulis DE, Senior M, Clegg PD, Milner PI. (2013). Expression of purinergic P2X receptor subtypes 1, 2, 3 and 7 in equine laminitis. Vet J, 198(2), 472-478. https://doi.org/10.1016/j.tvjl.2013.08.017

Publication

ISSN: 1532-2971
NlmUniqueID: 9706281
Country: England
Language: English
Volume: 198
Issue: 2
Pages: 472-478
PII: S1090-0233(13)00392-4

Researcher Affiliations

Zamboulis, Danae E
  • Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, Leahurst Campus, Chester High Road, Neston, Cheshire CH64 7TE, UK.
Senior, Mark
    Clegg, Peter D
      Milner, Peter I

        MeSH Terms

        • Animals
        • Foot Diseases / genetics
        • Foot Diseases / metabolism
        • Foot Diseases / pathology
        • Foot Diseases / veterinary
        • Gene Expression Regulation
        • Horse Diseases / genetics
        • Horse Diseases / metabolism
        • Horse Diseases / pathology
        • Horses
        • Immunohistochemistry / veterinary
        • Organ Specificity
        • Receptors, Purinergic P2X / genetics
        • Receptors, Purinergic P2X / metabolism

        Citations

        This article has been cited 3 times.
        1. Daradics Z, Crecan CM, Rus MA, Morar IA, Mircean MV, Cătoi AF, Cecan AD, Cătoi C. Obesity-Related Metabolic Dysfunction in Dairy Cows and Horses: Comparison to Human Metabolic Syndrome. Life (Basel) 2021 Dec 16;11(12).
          doi: 10.3390/life11121406pubmed: 34947937google scholar: lookup
        2. Kharaz YA, Canty-Laird EG, Tew SR, Comerford EJ. Variations in internal structure, composition and protein distribution between intra- and extra-articular knee ligaments and tendons. J Anat 2018 Jun;232(6):943-955.
          doi: 10.1111/joa.12802pubmed: 29498035google scholar: lookup
        3. Zhao H, Yang BL, Liu ZX, Yu Q, Zhang WJ, Yuan K, Zeng HH, Zhu GC, Liu DM, Li Q. Microencapsulation improves inhibitory effects of transplanted olfactory ensheathing cells on pain after sciatic nerve injury. Neural Regen Res 2015 Aug;10(8):1332-7.
          doi: 10.4103/1673-5374.162769pubmed: 26487865google scholar: lookup