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Veterinary journal (London, England : 1997)2021; 270; 105626; doi: 10.1016/j.tvjl.2021.105626

The lipopolysaccharide model for the experimental induction of transient lameness and synovitis in Standardbred horses.

Abstract: An established lipopolysaccharide (LPS) model previously described in Warmbloods, was inconsistent in Standardbred horses, where lameness was not detected despite the presence of synovitis. The present study aimed to determine the dose of LPS from E. coli O55:B5 required to induce mild to moderate lameness following middle carpal joint injection in Standardbred horses and to quantitate the induced lameness over time, with and without anti-inflammatory pre-treatment. In a baseline trial, eight healthy, clinically sound Standardbred horses were used in a rule-based dose-escalation design trial, starting at a dose of 10 endotoxin units (EU). Lameness at trot was evaluated visually and quantitatively (using an inertial-sensor system and pressure plate analysis). Synovial fluid aspirates were analysed for total nucleated cell counts, total protein and prostaglandin E (PGE). Following 2 months wash-out, the effective LPS-dose determined in the baseline trial was used to evaluate the effect of anti-inflammatory treatment. A mixed model for repeated measures with horse as random effect was used for analysis. After injection of 10 EU LPS, the desired degree of lameness was observed in the baseline trial, with maximal lameness at post-injection hour (PIH) 4, followed by a rapid decline and return to baseline by PIH 48. No lameness was observed following pre-treatment with meloxicam. In synovial fluid, PGE was significantly higher at PIH 8 and PIH 24 in the baseline trial compared with following meloxicam pre-treatment. In conclusion, injection of the middle carpal joint with 10 EU LPS consistently induces a transient lameness and synovitis in Standardbred horses.
Publication Date: 2021-02-01 PubMed ID: 33641810DOI: 10.1016/j.tvjl.2021.105626Google Scholar: Lookup
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  • Journal Article

Summary

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This research examines the accuracy of a lipopolysaccharide (LPS) model to cause temporary lameness and joint inflammation in Standardbred horses, and it aims to establish the precise amount of LPS needed to induce such conditions. It also explores the timeline of the induced lameness and how it can be prevented through pre-treatment with anti-inflammatory drugs.

Objectives and Methodology of the Study

  • The study primarily sought to establish the exact dosage of LPS from a specific strain of E. coli (referred to as O55:B5) needed to cause mild to moderate lameness after being injected into a Standardbred horse’s middle carpal (a significant joint in a horse’s forelimb).
  • Eight healthy Standardbred horses were initially used in a structured trial that began with a dosage of 10 endotoxin units (EU) of LPS. The level of lameness was determined visually as well as quantitatively using advanced technology (an inertial sensor system and pressure plate analysis).
  • Besides observing lameness, the study also assessed the fluid within the horses’ joints for total cell counts, protein levels, and the presence of the inflammatory mediator named prostaglandin E (PGE).
  • After a two-month break, the same dose of LPS that proved effective in causing lameness was then used in an experiment to understand the effect of an anti-inflammatory drug called meloxicam. The analysis included repeated measurements and took into account the possible variation among individual horses.

Findings of the Study

  • At a dosage of 10 EU LPS, the desired level of lameness was achieved in the preliminary trial. The peak lameness occurred four hours after injection, followed by a rapid decline and eventual return to normalcy within 48 hours post-injection.
  • On the other hand, pre-treatment with meloxicam prevented any lameness after LPS injection.
  • The PGE levels were significantly higher at the eighth hour and 24th hour post-injection during the baseline trial compared to when horses were pre-treated with meloxicam.
  • In summary, injecting a Standardbred horse’s middle carpal joint with 10 EU LPS causes mild temporary lameness and joint inflammation. However, these outcomes can be mitigated if horses are pre-treated with meloxicam.

Cite This Article

APA
Van de Water E, Oosterlinck M, Korthagen NM, Duchateau L, Dumoulin M, van Weeren PR, Olijve J, van Doorn DA, Pille F. (2021). The lipopolysaccharide model for the experimental induction of transient lameness and synovitis in Standardbred horses. Vet J, 270, 105626. https://doi.org/10.1016/j.tvjl.2021.105626

Publication

ISSN: 1532-2971
NlmUniqueID: 9706281
Country: England
Language: English
Volume: 270
Pages: 105626
PII: S1090-0233(21)00021-6

Researcher Affiliations

Van de Water, E
  • Department of Surgery and Anaesthesiology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium. Electronic address: Eline.VandeWater@UGent.be.
Oosterlinck, M
  • Department of Surgery and Anaesthesiology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Korthagen, N M
  • Department of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 112, 3584 CM Utrecht, The Netherlands; Department of Orthopaedics, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands.
Duchateau, L
  • Biometrics Research Group, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Dumoulin, M
  • Department of Surgery and Anaesthesiology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
van Weeren, P R
  • Department of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 112, 3584 CM Utrecht, The Netherlands.
Olijve, J
  • Rousselot, Meulestedekaai 81, 9000 Gent, Belgium.
van Doorn, D A
  • Department of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 112, 3584 CM Utrecht, The Netherlands; Department of Farm Animal Health, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 7, 3584 CL Utrecht, The Netherlands; Equivado, Equine Nutrition Consultancy, Marnixlaan 80, 3552 HG Utrecht, The Netherlands.
Pille, F
  • Department of Surgery and Anaesthesiology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.

MeSH Terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
  • Carpal Joints / drug effects
  • Dinoprostone / analysis
  • Disease Models, Animal
  • Escherichia coli
  • Horse Diseases / etiology
  • Horse Diseases / prevention & control
  • Horses
  • Injections, Intra-Articular
  • Lameness, Animal / etiology
  • Lameness, Animal / prevention & control
  • Lipopolysaccharides / administration & dosage
  • Meloxicam / administration & dosage
  • Synovial Fluid / chemistry
  • Synovitis / etiology
  • Synovitis / prevention & control
  • Synovitis / veterinary

Citations

This article has been cited 4 times.
  1. Maldonado MD, Parkinson SD, Story MR, Haussler KK. The Effect of Chiropractic Treatment on Limb Lameness and Concurrent Axial Skeleton Pain and Dysfunction in Horses.. Animals (Basel) 2022 Oct 19;12(20).
    doi: 10.3390/ani12202845pubmed: 36290230google scholar: lookup
  2. Ask K, Andersen PH, Tamminen LM, Rhodin M, Hernlund E. Performance of four equine pain scales and their association to movement asymmetry in horses with induced orthopedic pain.. Front Vet Sci 2022;9:938022.
    doi: 10.3389/fvets.2022.938022pubmed: 36032285google scholar: lookup
  3. Broomé S, Ask K, Rashid-Engström M, Haubro Andersen P, Kjellström H. Sharing pain: Using pain domain transfer for video recognition of low grade orthopedic pain in horses.. PLoS One 2022;17(3):e0263854.
    doi: 10.1371/journal.pone.0263854pubmed: 35245288google scholar: lookup
  4. Andersen PH, Broomé S, Rashid M, Lundblad J, Ask K, Li Z, Hernlund E, Rhodin M, Kjellström H. Towards Machine Recognition of Facial Expressions of Pain in Horses.. Animals (Basel) 2021 Jun 1;11(6).
    doi: 10.3390/ani11061643pubmed: 34206077google scholar: lookup