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Local hemodynamics, permeability, and oxygen metabolism during acute inflammation of innervated or denervated isolated equine joints.

Abstract: To determine oxygen metabolism, permeability, and blood flow in isolated joints in response to interleukin 1beta (IL-1beta) and contribution of innervation. Methods: One metacarpophalangeal (MCP) joint of 24 adult horses. Methods: The MCP joint was isolated for 6 hours in a pump-perfused, auto-oxygenated, innervated or denervated preparation. Isolated joints were assigned to the following 4 groups: control, control-denervated, inflamed, and inflamed-denervated, and inflammation was induced by intra-articular injection of IL-1beta. Circuit arterial and venous pressures, flows, and blood gas tensions, synovial fluid production, and intra-articular pressure were measured. Total vascular resistance; oxygen delivery, consumption, and extraction ratio (ER); and permeability surface area product were calculated. Synovial membrane blood flow was determined at 0, 60, and 330 minutes. Synovial membrane wet-to-dry ratio was obtained, and permeability to macromolecules was determined by intra-articular injection of Evans blue albumin and fluorescein isothiocyanate-conjugated dextran. Results: Oxygen delivery and synovial membrane blood flow progressively increased but were not different among groups. Oxygen consumption and ER significantly increased in inflamed joints, as did intraarticular pressure and synovial fluid production. Inflamed joints had greater wet-to-dry ratio. Albumin permeability significantly increased in the villous synovial membrane of the inflamed groups, and dextran permeability was increased in the innervated groups, with a trend toward increased permeability in inflamed groups. Conclusions: Inflammation significantly increased oxygen demand, which was initially met by increased ER. Permeability to small molecules was increased with inflammation; innervation increased permeability to large molecules. Use of an isolated joint model enabled documentation of the physiologic responses of the joint to acute inflammation.
Publication Date: 1998-10-22 PubMed ID: 9781467
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research paper attempts to understand the effects of acute inflammation on equine joints, specifically focusing on oxygen metabolism, permeability, and blood flow. The study conducted various measurements and procedures on isolated horse joint groups exposed to inflammation under different conditions.

Research Methodology

  • The study focused on the metacarpophalangeal (MCP) joint of 24 adult horses. The MCP joint was isolated and kept under pump-perfused, auto-oxygenated preparation for 6 hours. Some joints were denervated, i.e., deprived of nerve supply.
  • The isolated joints were categorized into four groups — control, control-denervated, inflamed, and inflamed-denervated for the experiment. The inflammation in the joint was induced by the intra-articular injection of Interleukin 1beta (IL-1beta), a protein involved in inflammatory response.
  • Several measurements were taken and calculations executed. This included blood pressures, flows, and gas tensions, intra-articular pressure, synovial fluid production, oxygen delivery, consumption, and extraction ratio (ER), amongst others.
  • The permeability of the joints to macromolecules was obtained by injecting Evans blue albumin and fluorescein isothiocyanate-conjugated dextran into the joint.

Research Findings

  • The study discovered that oxygen delivery and synovial membrane blood flow gradually increased across all groups. While the oxygen consumption and ER significantly rose in inflamed joints, as did the intra-articular pressure and synovial fluid production.
  • Inflamed joints exhibited a higher wet-to-dry ratio, implying they held more fluid than their control counterparts. Additionally, the villous synovial membrane of the inflamed groups had significantly increased permeability to albumin, a protein molecule.
  • Dextran permeability increased in innervated groups, with a similar trend noticed in inflamed groups, but this change was not significant. It can be concluded from these findings that inflammation increases permeability to small molecules, while innervation increases permeability to large molecules.

Conclusion

  • The study concluded that inflammation significantly increased oxygen demand, which was initially met by an increased extraction ratio. The experiments confirmed that acute inflammation impacts the physiology of the equine joint, altering its oxygen metabolism, blood flow, and permeability.
  • Overall, the research emphasized the importance of understanding these physiologic responses during inflammation, providing valuable insights for potential therapeutic approaches to inflammatory joint conditions in animals.

Cite This Article

APA
Hardy J, Bertone AL, Muir WW. (1998). Local hemodynamics, permeability, and oxygen metabolism during acute inflammation of innervated or denervated isolated equine joints. Am J Vet Res, 59(10), 1307-1316.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 59
Issue: 10
Pages: 1307-1316

Researcher Affiliations

Hardy, J
  • Department of Veterinary Clinical Sciences, The Ohio State University, Columbus 43210, USA.
Bertone, A L
    Muir, W W

      MeSH Terms

      • Albumins / metabolism
      • Animals
      • Arthritis / metabolism
      • Arthritis / veterinary
      • Denervation / veterinary
      • Dextrans / metabolism
      • Female
      • Fluorescein-5-isothiocyanate / analogs & derivatives
      • Fluorescein-5-isothiocyanate / metabolism
      • Hemodynamics
      • Horse Diseases / metabolism
      • Horses
      • In Vitro Techniques
      • Joints / blood supply
      • Joints / innervation
      • Joints / metabolism
      • Male
      • Oxygen / metabolism
      • Permeability
      • Random Allocation
      • Regional Blood Flow
      • Synovial Fluid / metabolism
      • Synovial Membrane / blood supply
      • Synovial Membrane / innervation
      • Synovial Membrane / metabolism