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Effects of short-term cast immobilization on equine articular cartilage.

Abstract: Hexosamine concentration (an index of proteoglycan content), DNA content (an index of cellularity), and [35S]sulfate incorporation (an index of proteoglycan synthesis) of articular cartilage were measured in biopsy specimens from medial proximal sesamoid bone, medial condyle of the third metacarpal bone, and proximal dorsal rim of the proximal phalanx in both metacarpophalangeal joints of 6 adult horses. One limb was then placed in a fiberglass cast that extended down from the proximal portion of the metacarpus and enclosed the hoof; the other limb was not casted. After 30 days of stall confinement, additional specimens were taken from the medial proximal sesamoid bone, medial condyle of the third metacarpal bone, midproximal portion of the proximal phalanx, distal portion of the proximal phalanx, and proximal portion of the middle phalanx of both limbs for comparison. Immobilization resulted in an apparent decrease in the hexosamine content of the cartilage when the 30-day immobilized vs 30-day mobilized specimens were analyzed. This decrease was accentuated by opposing trends in the 2 limbs. The immobilized cartilage tended to lose hexosamine, whereas the mobilized limb tended to gain hexosamine during the 30-day period; a similar trend also was seen with [35S] incorporation, but this trend was not statistically significant. The largest change was a significant increase in glycosaminoglycan synthesis in the mobilized limb, compared with little change in the immobilized joint cartilage. We concluded that contralateral limbs are unsuitable for controls in immobilization studies because of their biological response to increased weight bearing.(ABSTRACT TRUNCATED AT 250 WORDS)
Publication Date: 1993-03-01 PubMed ID: 8498752
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research examined the impact of short-term immobilization of horse limbs via a cast on the articular cartilage, observing a decrease in hexosamine content in immobilized limbs, contrasted with an increase in mobilized limbs over a 30-day period.

Research Scope and Procedure

The study was conducted on six adult horses. Biopsies of articular cartilage were taken from specified regions in both metacarpophalangeal joints of each horse. Hexosamine concentration, DNA content, and [35S]sulfate incorporation were measured as indices of proteoglycan content, cellularity, and proteoglycan synthesis, respectively. Thereafter, one limb of each horse was immobilized using a fiberglass cast while the other was left free. After a 30-day period of stall confinement, additional specimens were collected from both limbs of each horse for comparison.

Findings and Results

  • The immobilized horse limbs displayed a notable decrease in articular cartilage hexosamine content when compared with the free limbs.
  • This trend was further accentuated by an inconsistent trend in the two limbs, where the immobilized limb lost hexosamine while the free limb gained an increased amount of hexosamine within the 30-day period.
  • Similar trends were identified with [35S] incorporation, though these were not significantly conclusive.
  • Another key finding was the major increase in the synthesis of glycosaminoglycan in the free horse limb as opposed to minimal change in the immobilized horse limb.

Conclusions

The study concluded that contralateral limbs (i.e., opposing limbs of the body) are unsuitable as control constituents in immobilization studies given their biological response to increased weight-bearing. In simpler terms, if one limb is immobilized, the opposite limb tends to endure more weight, thus altering its physiological mechanisms, including those of the articular cartilage.

Cite This Article

APA
Richardson DW, Clark CC. (1993). Effects of short-term cast immobilization on equine articular cartilage. Am J Vet Res, 54(3), 449-453.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 54
Issue: 3
Pages: 449-453

Researcher Affiliations

Richardson, D W
  • Department of Clinical Studies, School of Veterinary Medicine, University of Pennsylvania, New Bolton Center, Kennett Square 19348.
Clark, C C

    MeSH Terms

    • Animals
    • Cartilage, Articular / metabolism
    • Casts, Surgical / veterinary
    • DNA / analysis
    • DNA / metabolism
    • Hexosamines / metabolism
    • Horses
    • Immobilization
    • Proteoglycans / analysis
    • Proteoglycans / biosynthesis
    • Proteoglycans / metabolism
    • Reference Values
    • Sulfates / metabolism
    • Sulfur Radioisotopes

    Citations

    This article has been cited 5 times.
    1. Bertoni L, Jacquet-Guibon S, Branly T, Legendre F, Desancé M, Mespoulhes C, Melin M, Hartmann DJ, Schmutz A, Denoix JM, Galéra P, Demoor M, Audigié F. An experimentally induced osteoarthritis model in horses performed on both metacarpophalangeal and metatarsophalangeal joints: Technical, clinical, imaging, biochemical, macroscopic and microscopic characterization. PLoS One 2020;15(6):e0235251.
      doi: 10.1371/journal.pone.0235251pubmed: 32584901google scholar: lookup
    2. Maninchedda U, Lepage OM, Gangl M, Hilairet S, Remandet B, Meot F, Penarier G, Segard E, Cortez P, Jorgensen C, Steinberg R. Development of an equine groove model to induce metacarpophalangeal osteoarthritis: a pilot study on 6 horses. PLoS One 2015;10(2):e0115089.
      doi: 10.1371/journal.pone.0115089pubmed: 25680102google scholar: lookup
    3. McIlwraith CW, Frisbie DD, Kawcak CE. The horse as a model of naturally occurring osteoarthritis. Bone Joint Res 2012 Nov;1(11):297-309.
      doi: 10.1302/2046-3758.111.2000132pubmed: 23610661google scholar: lookup
    4. Gregory MH, Capito N, Kuroki K, Stoker AM, Cook JL, Sherman SL. A review of translational animal models for knee osteoarthritis. Arthritis 2012;2012:764621.
      doi: 10.1155/2012/764621pubmed: 23326663google scholar: lookup
    5. Firth EC. The response of bone, articular cartilage and tendon to exercise in the horse. J Anat 2006 Apr;208(4):513-26.