Animal models of acute joint injury are useful for study of changes in joint tissues that may eventually lead to degradative disease. Our laboratory has developed a joint trauma model using a single blunt impact to the patellofemoral joint of rabbits and documented softening of retro-patellar cartilage and thickening of its underlying bone out to 12 months post-trauma. In the present study, we examined changes in these joint tissues out to 36 months post-impact. Forty-nine Flemish giant rabbits were impacted on the right patellofemoral joint and sacrificed at one of six times: 0, 4.5, 7.5, 12, 24, and 36 months post-impact. A 30% reduction in the compressive modulus of traumatized retro-patellar cartilage occurred at 4.5 months versus the contralateral, non-impacted limb and remained at this reduced level out to 36 months. The fluid permeability of traumatized cartilage also increased over time from baseline and versus the non-impacted limb. Tissue thickness increased slightly at 4.5 months and then decreased over time to a 45% difference from baseline at 36 months post-trauma. While impacted cartilage revealed a significantly greater length of surface fissuring than contralateral, non-impacted cartilage, no time-dependent changes were evident in this study. Moreover, the number and depth of these impact surface lesions did not change as a function of time. Finally, the histological analyses indicated that the thickness of underlying subchondral bone increased over time from baseline and versus that in the non-impacted limb. This long-term study suggested an association between a decrease in the characteristic time constant of traumatized cartilage and thickening of the underlying subchondral bone. Any potential cause and effect relationship, however, must be investigated in future studies.
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http://dx.doi.org/10.1016/S0736-0266(01)00135-8 | DOI Listing |
PLoS One
December 2013
Stems Medical Clinic, Seoul, Republic of Korea.
Mesenchymal stem cells from several sources (bone marrow, synovial tissue, cord blood, and adipose tissue) can differentiate into variable parts (bones, cartilage, muscle, and adipose tissue), representing a promising new therapy in regenerative medicine. In animal models, mesenchymal stem cells have been used successfully to regenerate cartilage and bones. However, there have been no follow-up studies on humans treated with adipose-tissue-derived stem cells (ADSCs) for the chondromalacia patellae.
View Article and Find Full Text PDFOsteoarthritis Cartilage
September 2009
Human Performance Laboratory, Faculty of Kinesiology, University of Calgary, AB, Canada.
Objective: The objective of this study was to investigate the effects of botulinum toxin type-A (BTX-A) induced quadriceps weakness on micro-structural changes in knee cartilage of New Zealand White (NZW) rabbits.
Design: Fifteen rabbits were divided randomly into an experimental and a sham control group. Each group received a unilateral single quadriceps muscle injection either with saline (sham control; n=4) or BTX-A (experimental; n=11).
Arch Orthop Trauma Surg
July 2009
Institute of Orthopaedic Research an Biomechanics, University of Ulm, Helmholtzstrasse 14, 89081, Ulm, Germany.
Introduction: Experimental studies on metaphyseal fractures are rare and do not control the biomechanical conditions in the healing zone. This study aimed to develop an improved experimental model, which characterizes and controls the biomechanical condition in the fracture gap of a metaphyseal fracture.
Materials And Methods: A partial osteotomy model in the distal femur of the sheep was developed.
J Orthop Res
November 2005
Orthopaedic Biomechanics Laboratories, College of Osteopathic Medicine, Michigan State University, A414 East Fee Hall, East Lansing, MI 48824, USA.
We have previously shown that surface lesions and acute necrosis of chondrocytes are produced by severe levels of blunt mechanical load, generating contact pressures greater than 25 MPa, on chondral and osteochondral explants. We have also found surface lesions and chronic degradation of retro-patellar cartilage within 3 years following a 6J impact intensity with an associated average pressure of 25 MPa in the rabbit patello-femoral joint. We now hypothesized that cellular necrosis is produced acutely in the retro-patellar cartilage in this model as a result of a 6J impact and that an early injection of the non-ionic surfactant, poloxamer 188 (P188), would significantly reduce the percentage of necrotic cells in the traumatized cartilage.
View Article and Find Full Text PDFJ Biomech
May 2005
Orthopaedic Biomechanics Laboratories, College of Osteopathic Medicine, Michigan State University, A414 East Fee Hall, East Lansing, Michigan 48824, USA.
Our laboratory has developed an animal model to study factors leading to chronic disease in a blunt impacted joint. Studies to date indicate post trauma softening of the impacted joint cartilage, but a limited degree of histological degradation in the tissue. The model utilizes treadmill exercise of the animal post trauma.
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