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PubMed1986

Effects of exposure to ambient air on articular cartilage of rabbits.

Effects of exposure to ambient air (20 to 22 C) on articular cartilage from rabbits were evaluated. Bilateral arthrotomies were performed on the stifles of 18 New Zealand White rabbits. The cranial surface of the left distal femur, including the articular cartilage of the trochlea, was exposed to air for 2 hours. The right stifle was opened and closed immediately. Six rabbits were killed at the end of the surgical operation (group 1), 6 after 2 weeks (group 2), and 6 after 4 weeks (group 3), and femurs were harvested. A distinct color change was seen in the exposed cartilage in group 1; however, minimal change was detected in group 2, and no change was seen in group 3. Proteoglycan content did not differ between the exposed and control cartilage in any group. The number of viable cells and empty lacunae in articular cartilage did not differ between the exposed and control femurs. Total cell counts and degenerative cell counts were similar, comparing the left and right trochlea in groups 1 and 3. A significant increase in cellularity was noticed in the radial zone of the exposed cartilage in group 2 (P less than 0.01). In the same group, a significantly increased number of degenerative cells were seen in the tangential zone of the exposed cartilage (P less than 0.05). Changes in cellularity were consistent with cartilage damage. Seemingly, exposing articular cartilage to air for 2 hours causes reversible cartilage damage.

Air↗
PubMed1983

Investigational approaches to articular cartilage preservation.

A brief review of articular cartilage preservation identifies several directions and concerns for modern investigators. First, storage of intact cartilage in such solutions as alcohol, merthiolate, plasma, and saline may not be as good as storage in air. Second, viable cartilage appears to fare better than nonviable cartilage after transplantation. Third, freezing of isolated cartilage cells appears to be a satisfactory method for preserving viability, but the same may not be true for cartilage tissue slices, slivers, or explants. Fourth, tissue culture of slices seems to provide excellent preservation of cells in their matrix. Fifth, freezing of intact cartilage presents problems of water diffusion, as well as penetration of cryopreservative. Extremely slow freezing may provide an answer to these problems. Sixth, transplantation of isolated chondrocytes into cartilage defects does not seem to provide regeneration of articular cartilage, but transplantation of slices or larger pieces may restore a more normal appearance to the joint surface. Further investigation is obviously necessary and should continue to provide information and knowledge toward the goal of successful preservation of functional articular cartilage.

Animals↗
PubMed1980

[Growth hormone: mode of action on different varieties of cartilage (author's transl)].

1) The growth of epiphyseal cartilages of long bones, of spheno-occipital synchondrosis of the cranial base, of the cartilage of the nasal septum, of lateral cartilaginous masses of the ethmoid, of cartilage between body and greater wings of the sphenoid (all stemming from the primary cartilaginous skeleton of the organism), is subject to general extrinsic factors and, more specifically, to the growth hormone (STH) and somatomedin. In this case, orthopedic devices can alterate the direction but not the amount of growth. 2) The growth of condylar, coronoid and angular cartilages of the mandible, of the cartilage of the midpalatal suture, and of the cartilage in some cranial sutures (all of secondary formation during phylogenesis and ontogenesis) is subject to local extrinsic factors as well as to growth hormone and somatomedin. In this case, appropriate orthopedic devices may modulate both the direction and the amount of growth. 3) Our cybernetic models attempt to account for the mechanisms of facial growth. By intensifying the forward growth of the nasal septum cartilage, the STH and somatomedin stimulate the forward growth of the upper jaw, i.e. the forward positioning of the superior dental arch (the position of which is the "constantly changing reference input" of the servosystem). The "operation of confrontation" between the position of the upper and lower occlusal surfaces (the position of the lower dental arch is the "controlled variable" of the servosystem) gives then rise to a "deviation signal" (originating from detectors of occlusal adjustment) whose "reduction" is made possible by a supplementary postural activity of the lateral pterygoid muscle resulting, extemporaneously, in an appropriate forward positioning of the mandible and, with time, in a supplementary growth of the condylar cartilage. By intensifying the outward growth of lateral cartilaginous masses of the ethmoid and of the cartilage between the body and greater wings of the sphenoid, the STH and somatomedin bring about a lateralization of both the left and right sides of the upper jaw and, in this way, stimulate the growth of the secondary cartilage of the midpalatal suture.

Animals↗
PubMed1994

Excess of metalloproteases over tissue inhibitor of metalloprotease may contribute to cartilage degradation in osteoarthritis and rheumatoid arthritis.

BACKGROUND: In an attempt to identify the factor(s) involved in the modulation of the degradative pathway of articular cartilage, we previously reported a possible imbalance between the levels of biologically active forms of metalloproteases and tissue inhibitor of metalloprotease (TIMP) in osteoarthritis (OA) cartilage. EXPERIMENTAL DESIGN: We extended our analysis on the protein level and the synthesis of stromelysin-1, collagenase, TIMP-1, and TIMP-2 in normal, OA, and RA cartilages, and provided information on the synthesis pattern of these proteins in respect to the action of interleukin-1 (IL-1). These protein concentrations were determined by specific sandwich EIA assays. RESULTS: This study allowed us to establish that the concentration of stromelysin-1 and collagenase is elevated in both OA and rheumatoid arthritis (RA) cartilages when compared with normal, with significantly higher levels of collagenase found in OA (p < 0.0003) and RA (p < 0.0001), and of stromelysin-1 in RA (p < 0.02). In all cases, the level of stromelysin-1 significantly exceeded (a few 100-fold) the collagenase level. The cartilage TIMP-1 level was notably enhanced only in RA, whereas TIMP-2 was increased in both OA and RA cartilage. RA patients with active disease had a higher level of metalloproteases and TIMP than those patients with inactive disease. Moreover, patients taking steroids alone or in combination with methotrexate had a markedly lower metalloprotease level without any changes in the TIMP-1 level. In culture cartilage explants, the synthesis of stromelysin-1 was enhanced in RA cartilage, whereas the level of collagenase was increased both in OA and RA explants. When compared with normal patients, the TIMP-1 synthesis was essentially unchanged in arthritic explants, whereas the level of TIMP-2 was decreased in RA explants when compared to OA. IL-1 induced a statistically significant increased synthesis of metalloproteases with the highest level found in arthritic explants. IL-1 also significantly decreased the TIMP-1 synthesis in OA and RA explants, and the TIMP-2 synthesis in OA. CONCLUSIONS: This study demonstrates that stromelysin-1 is the predominant metalloprotease synthesized in human articular cartilage and that both TIMP-1 and TIMP-2 are present in this tissue. The differential regulation of metalloprotease and TIMP syntheses by IL-1 suggests that this cytokine, during inflammatory conditions, may promote cartilage degradation by creating an imbalance between the level of these enzymes and their inhibitors.

Aged↗
PubMed1993

Cartilage warping: an experimental model.

Cadaveric cartilage was cut into blocks with a newly devised cartilage cutter. Over one-hundred pieces of cartilage were used to define a kinetics curve of cartilage warping. Kinetics curves were developed for a control group of cartilage blocks placed in saline-soaked gauze (n = 46). In addition, kinetics curves were developed for cartilage placed in hypotonic saline (n = 14), hypertonic saline (n = 14), and cyanoacrylate glue (n = 6). Photographs of all groups were taken at timed intervals in order to plot the cartilage warping. It was found that pieces of cartilage which were cut peripherally (n = 6) warped twice as much as those cut centrally (n = 40). This was significant to p = 0.001. Within 15 minutes, centrally cut pieces of cartilage warped to approximately 90 percent of their end warpage; on the other hand, peripherally cut pieces of cartilage required 30 minutes to warp 90 percent of their destined warpage. The variables used did not significantly alter the kinetics curves as compared with control.

Cadaver↗
PubMed1995

[Changes in the visco-elastic properties of the articular cartilage incubated in various kinds of liquid].

The purpose of our experiment was to investigate the way in which the visco-elastic properties of the articular cartilage of a loading joint responded to various liquid environments. Using articular cartilage extracted from the femoral head of a cow, we examined the viscoelasticity of the articular cartilage under a fixed load while it was immersed in distilled water, isotonic salt water, hypertonic salt water, and in hyaluronic acid. A stainless steel rod with a diameter of 1.5 mm was applied directly to the articular cartilage (weighing 25, 50 and 100 grams) and the resultant visco-elastic curves were measured. Results showed that the deformation change to the cartilage was greatest while it was immersed in hypertonic salt solution and smallest while immersed in distilled water. Secondly, when immersed in hyaluronic acid solution, the change in deformation proved to be greater when the solution was denser and the molecular weight heavier and the hyaluronic acid could not penetrate into the cartilage matrix and remained at the surface. These results demonstrated that the visco-elastic property of the articular cartilage was affected not only by the varying osmotic pressures on the internal parts of the cartilage, but also on the density of the solution surrounding the cartilage and on the different water retainability of that cartilage.

Animals↗
PubMed1996

Presence of ED-A containing fibronectin in human articular cartilage from patients with osteoarthritis and rheumatoid arthritis.

OBJECTIVE: To determine whether normal (fetal and adult) and osteoarthritic (OA) and rheumatoid arthritic (RA) cartilage express a specific isoform of fibronectin, the extra domain A (ED-A) containing fibronectin (EDA+Fn). METHODS: Presence of fibronectin (EDA+Fn and native molecule) in cartilage matrix was studied using immunohistochemical assays with specific monoclonal antibodies. Fibronectins were identified by Western blots, in synovial fluids (SF) and cartilage extracts. RESULTS: EDA+Fn was either moderately present in the surface zone or undetectable in normal cartilage, while it was increased in OA cartilage surface. In one OA cartilage sample, EDA+Fn was localized in the matrix distant from the cartilage surface (patches of staining) and its presence was confirmed by immunoblotting. In RA cartilage EDA+Fn was present in the pericellular areas of the different layers. By Western blots, the presence of EDA+Fn was confirmed in OA SF (2/3) and RA SF (3/3) (with different patterns of fragmentation). CONCLUSION: EDA+Fn generally accumulates in the surface zone of OA cartilage, where it may play a role in extracellular matrix remodelling. Its presence was more abundant in SF and in cartilage from patients with RA.

Aged↗
PubMed1996

[Magnetic resonance assessment of knee joint hyaline cartilage according to age, sex, and body weight].

To study the MR appearance of knee joint hyaline cartilage, 120 subjects were examined with MRI of the knee. Axial SE proton-density (PD) and T2, GE T1 and GE-MTC sequences were used, as well as coronal SE T1 and sagittal SE PD and T2 sequences. At the patellar and femorotibial cartilages the following variables were investigated: thickness, surface, signal intensity and visibility. Moreover, the three patellar sequences were compared qualitatively, by giving a 1-to-4 score to the images, depending on their yield in the four variables. As for articular cartilage thickness, a statistically significant difference was found between men and women in nearly all measurement sites, the mean values being always higher in men. A statistically significant inverse correlation between cartilage thickness and age was found, in men only, at the three load-bearing regions of the medial femoral condyle. Cartilage surface was irregular and/or its signal intensity altered in 28% of patients at the femoral condyles, while the cartilage of tibial plates exhibited normal surface and homogeneous signal intensity in most cases. The visibility rate of trilaminar cartilage was 82.5% for the medial femoral condyle, 87.5% for the lateral femoral condyle, 70% for the patella, 12.5% for the medial tibial plateau and 14.5% for the lateral tibial plateau. No statistically significant correlation was found between cartilage thickness, surface, signal intensity and visibility and age, sex, and body weight. The GE sequence was the best tool to study cartilage thickness and signal intensity, while the SE T2 sequence was the most accurate one to depict the articular surface and, together with the PD SE sequence, to visualize the trilaminar structure. Our study suggests that articular cartilage surface, thickness, and signal intensity can be studied accurately with SE PD and T2 sequences, combined with a GE T1 sequence.

Adolescent↗
PubMed1998

Current treatment options for the restoration of articular cartilage.

Over the past several decades, much has been learned about articular cartilage and its physiological capacity to restore itself. While articular cartilage does appear to have some regenerative capabilities, it appears to lose this capacity over a period of time, making restoration of articular surfaces more and more difficult. To date, no technique has been completely successful in achieving exactly normal regenerative articular cartilage. Arthroscopic lavage and debridement provides temporary relief of symptoms. This probably works by removing degradative enzymes that contribute to synovitis and also to the further breakdown of articular cartilage. Bone marrow stimulation techniques such as abrasion arthroplasty, drilling, and microfracture produce only fibrocartilage and therefore do not offer a long-term cure. Perichondral and periosteal interposition grafts produce repair tissue that is similar to hyaline cartilage but also lack the mechanical durability. Like bone marrow stimulation techniques, interposition grafts introduce precursor cells, which have a tendency to differentiate along lines other than cartilage. This leads to an inferior quality of repair tissue. Currently, chondrogenic-stimulating factors and artificial matrices are currently being researched and developed. Much has been learned about the various growth factors that stimulate chondrocyte differentiation and extracellular matrix production, but to date, there has not been a clinical technique that has shown any long-term promise. Ultimately, the goal will be to take precursor cells from an easily accessible source such as the iliac crest, mix them with growth factors that have been derived genetically in the lab, and provide an artificial matrix that in combination can produce restoration of articular cartilage at minimal cost and patient morbidity. Autologous osteochondral transplant systems have shown encouraging results but there are still problems. Graft matching and contouring to the recipient articular surface is difficult. Donor sites can be a limiting factor. Furthermore, the fibrocartilaginous interface between the donor and recipient site may contribute to breakdown in the long run. Autologous chondrocyte implantation is a biological repair process that also has shown encouraging results. It must be remembered that this is not normal articular cartilage--it is only hyaline-like cartilage. The technique is expensive and is technically difficult to perform. There are no randomized prospective studies that compare the natural history of the repair tissue to that of other forms of repair tissue. Long-term functional outcome is still a significant question mark. In addition, it has not been shown that autologous chondrocyte implantation can prevent degenerative changes. In the future, we probably will see delivery systems using stimulating growth factors, chondrocytes, and synthetically derived matrices. When placed in combination and with the right mechanical stimuli, we may ultimately achieve true restoration of articular cartilage.

Arthroplasty↗
PubMed1998

Changes in sulfation patterns of chondroitin sulfate in equine articular cartilage and synovial fluid in response to aging and osteoarthritis.

OBJECTIVES: To determine effects of aging on sulfation of chondroitin sulfate (CS) in articular cartilage and synovial fluid from normal equine middle carpal joints, and to determine whether CS compositional analysis can be used to assess alterations in proteoglycan turnover in degenerative cartilage obtained from horses with carpal osteochondral fractures. SAMPLE POPULATION: Carpal articular cartilage and synovial fluid from 44 cadavers with normal joints and from 16 Thoroughbred racehorses during routine carpal arthroscopic surgery. PROCEDURE: After papain/chondroitinase digestion of cartilage, CS disaccharides (unsulfated disaccharide delta Di0S, and monosulfated disaccharides delta Di4S and delta Di6S) were quantified by capillary zone electrophoresis. The CS was purified from synovial fluid chondroitinase digested, and analyzed. The CS nonreducing terminal residues, N-acetylgalctosamine (galNAc) or glucuronic acid adjacent to a 4-sulfated or 6-sulfated galNAc, were quantified. RESULTS: In cartilage, the delta Di6S-to-delta Di4S ratio increased with age; in degenerative cartilage, this ratio was not significantly different from the normal value. Percentage of delta Di0S decreased with age and was significantly higher in degenerative than in normal cartilage. The galNAc4S and galNAc4,6S represented > or = 96% of the terminal residues. There was a significant decrease in 6-sulfation of the terminal residues in degenerative cartilage. CONCLUSIONS: 6-Sulfation of internal and terminal CS residues increased with age. Cartilage degeneration in racehorses was accompanied by deposition of CS chains with altered sulfation patterns, in normal and diseased joints of horses > 2 years old, synovial fluid CS was not indicative of cartilage CS and may represent turnover products of a subpopulation of proteoglycan within the matrix.

Aging↗
PubMedDate not supplied

Behavior of tissue-engineered human cartilage after transplantation into nude mice.

Cartilage lacks the ability to regenerate structural defects. Therefore, autologous grafting has been used routinely to replace cartilaginous lesions. Because tissue engineering of human cartilage with the help of bioresorbable polymer scaffolds is possible in experimental models, the demand for the clinical application grows. In this study we present an analysis of the behavior of transplants made of human chondrocyte pools, agarose and the resorbable polymer scaffold Ethisorb and a preliminary comparison with transplants made of single patients' cells and Ethisorb but without the additional ingredient agarose. Chondrocytes were isolated from the matrix of human septal cartilage by enzymatic digestion. The pool cells were kept in monolayer culture for 2 weeks, the single patients' cells for 3-4 weeks. Chondrocyte pools were suspended in agarose and seeded into the resorbable polymer scaffold Ethisorb. Single patients' cells were seeded without agarose. All cell-polymer constructs were kept in perfusion culture for 10-14 days and transplanted subcutaneously into thymusaplastic nude mice. Additionally we implanted Ethisorb fleeces embedded in agarose without chondrocytes. After 6, 12 and 24 weeks the animals were sacrificed and the specimens were explanted and analyzed histochemically and immunohistochemically. Polymer scaffolds not seeded with chondrocytes did not show cartilage formation. Resorption was complete after 12 weeks in vivo. Transplants from cell pools remained mechanically stable over 24 weeks apart from four transplants that were resorbed completely. Cartilage formation was observed in all pool-specimens with the presence of chondronic structures and a homogeneous matrix containing hyaline cartilage-specific matrix molecules such as collagen type II. Single patients' transplants showed hyaline cartilage matrix synthesis and mechanical stability as well. Chondrocyte pools are a suitable method to study cartilage engineering of human cells in vitro and in vivo in experimental models. Under clinical conditions it is, however, necessary to study the generation of cartilage from single patients' cells. We showed that it is possible without additional ingredients such as agarose. However, variations in the preliminary results show that the clinical application with human cells is more difficult than one would expect when using human chondrocyte pools. Further studies need to be performed to find out which individual factors influence the in vitro engineered cartilage's fate in vivo.

Journal Article↗
PubMed1999

The epiphyseal cartilage and growth of long bones in Rana catesbeiana.

The structure of the epiphyseal cartilage of the bullfrog Rana catesbeiana and its role in the growth of long bones were examined. The epiphyseal cartilage was inserted into the end of a tubular bone shaft, defining three regions: articular cartilage, lateral articular cartilage and growth cartilage. Joining the lateral cartilage to the bone was a fibrous layer of periosteum, rich in blood vessels. Osteoblasts with alkaline phosphatase activity were found on the surface of the periosteal bone, which presented a fibrous non-mineralised tip. The growth cartilage was inside the bone. The proliferative chondrocytes presented perpendicular separation of daughter cells and there was no columnar arrangement of the cells. Furthermore, chondrocyte hypertrophy was not associated with either calcification or endochondral ossification, in apparent contrast to the avian and mammalian models. Finally, there was no reinforcement system capable of directing cell volume increase into longitudinal growth. Since bone extension depends on the intramembranous ossification of the periosteum, the growth cartilage is inside and not at the end of the bone and the cells in the growth cartilage show no columnar arrangement and separate in a direction perpendicular to the long bone axis, we conclude that the growth cartilage mainly contributes to the radial expansion of the bone.

Animals↗
PubMedDate not supplied

The potency of culture-expanded nasal septum chondrocytes for tissue engineering of cartilage.

Tissue engineering techniques to create extra autologous cartilage for reconstructive surgery receive more and more scientific and industrial attention. The objective of this experimental study was to assess the use of in vitro multiplied chondrocytes of the nasal septum for generation of cartilage grafts using tissue engineering techniques. Cells isolated from a biopsy of septal cartilage of rabbits and humans were expanded in culture to get a sufficient number of cells to engineer a cartilage graft. The drawback of the expansion procedure is that the cells lose their cartilaginous phenotype (dedifferentiation). We studied a method to reverse the dedifferentiation of expanded cells to stimulate them to produce cartilage matrix of good quality. Rabbit chondrocytes showed reversion of dedifferentiation (redifferentiation) when fetal calf serum was replaced by the growth factors IGF1 and TGFbeta2. This was expressed by increased glycosaminoglycan synthesis and increased numbers of collagen type II-producing cells. The redifferentiation capacity of septal cartilage cells of young rabbits was higher than that of adult rabbits. In human chondrocytes from the nasal septum redifferentiation could also be induced by replacement of serum with IGF1 and TGFbeta2. This method, however, was less efficient than in rabbits. Chondrocytes of older patients (>40 years old) were no longer sensitive to the growth factor treatment. In conclusion, our study demonstrates a method to regain cartilage phenotype in multiplied cells of nasal septum cartilage needed for tissue engineering of new cartilage. These results are promising for this technique to generate cartilage grafts for facial plastic surgery of the nasal septum.

Adult↗
PubMed2003

Cartilage-free areas in the elbow joint of young golden retrievers.

The present study describes cartilage-free areas on the ulnar trochlear notch and the humeral condyle of eight very young golden retrievers with otherwise healthy elbow joints. Remarkably, the youngest dog with full-thickness cartilage-free areas was only 8 weeks old. The younger dogs showed no macroscopic abnormalities on the locations that were affected in the older dogs. Two kinds of cartilage modifications were found. Cartilage-free areas at the edges of the articular cartilage layer were present on the humeral capitulum and on two locations of the ulna, (the medial and lateral at the base of the anconeal process, and the trochlear notch near the lateral coronoid process, which was fractured in two cases). Histological examination showed that these cartilage-free areas were filled with dense supportive tissue. Synovial cells covered this tissue as well as the surrounding hyaline cartilage. The synovial membrane covering the areas was macroscopically enlarged, but histological examination revealed no signs of inflammation. The second type of modification consisted of discoloration of the articular surface at the humeral trochlea. Histological examination revealed that in this area the articular surface was composed of fibrocartilage instead of hyaline cartilage. Apparently, there are locations within the elbow joint in which articular cartilage is not necessary for normal joint functioning. The presence of fibrocartilage on the articular surface of the humeral condyle is a surprising finding, for which no explanation has yet been found.

Age Factors↗
PubMedDate not supplied

Experimental hyaline cartilage lesions: two-dimensional spin-echo versus three-dimensional gradient-echo MR imaging.

The value of magnetic resonance (MR) imaging, with two-dimensional (2D) spin-echo and FISP (fast imaging with steady-state precession) and FLASH (fast low-angle shot) three-dimensional (3D) gradient-echo sequences, for the detection of hyaline cartilage defects of the femoral condyle and the tibial plateau, was investigated in an animal model. In eight dogs, the anterior cruciate ligament was transected in one knee joint, resulting in rapid development of osteoarthritis with degeneration of the hyaline cartilage. At autopsy, 24 cartilage lesions were found, which were classified into four grades. The overall detection of cartilage lesions with MR imaging was poor. Only five of the 24 lesions were visible on 2D spin-echo images, while 11 of 24 were visible on 3D FISP images and 15 of 24 were seen on 3D FLASH images. The best results were obtained in advanced stages of cartilage degeneration, involving ulceration and complete abrasion of the cartilage layer. Signal loss or signal intensity increase in the cartilage layer was seen inconsistently in grades 3 and 4 degeneration. In this animal model, 2D spin-echo imaging was inadequate for the diagnosis of hyaline cartilage lesions, while 3D gradient-echo imaging permitted satisfactory diagnosis in only grade 4 cartilage disease.

Animals↗
PubMed2000

Expression of cartilage oligomeric matrix protein (COMP) by embryonic and adult osteoblasts.

Cartilage oligomeric matrix protein has been implicated as an important component of endochondral ossification because of its direct effects on chondrocytes. The importance of this protein for skeletal development and growth has been recently illustrated by the identification of mutations in cartilage oligomeric protein genes in two types of inherited chondrodysplasias and osteoarthritic phenotypes: multiple epiphyseal dysplasia and pseudoachondroplasia. In the present study, we report the presence of cartilage oligomeric protein in embryonic and adult osteoblasts. A foot from a 21-week-old human fetus, subchondral bone obtained from knee replacement surgery in an adult patient, and a limb from a 19-day-postcoital mouse embryo were analyzed with immunostaining and in situ hybridization. In the human fetal foot, cartilage oligomeric protein was localized to osteoblasts of the bone collar and at the newly formed bone at the growth plate and bone diaphyses. Immunostaining was performed on the adult subchondral bone and showed positive intracellular staining for cartilage oligomeric protein of the osteoblasts lining the trabecular bone. There was no staining of the osteocytes. Immunostaining of the mouse limb showed the most intense staining for cartilage oligomeric protein in the hypertrophic chondrocytes and in the surrounding osteoblast cells of the developing bone. Cartilage oligomeric protein mRNA and protein were detected in an osteoblast cell line (MG-63), and cartilage oligomeric protein mRNA was detected from human cancellous bone RNA. These results suggest that the altered structure of cartilage oligomeric protein by the mutations seen in pseudoachondroplasia and multiple epiphyseal dysplasia may have direct effects on osteoblasts, contributing to the pathogenesis of these genetic disorders.

Animals↗
PubMed1994

Dietary lipids modify the fatty acid composition of cartilage, isolated chondrocytes and matrix vesicles.

The effects of dietary lipids on the fatty acid composition of hyaline cartilage, epiphyseal chondrocytes (EC) and matrix vesicles (MV) were evaluated in chicks. A basal semipurified diet was fed to chicks containing one of the following lipid sources at 70 g/kg: soybean oil, butter+corn oil, margarine+corn oil or menhaden oil+corn oil (MEC). Articular and epiphyseal growth cartilage were isolated from the proximal tibiotarsus; EC and MV were subsequently released by trypsin (EC 3.4.21.4) and collagenase (EC 3.4.24.3) digestion followed by ultracentrifugation. The fatty acid composition of polar lipids in chick epiphyseal cartilage at three and six weeks, as well as articular cartilage, EC and MV at eight weeks of age revealed the presence of high levels of saturated and monounsaturated fatty acids (up to 85.5%) but low levels of n-6 polyunsaturated fatty acids (PUFA) (2.6-10.2%). Mead acid (20:3n-9, > 3%) was also present in cartilage, EC and MV lipids, and was unaffected by the dietary lipid treatments. Total n-3 PUFA concentrations were the highest in cartilage, EC and MV of chicks consuming MEC. Feeding MEC lowered the levels of 20:4n-6 in cartilage, but increased 20:5n-3 levels. The data are consistent with those reported previously which showed that cartilage tissues are low in n-6 PUFA and that they contain 20:3n-9. We furthermore demonstrated that the PUFA composition of cartilage can be modified by dietary lipids.

Age Factors↗
PubMed2005

Changes in knee cartilage volume and serum COMP concentration after running exercise.

OBJECTIVE: Investigate the relationship between running induced joint loading at the knee, changes in cartilage volume and serum cartilage oligomeric matrix protein (COMP) concentration. DESIGN: Serum COMP levels and knee cartilage volumes of experienced runners were tested before and after running. Joint loading was determined using a biomechanical model of the lower extremity. BACKGROUND: To date no biomechanical rationale has been identified to explain the role of mechanical load in the aetiology of running injuries. METHODS: Blood samples and magnetic resonance imaging scans were taken before and following a 1h training run. Knee cartilage volume and serum COMP concentration were determined. Individual knee joint loading parameters were calculated from positional data and ground reaction forces. Electromyography was employed to quantify activity of main muscle groups crossing the knee joint. RESULTS: Changes in cartilage volume and COMP showed significant correlations. Net joint forces did not explain the differences in cartilage changes. Multiple regression revealed that resting COMP, COMP change after exercise and the time of co-activation of flexor and extensor muscles explain the variance of cartilage volume changes. CONCLUSIONS: Muscular co-activation was the main mechanical parameter related to cartilage changes. The current investigation elucidates the interaction of factors related to cartilage degeneration on an individual basis. Applications to altered loading conditions such as equipment or training methods offer an auspicious way of quantifying effects of interventions.

Adult↗