Intra-articular injections of high-molecular-weight hyaluronic acid have biphasic effects on joint inflammation and destruction in rat antigen-induced arthritis
© Roth et al, licensee BioMed Central Ltd. 2005
Received: 6 December 2004
Accepted: 1 March 2005
Published: 31 March 2005
To assess the potential use of hyaluronic acid (HA) as adjuvant therapy in rheumatoid arthritis, the anti-inflammatory and chondroprotective effects of HA were analysed in experimental rat antigen-induced arthritis (AIA). Lewis rats with AIA were subjected to short-term (days 1 and 8, n = 10) or long-term (days 1, 8, 15 and 22, n = 10) intra-articular treatment with microbially manufactured, high-molecular-weight HA (molecular weight, 1.7 × 106 Da; 0.5 mg/dose). In both tests, 10 buffer-treated AIA rats served as arthritic controls and six healthy animals served as normal controls. Arthritis was monitored by weekly assessment of joint swelling and histological evaluation in the short-term test (day 8) and in the long-term test (day 29). Safranin O staining was employed to detect proteoglycan loss from the epiphyseal growth plate and the articular cartilage of the arthritic knee joint. Serum levels of IL-6, tumour necrosis factor alpha and glycosaminoglycans were measured by ELISA/kit systems (days 8 and 29). HA treatment did not significantly influence AIA in the short-term test (days 1 and 8) but did suppress early chronic AIA (day 15, P < 0.05); however, HA treatment tended to aggravate chronic AIA in the long-term test (day 29). HA completely prevented proteoglycan loss from the epiphyseal growth plate and articular cartilage on day 8, but induced proteoglycan loss from the epiphyseal growth plate on day 29. Similarly, HA inhibited the histological signs of acute inflammation and cartilage damage in the short-term test, but augmented acute and chronic inflammation as well as cartilage damage in the long-term test. Serum levels of IL-6, tumour necrosis factor alpha, and glycosaminoglycans were not influenced by HA. Local therapeutic effects of HA in AIA are clearly biphasic, with inhibition of inflammation and cartilage damage in the early chronic phase but with promotion of joint swelling, inflammation and cartilage damage in the late chronic phase.
Rheumatoid arthritis (RA), a chronic systemic disease primarily affecting the joints, is characterised by progressive destruction of cartilage and bony structures of the joints [1, 2]. Its social impact results from the personal suffering of patients as well as from medical and indirect costs .
Hyaluronic acid (HA) is a large linear glycosaminoglycan composed of repeating disaccharide units of glucuronic acid and N-acetylglucosamine, linked via the 1–4 position of the sugar rings . The synovial fluid in the joint consists of ultrafiltrated plasma and HA, the latter being produced by type-B synoviocytes of the lining layer . Inflammatory changes lead to depolymerisation of HA, resulting in a decrease of its molecular weight and its concentration . Its lubricant properties decrease, contributing to the destruction of cartilage and bone .
HA protects cells and anatomical structures against mechanical overloading due to its viscoelastic characteristics . The viscosity of the synovial fluid is reduced in patients with RA , a deficit that can be balanced by the supply of exogenous HA . In addition, the production of endogenous synovial HA is stimulated via the supply of exogenous HA .
RA is characterised by a loss of proteoglycans in the affected joints [12, 13]. HA possesses chondroprotective effects [10, 14] and is reported to inhibit the loss of proteoglycans from the matrix of joint cartilage [15, 16]. HA also blocks the loss of proteoglycans caused by the addition of catalytic cytokines to cultivated cartilage [17, 18] and suppresses the degradation of cartilage matrix mediated by fibronectin fragments [19, 20]. HA is also reported to protect the cartilage against proteoglycan loss, against chondrocyte cell death caused by free oxygen radicals, IL-1, or mononuclear-cell-enriched medium, and against other alterations [14, 15, 21–24]. Cartilage degradation induced by neutrophil leukocytes is also reduced by HA in vitro . Injection of exogenous HA induces a decrease of inflammatory and proliferative processes within the synovium . Also, HA inhibits the proliferation  and migration of white blood cells , and affects their adherence, chemotaxis, and phagocytosis properties [11, 29, 30]. Degradation of HA by reactive oxygen species, on the other hand, may reduce the protective properties of HA [14, 31].
In spite of the known potential benefits of HA on a number of pathological features of RA, a general estimate of its validity for the treatment of RA is still lacking, particularly in terms of experimental studies in animal models of arthritis. The present study was therefore designed to examine the effects of HA in rat antigen-induced arthritis (AIA). This experimental monoarticular arthritis shares some characteristics of RA; for example, hyperplasia of the synovial membrane, inflammatory infiltration of the joints, and destruction of cartilage . This model is also useful to characterise treatment responses; for example, the reduction of inflammation or changes in the synovial connective tissue .
Materials and methods
Female Lewis rats (10–12 weeks of age) were obtained from the Institute of Animal Studies, Friedrich Schiller University Jena, Germany. The rats were housed under standard conditions, in a 12-hour light/dark cycle. The animals were fed with standard rodent chow and water ad libitum. The rats were divided into two groups: non-arthritic animals (n = 6) and arthritic animals (n = 40). The latter were subdivided into the following groups (each n = 10): untreated AIA rats, short-term test (US); untreated AIA rats, long-term test (UL); HA-treated AIA rats, short-term test (HS); and HA-treated AIA rats, long-term test (HL). All animal studies were approved by the governmental committee for animal protection.
Pyrogen-free, sterile-filtered HA with a molecular weight of 1.7 × 106 Da was used, obtained by biotechnological fermentation from Streptococcus equisimilis ssp. zooepidemicus V 2541. This bacterial HA, also called non-animal-source hyaluronan, is completely identical to human HA. The content of pyrogen was minimised to less than 0.05 IE/ml HA by cleaning steps, therefore fulfilling the demands of the European Pharmacopeia (Supplement 2001, page 1472). The zero-viscosity of the purified 1.0% high-molecular-weight HA (molecular weight, 1.7 × 106 Da) in 0.9% NaCl solution amounted to h0 = 10.74 Pa s. The injection units contained 10 mg HA in 1 ml of 0.9% NaCl.
Induction of AIA
All experimental animals were immunised by two subcutaneous injections (days -21 and -14) of 0.5 g methylated bovine serum albumin (mBSA), dissolved in 0.5 ml saline and emulsified with 0.5 ml complete Freund's adjuvant [32, 34]. Knee monoarticular arthritis was induced 2 weeks after the second immunisation via a single joint injection of 0.5 mg mBSA (50 μl of 10 mg/ml mBSA dissolved in 0.9% NaCl) into the right knee joint (day 0 of AIA). The left knee remained without injection.
Treatment with HA
On day 1 of AIA, all 40 arthritic animals received an intra-articular injection into the right inflamed knee joint. HA-treated AIA rats (groups HS and HL) received in each case 0.5 mg HA (50 μl of 10 mg/ml HA in 0.9% NaCl), whereas the untreated AIA rats (groups US and UL) received 50 μl PBS. The AIA rats of the long-term test received further injections at the beginning of each subsequent week (days 8, 15, and 22): the HL group received 50 μl HA, and the UL group received 50 μl PBS.
The short-term test (groups US and HS) was terminated 1 week after the first injection of HA or PBS (day 8). The long-term test (groups UL and HL) was terminated 1 week after the fourth injection (day 29).
In all cases, the contralateral (left) knee joint remained untreated. The group of six non-arthritic animals without AIA (12 weeks of age) served for the collection of normal values.
All injections (including those necessary to induce immunisation and knee AIA) were performed under ether anaesthesia. At the end of the experiment, the animals were sacrificed using an overdose of CO2 and cervical dislocation.
Collection of samples
Blood samples were collected by heart puncture after opening the thorax. The blood was centrifuged for 10 min at 3000 × g and ambient temperature. The serum was divided into three portions of at least 250 μl and was frozen at -80°C until analysis.
The knee joints were disconnected from the long bones and stored in 6% formaldehyde. In order to ensure an optimal impregnation with formaldehyde, the adhering remainders of the long bones were kept very short (approximately 1.0 cm above and below the joint space) and the dorsal joint capsule was opened.
Evaluation of arthritis
Joint swelling, body weight, and the general state of the animals were regularly monitored. The measurements of weight and mediolateral joint diameter took place on days 0, 1, 4, 8, 15, 22, and 29. The mediolateral joint diameter was measured using a vernier caliper [32, 34].
All preparations were stored in 6% formaldehyde for 24 hours. Decalcification in ethylenediamine tetraacetic acid subsequently took place and the preparations were embedded in paraffin. After the removal of paraffin, 5-μm thick sections were cut .
For the assessment of the histological arthritis scores, the sections were stained with haematoxylin and eosin. All slides were evaluated by an independent observer who was blinded to the design and details of the study. In all cases, three sections per knee joint were examined and scored using a semiquantitative scale.
The extent of acute joint inflammation – as defined by the degree of infiltration of the synovial membrane by polymorphonuclear leukocytes, and defined by the exudation of granulocytes in the joint space – was evaluated in each case with 0 = no changes, 1 = mild changes, 2 = moderate changes, and 3 = severe changes. In addition, the presence (score 1) or absence (score 0) of fibrin exudation in the joint space and periarticular inflammation was assessed, resulting in a maximum total score of 8 for acute inflammation.
Chronic joint inflammation – based on the parameters hyperplasia of synovial lining cells, infiltration by mononuclear cells, and fibrosis of synovial membrane or periarticular tissue – was evaluated with a score of 0–3, resulting in a maximum total score of 9.
The extent of the damage to articular cartilage and adjacent bone structures (cell necrosis, structural bone, and cartilage defects) was evaluated with score 0 = no damage, score 1 = <5% of the cartilage surface affected, score 2 = 5–10% of the cartilage surface affected, score 3 = 10–50% of the cartilage surface affected, and score 4 = >50% of the cartilage surface affected (maximal total score of 4).
Safranin O staining was performed to estimate the proteoglycan content in the cartilage [36–38]. In order to obtain comparable histological results, all slides were stained using exactly the same procedure . The preparations were analysed under defined conditions using a Zeiss microscope Axiovert 200 M (20 × magnification) (Carl Zeiss, Göttingen, Germany)] and the results were stored as pixel pictures. The staining intensity was determined in 175 × 25 mm2 areas, using Scion Image software (Scion Corporation, Frederick, MD, USA).
Cytokine and serum glycosaminoglycan evaluation
The serum levels of IL-6, tumour necrosis factor alpha (TNF-α) and glycosaminoglycan (GAG) were determined at the end point of the short-term test (day 8) and at the endpoint of the long-term test (day 29).
The serum levels of IL-6 and TNF-α were determined using a commercial sandwich ELISA kits for rats according to the manufacturer's instructions (Biosource International, Camalliro, CA, USA). The detection limits were 8 pg/ml for IL-6 and 4 pg/ml for TNF-α. According to the manufacturer, there was no cross-reactivity with other rat cytokines.
The serum levels of total GAG were measured in non-diluted serum with a commercially available kit. The standard values for healthy rats were 10.8–17.4 mg/l (Glycane T Labor + Diagnostica, Freital, Germany).
Statistical evaluations were carried out using the programme SigmaStat 2.0. Since nearly all data were not normally distributed, the non-parametric Mann–Whitney U test was used. Data were expressed as means and standard errors of the means. P ≤ 0.05 was considered statistically significant for α.
In cases in which P values for α were at the limits of significance (0.05 ≤ P ≤ 0.1; joint swelling day 29, cartilage damage day 8), the statistical power of the U test was determined using the actual difference at a given time point as delta.
Because for the time period from day 0 to day 8 the procedure and results did not differ between the US and UL groups or between the HS and HL groups, respectively, the values from the short-term test and the long-term test were pooled for statistical evaluation of this period in both cases.
At baseline, the body weight was 188 ± 29 g (untreated AIA rats) and 197 ± 22 g (HA-treated AIA rats). After a plateau between day 0 and day 8 in both untreated rats and HA-treated AIA rats, the body weight rose in concomitance with the decrease of arthritis severity. At the end of the long-term test (day 29), the animals weighed 213 ± 15 g (untreated AIA rats) and 230 ± 13 g (HA-treated AIA rats). The differences between the groups did not reach statistical significance at any time point.
Intra-articular treatment with HA did not significantly affect the degree of joint swelling on days 1, 4, and 8 (Fig. 2). On day 15 (groups UL and HL, n = 10 each) there was a significant reduction of joint swelling in the HA-treated AIA group compared with the untreated AIA group (P < 0.05). On day 22 the swelling was no longer significantly different from the untreated AIA group (P = 0.37); in fact, it was even somewhat higher. On day 29 (end of the long-term test) the small increase of joint swelling in the HA-treated AIA group persisted (as compared with the untreated AIA group), although without reaching statistical significance (power 1 β = 0.851).
In general, therefore, HA seemed to positively affect the early chronic phase of AIA (day 15), but did not have an influence on the acute or late chronic phases of AIA, at least in terms of joint swelling.
Loss of proteoglycans from the epiphyseal growth plate of the femoral condyle and the articular cartilage
In the long-term test (day 29) there was no significant loss of proteoglycan content in the epiphyseal growth plate of untreated AIA rats (see Fig. 3). However, treatment with HA was characterised by a significant proteoglycan loss in the growth plate of the arthritic right knee compared with the contralateral knee or with the right knee joint of non-arthritic animals (P < 0.001; Fig. 3).
In the different layers of the articular cartilage, the untreated AIA rats no longer showed any significant proteoglycan loss; that is, there were no significant differences between the right knee joints and left knee joints of AIA rats, or between the right knee joint of AIA rats and the right knee joint of non-arthritic animals (Fig. 5; Safranin O staining data not shown). Treatment with HA did not significantly affect the proteoglycan content in any layer of the articular cartilage.
Histological scores of arthritis and cartilage damage
In the short-term test (day 8) a clear score for chronic inflammation was also observed (Figs 4a,c,e and 6b), without significant differences between untreated and HA-treated AIA groups. The chronic inflammation significantly decreased from day 8 to day 29 in untreated and HA-treated AIA (group US versus group UL, P < 0.001; group HS versus group HL, P < 0.01; Figs 4c,e,g,h and 6b). Unexpectedly, however, on day 29 the chronic inflammation score was more pronounced in the animals treated with HA compared with the untreated AIA group (P < 0.05; Figs 4g,h and 6b).
In terms of cartilage damage, the untreated AIA group was characterised by a maximum individual score of 3; that is, the maximal possible score of 4 was not observed (Fig. 6c). On day 8, the mean cartilage damage was somewhat more pronounced in the untreated AIA group, but without significant differences in comparison with the HA-treated AIA group (power 1 - β = 0.821). From day 8 to day 29, the cartilage damage decreased significantly in untreated rats and HA-treated AIA rats (group US versus group UL, P < 0.001; group HS versus group HL, P < 0.01). In the long-term test (day 29), however, the cartilage damage was significantly higher in the animals treated with HA than in the untreated AIA group (P < 0.05; Fig. 6c).
Systemic cytokine levels
As for TNF-α, non-arthritic animals had mean serum levels of 5.45 ± 4.56 pg/ml (Fig. 7b). In the short-term test these values were increased both in the untreated and in the HA-treated AIA groups, but not to a significant degree. In the long-term test, the mean TNF-α levels were very similar to those of non-arthritic animals. Treatment with HA did not significantly influence TNF-α levels at either time point (Fig. 7b).
Serum GAG levels
In non-arthritic animals, the mean serum levels of GAG were 12.70 ± 3.30 μg/ml (Fig. 7c). Untreated AIA rats had significantly higher GAG levels than non-arthritic animals in the short-term test and in the long-term test (P < 0.05 and P < 0.001, respectively; significance not indicated in Fig. 7). Treatment with HA had no influence on this parameter at either time point (Fig. 7c).
Clinical parameters of arthritis
Treatment with HA did not reduce joint swelling in the acute phase, as significant reduction of joint swelling was found only on day 15 (i.e. in the early chronic phase of AIA). The temporary reduction of joint swelling may be a result of the reduced acute inflammation observed histologically at an earlier time point (day 8). This anti-inflammatory effect of HA is consistent with the effects previously reported in collagen-induced arthritis [22, 40] and human RA [41, 42].
Interestingly, however, while the joint swelling continued to progressively and spontaneously decrease in untreated AIA, it persisted in HA-treated animals after day 15, although the difference remained at the limits of significance (P = 0.06). The persistence of inflammation after prolonged application of HA (day 29) is further substantiated by significant proteoglycan loss in the epiphyseal growth plate, by significant persistence of both acute and chronic inflammation, and by significantly increased histological signs of articular cartilage damage. This biphasic course regarding joint inflammation and destruction after repeated application of high-molecular-weight HA has not been previously described. HA therefore probably shows only a limited temporal window of anti-inflammatory activity in arthritis.
Adverse reactions to HA have been described in human osteoarthritis, either after the first injection and subsequent intra-articular injections or at the beginning of a new treatment course. These adverse events consisted of pain and/or transient swelling of the injected joint, mostly mild or moderate in intensity [43–45]. The adverse reactions observed upon intra-articular treatment of human osteoarthritis are not comparable with the biphasic effects in the present study, since they were only short-lasting and limited to a period immediately following injection.
Proteoglycans in the epiphyseal growth plate of the femoral condyle and the articular cartilage
AIA was accompanied by a significant loss of proteoglycans in the epiphyseal growth plate of untreated AIA rats in the short-term test (significantly ameliorated by HA; day 8). This proteoglycan loss is probably caused by the inflammatory micromilieu in the arthritic joint  and the adjacent periarticular bone marrow , in analogy to the alterations of the primary and secondary spongiosa in AIA . The significant prevention of proteoglycan loss from the epiphyseal growth plate by HA at this time point may be due to the clear anti-arthritic effects of HA, as also documented by the significant decrease of acute inflammation on day 8 (Fig. 6a). Whether intra-articular treatment with HA indirectly influences the inflammatory changes in the bone marrow, thereby preventing proteoglycan loss in the epiphyseal growth plate, remains to be investigated.
Unexpectedly, repeated intra-articular HA treatment induced proteoglycan loss in the epiphyseal growth plate in the long-term test (day 29). This late loss of proteoglycans in the epiphysis under prolonged HA treatment suggests late proinflammatory effects of HA, as also indicated by significantly elevated levels of acute and chronic inflammation, as well as cartilage damage (Fig. 6).
Regarding the proteoglycan content within the articular cartilage, HA completely prevented the proteoglycan loss in the short-term test. This applied to the severe loss of proteoglycans in the superficial layer — the layer most strongly affected in the present study (37%) and also that most strongly affected in the fibronectin-mediated arthritis model . This prevention also applied to deeper layers of the calcified cartilage, however, indicating either deep-reaching effects of intra-articular HA (up to 100 μm; see Fig. 1) or an indirect effect on the micromilieu in the epiphyseal bone core. Such profound chondroprotective effects of HA have not previously been reported in an in vivo arthritis model. Previous in vitro studies, in which the proteoglycan release from the cell matrix of bovine chondrocyte cultures was inhibited by HA, have suggested a covering of the matrix of as a mechanism for the chondroprotective capacity of HA .
Acute and chronic inflammation, and cartilage damage
HA reduced the histological signs of acute inflammation in the short-term test (day 8). At this point, HA also showed a tendency (P = 0.06) to protect the joint again against cartilage damage (Fig. 6c). The tendency for decreased cartilage damage in the short-term test supports the assumption that HA forms a temporary protecting barrier over the cartilage, and thereby protects it against degradation [16, 19, 49]. The known reduction of free oxygen radicals , as well as the reduction of cytokines and other mediators of acute inflammation by HA [15, 21], could contribute to both its chondroprotective capacity (Fig. 6c) and its anti-inflammatory effects (Fig. 6a) in early chronic AIA (day 8).
In the long-term test (day 29) HA treatment was associated with significantly higher histological signs of acute and chronic inflammation and, more importantly, with more severe cartilage damage. The late proinflammatory effects of repeated HA application, in parallel to the late loss of epiphysis proteoglycans and late damage of articular cartilage (see earlier), point to an interdependence of inflammation and damage in HA-treated AIA rats at this stage.
Significantly higher histological signs of articular cartilage damage after repeated HA application (day 29) are in contrast to a non-altered proteoglycan content of the articular cartilage at this time (Fig. 5). A seemingly normal proteoglycan content may therefore not be sufficient to exclude structural damage of the articular cartilage in arthritis. Consequently, more sensitive in vivo procedures will have to be established to reliably assess functional or structural cartilage alterations before irreversible damage occurs .
Serum levels of cytokines and GAG
In the present study, the systemic levels of IL-6, TNF-α and GAG were not significantly influenced by intra-articular administration of high-molecular-weight HA, indicating that both anti-inflammatory effects (day 8) and proinflammatory effects (day 29) are locally restricted.
In conclusion, HA appears to have a limited therapeutic window for local treatment of arthritis, as shown by amelioration of clinical signs (day 15), by prevention of proteoglycan loss in the articular cartilage and epiphyseal growth plate, and by prevention of structural cartilage damage, as well as by the reduction of acute inflammation in the arthritic joint (day 8).
Late aggravation of clinical signs (not significant, day 29), proteoglycan loss from the epiphyseal growth plate, and acute/chronic inflammation and structural cartilage damage at this time point strongly indicate biphasic effects of local HA treatment.
Whether these biphasic effects are due to accumulation of HA beyond pathological levels (which may be avoidable by single injection instead of repeated injection) or whether certain phases of the clinical course render the animals sensitive to the proinflammatory effects of HA remains the subject of future research, both in animal models and in human RA.
= antigen-induced arthritis
= enzyme-linked immunosorbent assay
= hyaluronic acid
- HL = HA-treated AIA rats:
- HS = HA-treated AIA rats:
= methylated bovine serum albumin
= phosphate-buffered saline
= rheumatoid arthritis
= tumour necrosis factor alpha
- UL = untreated AIA rats:
- US = untreated AIA rats:
The authors are grateful to Dr Frank Brand, Mrs K Neumann, and Mrs K Axt (Department of Clinical Chemistry and Laboratory Diagnostics, Rudolf-Elle Hospital) for determination of laboratory values, and to Cordula Müller and Jana Schömburg (Research Department, Rudolf-Elle Hospital) for preparation of the histological sections. They are also grateful to Dr A Notni, Dr K Bergmann, and Dr R Winter (Department of Orthopaedics, Rudolf-Elle Hospital), as well as to Dr C Wicher and Mrs P Dobermann (Institute of Animal Studies, Friedrich-Schiller University Jena) for assistance in the animal experiments.
- Firestein GS, Zvaifler NJ: Rheumatoid arthritis: a disease of disordered immunity. Inflammation: Basic Principles and Clincal Correlates. Edited by: Gallin J, Goldstein I, Willis K. 1992, New York: Raven Press, 959-975.Google Scholar
- Gay S, Gay RE, Koopman WJ: Molecular and cellular mechanisms of joint destruction in rheumatois arthritis: two cellular mechanisms explain joint destruction?. Ann Rheum Dis. 1993, 52 (Suppl 1): 39-47.View ArticleGoogle Scholar
- Mau W, Bornmann M, Weber H, Weidemann HF, Hecker H, Raspe HH: Prediction of permanent work disability in a follow-up study of early rheumatoid arthritis: results of a tree structured analysis using RECPAM. Br J Rheumatol. 1996, 35: 652-659.View ArticlePubMedGoogle Scholar
- Balazs EA, Iozzo RV: Matrix proteoglycans: from molecular design to cellular function. Annu Rev Biochem. 1998, 67: 609-652. 10.1146/annurev.biochem.67.1.609.View ArticleGoogle Scholar
- Laurent TC, Laurent UB, Fraser JR: The structure and function of hyaluronan: an overview. Immunol Cell Biol. 1996, 74: 1-7.View ArticleGoogle Scholar
- Miossec P, Dinarello CA, Ziff M: Interleukin-1 lymphocyte chemotactic activity in rheumatoid arthritis synovial fluid. Arthritis Rheum. 1986, 29: 461-470.View ArticlePubMedGoogle Scholar
- Dahl LB, Dahl IM, Engström-Laurent A, Granath K: Concentration and molecular weight of sodium hyaluronate in synovial fluid from patients with rheumatoid arthritis and other arthropathies. Ann Rheum Dis. 1985, 44: 817-822.PubMed CentralView ArticlePubMedGoogle Scholar
- Balazs EA, Denlinger JL: Sodium hyaluronate and joint function. J Equine Vet Sci. 1985, 5: 217-228.View ArticleGoogle Scholar
- Duffy JM, McNally GM, O'Gorman A, Spedding PL, Grimshaw J, Grimshaw JT, Walker B, Guthrie DJS, Mollan RAB: Viscometic studies of pathological human synovial fluids. J Orthop Rheumatol. 1994, 7: 99-106.Google Scholar
- Namiki O, Toyoshima H, Morisaki N: Therapeutic effect of intra-articular injection of high molecular weight hyaluronic acid on osteoarthritis of the knee. Int J Clin Pharmacol Ther Toxicol. 1982, 20: 501-507.PubMedGoogle Scholar
- Watterson JR, Esdaile JM: Viscosupplementation: therapeutic mechanisms and clinical potential in osteoarthritis of the knee. J Am Acad Orthop Surg. 2000, 8: 277-284.PubMedGoogle Scholar
- Saxne T, Wollheim FA, Pettersson H, Heinegard D: Proteoglycan concentration in synovial fluid: predictor of future cartilage destruction in rheumatoid arthritis?. Br Med J (Clin Res Ed). 1987, 295: 1447-1448.View ArticleGoogle Scholar
- Bensouyad A, Hollander AP, Dularay B, Bedwell AE, Cooper RA, Hutton CW, Dieppe PA, Elson CJ: Concentrations of glycosaminoglycans in synovial fluids and their relation with immunological and inflammatory mediators in rheumatoid arthritis. Ann Rheum Dis. 1990, 49: 301-307.PubMed CentralView ArticlePubMedGoogle Scholar
- Sato H, Takahashi T, Ide H, Fukushima T, Tabata M, Sekine F, Kobayashi K, Negishi M, Niwa Y: Antioxidant activity of synovial fluid, hyaluronic acid, and two subcomponents of hyaluronic acid. Synovial fluid scavenging effect is enhanced in rheumatoid arthritis patients. Arthritis Rheum. 1988, 31: 63-71.View ArticlePubMedGoogle Scholar
- Larsen NE, Lombard KM, Parent EG, Balazs EA: Effect of hylan on cartilage and chondrocyte cultures. J Orthop Res. 1992, 10: 23-32. 10.1002/jor.1100100104.View ArticlePubMedGoogle Scholar
- Shimazu A, Jikko A, Iwamoto M, Koike T, Yan W, Okada Y, Shinmei M, Nakamura S, Kato Y: Effects of hyaluronic acid on the release of proteoglycan from the cell matrix in rabbit chondrocyte cultures in the presence and absence of cytokines. Arthritis Rheum. 1993, 36: 247-253.View ArticlePubMedGoogle Scholar
- Morris ES, Wilcon S, Treadwell BV: Inhibition of interleukin 1-mediated proteoglycan degradation in bovine articular cartilage explants by addition of sodium hyaluronate. Am J Vet Res. 1992, 53: 1977-1982.PubMedGoogle Scholar
- Akatsuka M, Yamamoto Y, Tobetto K, Yasui T, Ando T: In vitro effects of hyaluronan on prostaglandin E2 induction by interleukin-1 in rabbit articular chondrocytes. Agents Actions. 1993, 38: 122-125.View ArticlePubMedGoogle Scholar
- Homandberg GA, Hui F, Wen C, Kuettner KE, Williams JM: Hyaluronic acid suppresses fibronectin fragment mediated cartilage chondrolysis: I. In vitro. Osteoarthritis Cartilage. 1997, 5: 309-319.View ArticlePubMedGoogle Scholar
- Williams JM, Plaza V, Hui F, Wen C, Kuettner KE, Homandberg GA: Hyaluronic acid suppresses fibronectin fragment mediated cartilage chondrolysis: II. In vivo. Osteoarthritis Cartilage. 1997, 5: 235-240.View ArticlePubMedGoogle Scholar
- Presti D, Scott JE: Hyaluronan-mediated protective effect against cell damage caused by enzymatically produced hydroxyl (OH.) radicals is dependent on hyaluronan molecular mass. Cell Biochem Funct. 1994, 12: 281-288.View ArticlePubMedGoogle Scholar
- Campo GM, Avenoso A, Campo S, Ferlazzo AM, Altavilla D, Calatroni : Efficacy of treatment with glycosaminoglycans on experimental collagen-induced arthritis in rats. Arthritis Res Ther. 2003, 5: R122-R131. 10.1186/ar748.PubMed CentralView ArticlePubMedGoogle Scholar
- Abatangelo G, Cortivo R, Govoni E, De Galateo A, Brun P: Hyaluronate reverses inhibition of proteoglycan synthesis by oxygen free radicals in cultured chick embryonic cartilage [abstract]. Eur J Cell Biol. 1989, 49 (Suppl 28): 18-Google Scholar
- Cortivo R, Brun P, Cardarelli L, O'Regan M, Radice M, Abatangelo G: Antioxidant effects of hyaluronan and its alpha-methyl-prednisolone derivative in chondrocyte and cartilage cultures. Semin Arthritis Rheum. 1996, 26: 492-501. 10.1016/S0049-0172(96)80030-8.View ArticlePubMedGoogle Scholar
- Tobetto K, Nakai K, Akatsuka M, Yasui T, Ando T, Hirano S: Inhibitory effects of hyaluronan on neutrophil-mediated cartilage degradation. Connect Tissue Res. 1993, 29: 181-190.View ArticlePubMedGoogle Scholar
- Goldberg RL, Toole BP: Hyaluronate inhibition of cell proliferation. Arthritis Rheum. 1987, 30: 769-778.View ArticlePubMedGoogle Scholar
- Anastassiades T, Robertson W: Modulation of mitogen-dependent lymphocyte stimulation by hyaluronic acid. J Rheumatol. 1984, 11: 729-734.PubMedGoogle Scholar
- Corrado EM, Peluso GF, Gigliotti S, Durante C, Palmieri D, et al: The effects of intraarticular administration of hyaluronan on osteoarthritis of the knee: a clinical study with immunological and biochemical evaluations. Eur J Rheum Inflamm. 1993, 15: 547-576.Google Scholar
- Forrester JV, Balazs EA: Inhibition of phagocytosis by high molecular weight hyaluronate. Immunology. 1980, 40: 435-446.PubMed CentralPubMedGoogle Scholar
- Håkansson L, Hällgren R, Venge P: Regulation of granulocyte function by hyaluronic acid. In vitro and in vivo effects on phagocytosis, locomotion, and metabolism. J Clin Invest. 1980, 66: 298-305.PubMed CentralView ArticlePubMedGoogle Scholar
- Greenwald RA: Oxygen radicals, inflammation, and arthritis: pathophysiological considerations and implications for treatment. Semin Arthritis Rheum. 1991, 20: 219-240. 10.1016/0049-0172(91)90018-U.View ArticlePubMedGoogle Scholar
- Bräuer R, Kittlick PD, Thoss K, Henzgen S: Different immunological mechanisms contribute to cartilage destruction in antigen-induced arthritis. Exp Toxicol Pathol. 1994, 46: 383-388.View ArticlePubMedGoogle Scholar
- Griffiths RJ: The use of animals in the search for anti-inflammatory drugs. Mechanisms and Models in Rheumatoid Arthritis. Edited by: Henderson B, Edwards JCW, Pettpher ER. 1995, London: Academic PressGoogle Scholar
- Buchner E, Bräuer R, Schmidt C, Emmrich F, Kinne RW: Induction of flare-up reactions in rat antigen-induced arthritis. J Autoimmun. 1995, 8: 61-74.PubMedGoogle Scholar
- Romeis B: Mikroskopische Technik. Mikroskopische Technik. Edited by: Böck P. 1989, Urban-Schwarzenberg, München, 17Google Scholar
- Rosenberg L: Chemical basis for the histological use of safranin O in the study of articular cartilage. J Bone Joint Surg Am. 1971, 53: 69-82.PubMedGoogle Scholar
- Kiviranta I, Jurvelin J, Tammi M, Saamanen AM, Helminen HJ: Microspectrophotometric quantitation of glycosaminoglycans in articular cartilage sections stained with Safranin O. Histochemistry. 1985, 82: 249-255. 10.1007/BF00501401.View ArticlePubMedGoogle Scholar
- Arokoski J, Kiviranta I, Jurvelin J, Tammi M, Helminen HJ: Long-distance running causes site-dependent decrease of cartilage glycosaminoglycan content in the knee joints of beagle dogs. Arthritis Rheum. 1993, 36: 1451-1459.View ArticlePubMedGoogle Scholar
- Meyer P, Burkhardt H, Palombo-Kinne E, Grunder W, Bräuer R, Stiller KJ, Kalden JR, Becker W, Kinne RW: 123I-antileukoproteinase scintigraphy reveals microscopic cartilage alterations in the contralateral knee joint of rats with 'monarticular' antigen-induced arthritis. Arthritis Rheum. 2000, 43: 298-310. 10.1002/1529-0131(200002)43:2<298::AID-ANR9>3.0.CO;2-G.View ArticlePubMedGoogle Scholar
- Campo GM, Avenoso A, Campo S, Ferlazzo A, Altavilla D, Micali C, Calatroni A: Aromatic trap analysis of free radicals production in experimental collagen-induced arthritis in the rat: protective effect of glycosaminoglycans treatment. Free Radic Res. 2003, 37: 257-268. 10.1080/1071576021000046640.View ArticlePubMedGoogle Scholar
- Tanaka N, Sakahashi H, Sato E, Hirose K, Ishima T, Ishii S: Intra-articular injection of high molecular weight hyaluronan after arthrocentesis as treatment for rheumatoid knees with joint effusion. Rheumatol Int. 2002, 22: 151-154. 10.1007/s00296-002-0214-y.View ArticlePubMedGoogle Scholar
- Goto M, Hanyu T, Yoshio T, Matsuno H, Shimizu M, Murata N, Shiozawa S, Matsubara T, Yamana S, Matsuda T: Intra-articular injection of hyaluronate (SI-6601D) improves joint pain and synovial fluid prostaglandin E2 levels in rheumatoid arthritis: a multicenter clinical trial. Clin Exp Rheumatol. 2001, 19: 377-383.PubMedGoogle Scholar
- Puttick MP, Wade JP, Chalmers A, Connell DG, Rangno KK: Acute local reactions after intraarticular hylan for osteoarthritis of the knee. J Rheumatol. 1995, 22: 1311-1314.PubMedGoogle Scholar
- Allen E, Krohn K: Adverse reaction to Hylan GF-20 [Letter]. J Rheumatol. 2000, 27: 1572-PubMedGoogle Scholar
- Martens PB: Bilateral symmetric inflammatory reaction to hylan G-F 20 injection. Arthritis Rheum. 2001, 44: 978-979. 10.1002/1529-0131(200104)44:4<978::AID-ANR156>3.0.CO;2-N.View ArticlePubMedGoogle Scholar
- Simon J, Surber R, Kleinstauber G, Petrow PK, Henzgen S, Kinne RW, Brauer R: Systemic macrophage activation in locally-induced experimental arthritis. J Autoimmun. 2001, 17: 127-136. 10.1006/jaut.2001.0534.View ArticlePubMedGoogle Scholar
- Kinne RW, Brauer R, Stuhlmuller B, Palombo-Kinne E, Burmester GR: Macrophages in rheumatoid arthritis. Arthritis Res. 2000, 2: 189-202. 10.1186/ar86.PubMed CentralView ArticlePubMedGoogle Scholar
- Oelzner P, Bräuer R, Henzgen S, Thoss K, Wunsche B, Hersmann G, Abendroth K, Kinne RW: Periarticular bone alterations in chronic antigen-induced arthritis: free and liposome-encapsulated clodronate prevent loss of bone mass in the secondary spongiosa. Clin Immunol. 1999, 90: 79-88. 10.1006/clim.1998.4623.View ArticlePubMedGoogle Scholar
- Bräuer R, Kette H, Henzgen S, Thoss K: Influence of cyclosporin A on cytokine levels in synovial fluid and serum of rats with antigen-induced arthritis. Agents Actions. 1994, 41: 96-98.View ArticlePubMedGoogle Scholar
- Gray ML, Eckstein F, Peterfy C, Dahlberg L, Kim YJ, Sorensen AG, Smith RL: Toward imaging biomarkers for osteoarthritis. Clin Orthop. 2004, 427 (Suppl): 175-181.View ArticleGoogle Scholar
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