Experimental osteoarthritis model by means of medial meniscectomy in rats and effects of diacerein administration and hyaluronic acid injection

Authors

  • Marcia Uchôa Rezende Faculdade de Medicina, Universidade de São Paulo (FMUSP)
  • Arnaldo José Hernandez Faculdade de Medicina, Universidade de São Paulo (FMUSP)
  • Claudia Regina Gomes Cardim Mendes Oliveira Faculdade de Medicina, Universidade de São Paulo (FMUSP)
  • Raul Bolliger Neto Faculdade de Medicina, Universidade de São Paulo (FMUSP)

Keywords:

Osteoarthritis., Knee., Anthraquinones, Hyaluronic acid, Models, animal.

Abstract

CONTEXT AND OBJECTIVE: The development of a slow and progressive mechanical model for osteoarthritis is important for correlation with clinical practice, and for evaluating the effects of disease-modifying medications. A mechanical osteoarthritis model was developed to evaluate the effects of intra-articular hyaluronic acid (HA) injection and oral diacerein administration. DESIGN AND SETTING: Experimental study at the Department of Orthopedics and Traumatology, Uni-versidade de São Paulo. METHOD: Total medial meniscectomy was performed on seven groups of ten Wistar rats each, com- prising four control groups (C) and three study groups (S). C.I: operated, non-medicated; C.II: operated, injections of HA vehicle; C.III: non-operated, non-medicated; C.IV: operated, non-medicated, sacrificed three months post-meniscectomy; S.I: operated, receiving intra-articular HA injections; S.II: operated, oral diacerein from the third to the seventh postoperative month; S.III: operated, received both medications. All the animals (except C.IV) were sacrificed seven months post-meniscectomy. All femurs and tibias were assessed histologically. RESULTS: The most severe degenerative histological changes were in the tibias of the operated knees. On the contralateral side, all groups had mild changes on the tibial surface. The femoral surface had slight changes. C.I showed severe changes. S.II results matched those of C.IV. HA protected the tibial surface. S.II and S.III had similar results. CONCLUSIONS: 1) The experimental model produced mild arthritis after three months and severe arthritis after seven months; 2) diacerein reduced the degenerative changes in both knees; 3) HA protected the joint cartilage; 4) Combining the two drugs did not improve the results.

Downloads

Download data is not yet available.

Author Biographies

Marcia Uchôa Rezende, Faculdade de Medicina, Universidade de São Paulo (FMUSP)

MD, PhD. Collaborating Professor, Department of Orthopedics and Traumatology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.

Arnaldo José Hernandez, Faculdade de Medicina, Universidade de São Paulo (FMUSP)

MD, PhD. Associate Professor, Department of Orthopedics and Traumatology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.

Claudia Regina Gomes Cardim Mendes Oliveira, Faculdade de Medicina, Universidade de São Paulo (FMUSP)

MD, PhD. Collaborating Professor, Department of Orthopedics and Traumatology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.

Raul Bolliger Neto, Faculdade de Medicina, Universidade de São Paulo (FMUSP)

MD, PhD. Collaborating Professor, Department of Orthopedics and Traumatology, Faculdade de Medicina, Universidade de São Paulo (FMUSP), São Paulo, Brazil.

References

Altman R, Asch E, Bloch D, et al. Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association. Arthritis Rheum. 1986;29(8):1039-49.

Colombo C, Butler M, O’Byrne E, et al. A new model of osteoarthritis in rabbits. I. Development of knee joint pathology following lateral meniscectomy and section of the fibular collateral and sesamoid ligaments. Arthritis Rheum. 1983;26(7):875-86.

Zhang W, Nuki G, Moskowitz RW, et al. OARSI recommendations for the management of hip and knee osteoarthritis: part III: Changes in evidence following systematic cumulative update of research published through January 2009. Osteoarthritis Cartilage. 2010;18(4):476-99.

Setnikar I. Antireactive properties of “chondroprotective” drugs. Int J Tissue React. 1992;14(5):253-61.

Ghosh P, Read R, Numata Y, et al. The effects of intraarticular administration of hyaluronan in a model of early osteoarthritis in sheep. II. Cartilage composition and proteoglycan metabolism. Semin Arthritis Rheum. 1993;22(6 Suppl 1):31-42.

Savarino L, Fioravanti A, Leo G, Aloisi R, Mian M. Anthraquinone-2,6-disulfonic acid as a disease-modifying osteoarthritis drug: an in vitro and in vivo study. Clin Orthop Relat Res. 2007;461:231-7.

Silberberg M, Silberberg R. Osteoarthrosis in mice fed diets enriched with animal or vegetable fat. Arch Pathol. 1960;70:385-90.

Moskowitz RW, Davis W, Sammarco J, et al. Experimentally induced degenerative joint lesions following partial meniscectomy in the rabbit. Arthritis Rheum. 1973;16(3):397-405.

Marshall JL. Periarticular osteophytes. Initiation and formation in the knee of the dog. Clin Orthop Relat Res. 1969;62:37-47.

Pond MJ, Nuki G. Experimentally-induced osteoarthritis in the dog. Ann Rheum Dis. 1973;32(4):387-8.

Cake M, Read R, Edwards S, et al. Changes in gait after bilateral meniscectomy in sheep: effect of two hyaluronan preparations. J Orthop Sci. 2008;13(6):514-23.

Cox JS, Nye CE, Schaefer WW, Woodstein IJ. The degenerative effects of partial and total resection of the medial meniscus in dogs’ knees. Clin Orthop Relat Res. 1975;(109):178-83.

Shapiro F, Glimcher MJ. Induction of osteoarthrosis in the rabbit knee joint. Clin Orthop Relat Res. 1980;(147):287-95.

Colombo C, Butler M, Hickman L, et al. A new model of osteoarthritis in rabbits. II. Evaluation of anti-osteoarthritic effects of selected antirheumatic drugs administered systemically. Arthritis Rheum. 1983;26(9):1132-9.

Butler M, Colombo C, Hickman L, et al. A new model of osteoarthritis in rabbits. III. Evaluation of anti-osteoarthritic effects of selected drugs administered intraarticularly. Arthritis Rheum. 1983;26(11):1380-6.

Mazières B, Berdah L, Thiéchart M, Viguier G. [Diacetylrhein on a postcontusion model of experimental osteoarthritis in the rabbit]. Rev Rhum Ed Fr. 1993;60(6 Pt 2):77S-81S.

Sakakibara Y, Miura T, Iwata H, et al. Effect of high-molecular-weight sodium hyaluronate on immobilized rabbit knee. Clin Orthop Relat Res. 1994;(299):282-92.

Smith GN Jr, Myers SL, Brandt KD, Mickler EA. Effect of intraarticular hyaluronan injection in experimental canine osteoarthritis. Arthritis Rheum. 1998;41(6):976-85.

Rosner IA, Goldberg VM, Getzy L, Moskowitz RW. Effects of estrogen on cartilage and experimentally induced osteoarthritis. Arthritis Rheum. 1979;22(1):52-8.

Decaris E, Guingamp C, Chat M, et al. Evidence for neurogenic transmission inducing degenerative cartilage damage distant from local inflammation. Arthritis Rheum. 1999;42(9):1951-60.

Brandt KD, Smith GN Jr, Simon LS. Intraarticular injection of hyaluronan as treatment for knee osteoarthritis: what is the evidence? Arthritis Rheum. 2000;43(6):1192-203.

Schiavinato A, Lini E, Guidolin D, et al. Intraarticular sodium hyaluronate injections in the Pond-Nuki experimental model of osteoarthritis in dogs. II. Morphological findings. Clin Orthop Relat Res. 1989;(241):286-99.

Gomis A, Miralles A, Schmidt RF, Belmonte C. Intra-articular injections of hyaluronan solutions of different elastoviscosity reduce nociceptive nerve activity in a model of osteoarthritic knee joint of the guinea pig. Osteoarthritis Cartilage. 2009;17(6):798-804.

Amiel D, Frey C, Woo SL, Harwood F, Akeson W. Value of hyaluronic acid in the prevention of contracture formation. Clin Orthop Relat Res. 1985;(196):306-11.

Hsieh YS, Yang SF, Lue KH, Chu SC, Lu KH. Effects of different molecular weight hyaluronan products on the expression of urokinase plasminogen activator and inhibitor and gelatinases during the early stage of osteoarthritis. J Orthop Res. 2008;26(4):475-84.

Listrat V, Ayral X, Patarnello F, et al. Arthroscopic evaluation of potential structure modifying activity of hyaluronan (Hyalgan) in osteoarthritis of the knee. Osteoarthritis Cartilage. 1997;5(3):153-60.

Guidolin DD, Ronchetti IP, Lini E, Guerra D, Frizziero L. Morphological analysis of articular cartilage biopsies from a randomized, clinical study comparing the effects of 500-730 kDa sodium hyaluronate (Hyalgan) and methylprednisolone acetate on primary osteoarthritis of the knee. Osteoarthritis Cartilage. 2001;9(4):371-81.

Yoshimi T, Kikuchi T, Obara T, et al. Effects of high-molecular-weight sodium hyaluronate on experimental osteoarthosis induced by the resection of rabbit anterior cruciate ligament. Clin Orthop Relat Res. 1994;(298):296-304.

Williams JM, Plaza V, Hui F, et al. Hyaluronic acid suppresses fibronectin fragment mediated cartilage chondrolysis: II. In vivo. Osteoarthritis Cartilage. 1997;5(4):235-40.

Rezende MU, Gurgel HM, Vilaça Junior PR, et al. Diacerhein versus glucosamine in a rat model of osteoarthritis. Clinics (Sao Paulo). 2006;61(5):461-6.

Legendre F, Bogdanowicz P, Martin G, et al. Rhein, a diacerhein-derived metabolite, modulates the expression of matrix degrading enzymes and the cell proliferation of articular chondrocytes by inhibiting ERK and JNK-AP-1 dependent pathways. Clin Exp Rheumatol. 2007;25(4):546-55.

Malaguti C, Vilella CA, Vieira KP, et al. Diacerhein downregulate proinflammatory cytokines expression and decrease the autoimmune diabetes frequency in nonobese diabetic (NOD) mice. Int Immunopharmacol. 2008;8(6):782-91.

Downloads

Published

2015-01-01

How to Cite

1.
Rezende MU, Hernandez AJ, Oliveira CRGCM, Bolliger Neto R. Experimental osteoarthritis model by means of medial meniscectomy in rats and effects of diacerein administration and hyaluronic acid injection. Sao Paulo Med J [Internet]. 2015 Jan. 1 [cited 2025 Mar. 9];133(1):4-12. Available from: https://periodicosapm.emnuvens.com.br/spmj/article/view/1022

Issue

Section

Original Article