Evaluation of articular changes using a rat mono-iodoacetate-induced shoulder arthritis model by histology and radiology.


Journal

Journal of orthopaedic research : official publication of the Orthopaedic Research Society
ISSN: 1554-527X
Titre abrégé: J Orthop Res
Pays: United States
ID NLM: 8404726

Informations de publication

Date de publication:
11 2023
Historique:
revised: 18 01 2023
received: 27 09 2022
accepted: 14 03 2023
medline: 23 10 2023
pubmed: 25 3 2023
entrez: 24 3 2023
Statut: ppublish

Résumé

The rat mono-iodoacetate (MIA) arthritis model has been used in studies on the hip, knee, and ankle joints. Few studies have explored its utility in shoulder arthritis research, and none have evaluated the effects of time and different MIA doses on arthritis progression. Therefore, we developed a rat MIA shoulder arthritis model to evaluate articular changes through radiological and histological analyses. Sprague-Dawley rats (n = 108) were equally divided into groups that were intra-articularly injected with 0.5 mg of MIA (in 50 µL of purified water), 2.0 mg of MIA (in 50 µL of purified water), or purified water (50 µL; sham group). Throughout the study period, 18 rats (six per group) were evaluated by computed tomography and assessed using the Larsen's classification system; 90 rats were further evaluated histologically using the Osteoarthritis Research Society International scoring system. Computed tomography revealed that the groups injected with MIA developed arthritis and osteophytes 14 days after injection, which progressed temporally. The Larsen's grades worsened over time; at all time points, the scores were higher in the group injected with 2.0 mg of MIA than in the group injected with 0.5 mg of MIA. Furthermore, concurrent with the worsening Larsen's grades, the Osteoarthritis Research Society International scores also significantly increased over time; at all time points, they were higher in the group injected with 2.0 mg of MIA than in the group injected with 0.5 mg of MIA. Our rat MIA shoulder arthritis model revealed radiologically and histologically confirmed temporal and MIA dose-dependent arthritic changes.

Identifiants

pubmed: 36959767
doi: 10.1002/jor.25560
doi:

Substances chimiques

Water 059QF0KO0R
Iodoacetic Acid WF5188V710

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2359-2366

Informations de copyright

© 2023 Orthopaedic Research Society. Published by Wiley Periodicals LLC.

Références

Teeple E, Jay GD, Elsaid KA, Fleming BC. Animal models of osteoarthritis: challenges of model selection and analysis. AAPS J. 2013;15(2):438-446.
Williams JM, Brandt KD. Iodoacetate(IA) causes osteoarthritis in guinea-pigs. Anat Rec. 1982;202:A202-A204.
Williams JM, Brandt KD. Immobilization ameliorates chemically-induced articular cartilage damage. Arthritis & Rheumatism. 1984;27(2):208-216.
Kalbhen D. Drug induces biochemical changes in cartilage metabolism: a new concept in the aetiopathogensis of osteoarthrosis. In: Nuki G, ed. The Aetiopathogensis of Osteoarthrosis. Pitman Medical Publishers; 1980:123-138.
Williams JM, Brandt KD. Temporary immobilisation facilitates repair of chemically induced articular cartilage injury. J Anat. 1984;138 (Pt 3):435-446.
Van der Kraan PM, Vitters EL, Van de Putte LB, Van den Berg WB. Development of osteoarthritic lesions in mice by “metabolic” and “mechanical” alterations in the knee joints. Am J Pathol. 1989;135(6):1001-1014.
Guingamp C, Gegout-Pottie P, Philippe L, Terlain B, Netter P, Gillet P. Mono-iodoacetate-induced experimental osteoarthritis: a dose-response study of loss of mobility, morphology, and biochemistry. Arthritis & Rheumatism. 1997;40(9):1670-1679.
Udo M, Muneta T, Tsuji K, et al. Monoiodoacetic acid induces arthritis and synovitis in rats in a dose- and time-dependent manner: proposed model-specific scoring systems. Osteoarthritis Cartilage. 2016;24(7):1284-1291.
Philpott HT, O'Brien M, McDougall JJ. Attenuation of early phase inflammation by cannabidiol prevents pain and nerve damage in rat osteoarthritis. Pain. 2017;158(12):2442-2451.
Williams JM, Brandt KD. Triamcinolone hexacetonide protects against fibrillation and osteophyte formation following chemically induced articular cartilage damage. Arthritis & Rheumatism. 1985;28(11):1267-1274.
Marker CL, Pomonis JD. The monosodium iodoacetate model of osteoarthritis. Pain Res. 2012;851:239-248.
Ichiseki T, Shimasaki M, Ueda Y, et al. Intraarticularly-injected mesenchymal stem cells stimulate anti-inflammatory molecules and inhibit pain related protein and chondrolytic enzymes in a monoiodoacetate-induced rat arthritis model. Int J Mol Sci. 2018;19(1):203.
Vargas CA, Baptista CAC, del Sol M, et al. Development of an ultrathin sheet plastination technique in rat humeral joints with osteoarthritis induced by monosodium iodoacetate for neovascularization study. Anat Sci Int. 2020;95(2):297-303.
Ochiai N, Ohtori S, Kenmoku T, et al. Sensory innervation of rat contracture shoulder model. J Shoulder Elbow Surg. 2013;22(2):158-164.
Hashimoto E, Ochiai N, Kenmoku T, et al. Macroscopic and histologic evaluation of a rat model of chronic rotator cuff tear. J Shoulder Elbow Surg. 2016;25(12):2025-2033.
Liu X, Manzano G, Kim HT, Feeley BT. A rat model of massive rotator cuff tears. J Orthop Res. 2011;29(4):588-595.
Kramer EJ, Bodendorfer BM, Laron D, et al. Evaluation of cartilage degeneration in a rat model of rotator cuff tear arthropathy. J Shoulder Elbow Surg. 2013;22(12):1702-1709.
Charan J, Kantharia ND. How to calculate sample size in animal studies? J Pharmacol Pharmacother. 2013;4(4):303-306.
Larsen A, Dale K, Eek M. Radiographic evaluation of rheumatoid arthritis and related conditions by standard reference films. Acta Radiol, Diagn. 1977;18(4):481-491.
Solymossy C, Dixey J, Utley M, et al. Larsen scoring of digitized X-ray images. Rheumatology. 1999;38(11):1127-1129.
Pritzker KPH, Gay S, Jimenez SA, et al. Osteoarthritis cartilage histopathology: grading and staging. Osteoarthritis Cartilage. 2006;14(1):13-29.
Yamanashi Y, Ohmichi M, Ohmichi Y, et al. Efficacy of methotrexate on rat knee osteoarthritis induced by monosodium iodoacetate. J Inflamm Res. 2021;14:3247-3259.
Mohan G, Perilli E, Kuliwaba JS, Humphries JM, Parkinson IH, Fazzalari NL. Application of in vivo micro-computed tomography in the temporal characterisation of subchondral bone architecture in a rat model of low-dose monosodium iodoacetate-induced osteoarthritis. Arthritis Res Ther. 2011;13(6):R210.
Guzman RE, Evans MG, Bove S, Morenko B, Kilgore K. Mono-Iodoacetate-Induced histologic changes in subchondral bone and articular cartilage of rat femorotibial joints: AN animal model of osteoarthritis. Toxicol Pathol. 2003;31(6):619-624.
Pomonis JD, Boulet JM, Gottshall SL, et al. Development and pharmacological characterization of a rat model of osteoarthritis pain. Pain. 2005;114(3):339-346.
Kawarai Y, Orita S, Nakamura J, et al. Analgesic effect of duloxetine on an animal model of monosodium Iodoacetate-Induced hip osteoarthritis. J Orthop Res. 2020;38(2):422-430.
Miyahara N, Kokubo T, Hara Y, Yamada A, Koike T, Arai Y. Evaluation of X-ray doses and their corresponding biological effects on experimental animals in cone-beam micro-CT scans (R-mCT2). Radiol Phys Technol. 2016;9(1):60-68.
Mustafy T, Benoit A, Londono I, Moldovan F, Villemure I. Can repeated in vivo micro-CT irradiation during adolescence alter bone microstructure, histomorphometry and longitudinal growth in a rodent model? PLoS One. 2018;13(11):e0207323.
Nwosu LN, Mapp PI, Chapman V, Walsh DA. Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA). Osteoarthritis Cartilage. 2016;24(11):1910-1917.
Yoh S, Kawarai Y, Hagiwara S, et al. Intra-articular injection of monoiodoacetate induces diverse hip osteoarthritis in rats, depending on its dose. BMC Musculoskelet Disord. 2022;23(1):494.
Kuyinu EL, Narayanan G, Nair LS, Laurencin CT. Animal models of osteoarthritis: classification, update, and measurement of outcomes. J Orthop Surg Res. 2016;11(1):19.
Williams JM, Brandt KD. Exercise increases osteophyte formation and diminishes fibrillation following chemically induced articular cartilage injury. J Anat. 1984;139 (Pt 4):599-611.
Williams JM, Brandt KD. Benoxaprofen reduces osteophyte formation and fibrillation after articular cartilage injury. J Rheumatol. 1985;12(1):27-32.
Hoshino T, Tsuji K, Onuma H, et al. Persistent synovial inflammation plays important roles in persistent pain development in the rat knee before cartilage degradation reaches the subchondral bone. BMC Musculoskelet Disord. 2018;19(1):291.
Smolen JS, Aletaha D, McInnes IB. Rheumatoid arthritis. The Lancet. 2016;388(10055):2023-2038.
Dreier R, Ising T, Ramroth M, Rellmann Y. Estradiol inhibits ER Stress-Induced apoptosis in chondrocytes and contributes to a reduced osteoarthritic cartilage degeneration in female mice. Front Cell Dev Biol. 2022;10(May):1-11.

Auteurs

Shohei Ise (S)

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba City, Japan.

Nobuyasu Ochiai (N)

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba City, Japan.

Eiko Hashimoto (E)

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba City, Japan.

Naoya Hirosawa (N)

Department of Orthopaedic Surgery, Nagareyama Central Hospital, Nagareyama, Japan.

Daisuke Kajiwara (D)

Department of Orthopaedic Surgery, Seirei Sakura Citizen Hospital, Sakura, Japan.

Yohei Shimada (Y)

Department of Orthopaedic Surgery, St. Marianna University School of Medicine, Kawasaki, Japan.

Kenta Inagaki (K)

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba City, Japan.

Yu Hiraoka (Y)

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba City, Japan.

Fumiya Hattori (F)

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba City, Japan.

Seiji Ohtori (S)

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba City, Japan.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH