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Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA)

OBJECTIVES: To address the hypothesis that different types of established osteoarthritis (OA) pain behaviours have associations with different aspects of articular pathology, we investigated the relationship between structural knee joint pathology and pain behaviour following injection of a low vs a...

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Autores principales: Nwosu, L.N., Mapp, P.I., Chapman, V., Walsh, D.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: W.B. Saunders For The Osteoarthritis Research Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081684/
https://www.ncbi.nlm.nih.gov/pubmed/27349460
http://dx.doi.org/10.1016/j.joca.2016.06.012
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author Nwosu, L.N.
Mapp, P.I.
Chapman, V.
Walsh, D.A.
author_facet Nwosu, L.N.
Mapp, P.I.
Chapman, V.
Walsh, D.A.
author_sort Nwosu, L.N.
collection PubMed
description OBJECTIVES: To address the hypothesis that different types of established osteoarthritis (OA) pain behaviours have associations with different aspects of articular pathology, we investigated the relationship between structural knee joint pathology and pain behaviour following injection of a low vs a high dose of monosodium iodoacetate (MIA) in the rat. METHODS: Rats received a single intra-articular injection of 0.1 mg or 1 mg MIA or saline (control). Pain behaviour (hind limb weight bearing asymmetry (WB) and hindpaw withdrawal threshold (PWT) to punctate stimulation) was assessed. Cartilage and synovium were examined by macroscopic visualisation of articular surfaces and histopathology. RESULTS: Both doses of MIA lowered PWTs, 1 mg MIA also resulted in WB asymmetry. Both doses were associated with cartilage macroscopic appearance, proteoglycan loss, abnormal chondrocyte morphology, increased numbers of vessels crossing the osteochondral junction, synovitis and macrophage infiltration into the synovium. PWTs were more strongly associated with chondrocyte morphology, synovitis and macrophage infiltration than with loss of cartilage surface integrity. CONCLUSIONS: Both pain behaviours were associated with OA structural severity and synovitis. Differences in pain phenotype following low vs higher dose of MIA were identified despite similar structural pathology. OA structural pathology as traditionally measured only partially explains the MIA-induced pain phenotype.
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spelling pubmed-50816842016-11-01 Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA) Nwosu, L.N. Mapp, P.I. Chapman, V. Walsh, D.A. Osteoarthritis Cartilage Article OBJECTIVES: To address the hypothesis that different types of established osteoarthritis (OA) pain behaviours have associations with different aspects of articular pathology, we investigated the relationship between structural knee joint pathology and pain behaviour following injection of a low vs a high dose of monosodium iodoacetate (MIA) in the rat. METHODS: Rats received a single intra-articular injection of 0.1 mg or 1 mg MIA or saline (control). Pain behaviour (hind limb weight bearing asymmetry (WB) and hindpaw withdrawal threshold (PWT) to punctate stimulation) was assessed. Cartilage and synovium were examined by macroscopic visualisation of articular surfaces and histopathology. RESULTS: Both doses of MIA lowered PWTs, 1 mg MIA also resulted in WB asymmetry. Both doses were associated with cartilage macroscopic appearance, proteoglycan loss, abnormal chondrocyte morphology, increased numbers of vessels crossing the osteochondral junction, synovitis and macrophage infiltration into the synovium. PWTs were more strongly associated with chondrocyte morphology, synovitis and macrophage infiltration than with loss of cartilage surface integrity. CONCLUSIONS: Both pain behaviours were associated with OA structural severity and synovitis. Differences in pain phenotype following low vs higher dose of MIA were identified despite similar structural pathology. OA structural pathology as traditionally measured only partially explains the MIA-induced pain phenotype. W.B. Saunders For The Osteoarthritis Research Society 2016-11 /pmc/articles/PMC5081684/ /pubmed/27349460 http://dx.doi.org/10.1016/j.joca.2016.06.012 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nwosu, L.N.
Mapp, P.I.
Chapman, V.
Walsh, D.A.
Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA)
title Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA)
title_full Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA)
title_fullStr Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA)
title_full_unstemmed Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA)
title_short Relationship between structural pathology and pain behaviour in a model of osteoarthritis (OA)
title_sort relationship between structural pathology and pain behaviour in a model of osteoarthritis (oa)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5081684/
https://www.ncbi.nlm.nih.gov/pubmed/27349460
http://dx.doi.org/10.1016/j.joca.2016.06.012
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