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Changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee

We assessed the pathological changes of articular cartilage and subchondral bone on different locations of the knee after extracorporeal shockwave therapy (ESWT) in early osteoarthritis (OA). Rat knees under OA model by anterior cruciate ligament transaction (ACLT) and medial meniscectomy (MM) to in...

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Autores principales: Wang, Ching-Jen, Cheng, Jai-Hong, Chou, Wen-Yi, Hsu, Shan-Ling, Chen, Jen-Hung, Huang, Chien-Yiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370283/
https://www.ncbi.nlm.nih.gov/pubmed/28367081
http://dx.doi.org/10.7150/ijms.17469
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author Wang, Ching-Jen
Cheng, Jai-Hong
Chou, Wen-Yi
Hsu, Shan-Ling
Chen, Jen-Hung
Huang, Chien-Yiu
author_facet Wang, Ching-Jen
Cheng, Jai-Hong
Chou, Wen-Yi
Hsu, Shan-Ling
Chen, Jen-Hung
Huang, Chien-Yiu
author_sort Wang, Ching-Jen
collection PubMed
description We assessed the pathological changes of articular cartilage and subchondral bone on different locations of the knee after extracorporeal shockwave therapy (ESWT) in early osteoarthritis (OA). Rat knees under OA model by anterior cruciate ligament transaction (ACLT) and medial meniscectomy (MM) to induce OA changes. Among ESWT groups, ESWT were applied to medial (M) femur (F) and tibia (T) condyles was better than medial tibia condyle, medial femur condyle as well as medial and lateral (L) tibia condyles in gross osteoarthritic areas (p<0.05), osteophyte formation and subchondral sclerotic bone (p<0.05). Using sectional cartilage area, modified Mankin scoring system as well as thickness of calcified and un-calcified cartilage analysis, the results showed that articular cartilage damage was ameliorated and T+F(M) group had the most protection as compared with other locations (p<0.05). Detectable cartilage surface damage and proteoglycan loss were measured and T+F(M) group showed the smallest lesion score among other groups (p<0.05). Micro-CT revealed significantly improved in subchondral bone repair in all ESWT groups compared to OA group (p<0.05). There were no significantly differences in bone remodeling after ESWT groups except F(M) group. In the immunohistochemical analysis, T+F(M) group significant reduced TUNEL activity, promoted cartilage proliferation by observation of PCNA marker and reduced vascular invasion through observation of CD31 marker for angiogenesis compared to OA group (P<0.001). Overall the data suggested that the order of the effective site of ESWT was T+F(M) ≧ T(M) > T(M+L) > F(M) in OA rat knees.
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spelling pubmed-53702832017-03-31 Changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee Wang, Ching-Jen Cheng, Jai-Hong Chou, Wen-Yi Hsu, Shan-Ling Chen, Jen-Hung Huang, Chien-Yiu Int J Med Sci Research Paper We assessed the pathological changes of articular cartilage and subchondral bone on different locations of the knee after extracorporeal shockwave therapy (ESWT) in early osteoarthritis (OA). Rat knees under OA model by anterior cruciate ligament transaction (ACLT) and medial meniscectomy (MM) to induce OA changes. Among ESWT groups, ESWT were applied to medial (M) femur (F) and tibia (T) condyles was better than medial tibia condyle, medial femur condyle as well as medial and lateral (L) tibia condyles in gross osteoarthritic areas (p<0.05), osteophyte formation and subchondral sclerotic bone (p<0.05). Using sectional cartilage area, modified Mankin scoring system as well as thickness of calcified and un-calcified cartilage analysis, the results showed that articular cartilage damage was ameliorated and T+F(M) group had the most protection as compared with other locations (p<0.05). Detectable cartilage surface damage and proteoglycan loss were measured and T+F(M) group showed the smallest lesion score among other groups (p<0.05). Micro-CT revealed significantly improved in subchondral bone repair in all ESWT groups compared to OA group (p<0.05). There were no significantly differences in bone remodeling after ESWT groups except F(M) group. In the immunohistochemical analysis, T+F(M) group significant reduced TUNEL activity, promoted cartilage proliferation by observation of PCNA marker and reduced vascular invasion through observation of CD31 marker for angiogenesis compared to OA group (P<0.001). Overall the data suggested that the order of the effective site of ESWT was T+F(M) ≧ T(M) > T(M+L) > F(M) in OA rat knees. Ivyspring International Publisher 2017-02-23 /pmc/articles/PMC5370283/ /pubmed/28367081 http://dx.doi.org/10.7150/ijms.17469 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wang, Ching-Jen
Cheng, Jai-Hong
Chou, Wen-Yi
Hsu, Shan-Ling
Chen, Jen-Hung
Huang, Chien-Yiu
Changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee
title Changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee
title_full Changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee
title_fullStr Changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee
title_full_unstemmed Changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee
title_short Changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee
title_sort changes of articular cartilage and subchondral bone after extracorporeal shockwave therapy in osteoarthritis of the knee
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370283/
https://www.ncbi.nlm.nih.gov/pubmed/28367081
http://dx.doi.org/10.7150/ijms.17469
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