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Chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone

BACKGROUND: To investigate the effect of intra-articular injection of Chitosan (Cs) added to hyaluronic acid (HA) on subchondral bone during osteoarthritis (OA), microarchitectural parameters and mineral density were measured in a rabbit model of early OA. A novel hybrid hydrogel adding reacetylated...

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Autores principales: Rieger, R., Boulocher, C., Kaderli, S., Hoc, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557071/
https://www.ncbi.nlm.nih.gov/pubmed/28810851
http://dx.doi.org/10.1186/s12891-017-1700-4
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author Rieger, R.
Boulocher, C.
Kaderli, S.
Hoc, T.
author_facet Rieger, R.
Boulocher, C.
Kaderli, S.
Hoc, T.
author_sort Rieger, R.
collection PubMed
description BACKGROUND: To investigate the effect of intra-articular injection of Chitosan (Cs) added to hyaluronic acid (HA) on subchondral bone during osteoarthritis (OA), microarchitectural parameters and mineral density were measured in a rabbit model of early OA. A novel hybrid hydrogel adding reacetylated Cs of fungal origin to HA was compared to high molecular weight HA commercial formulation. METHOD: Eighteen rabbits underwent unilateral anterior cruciate ligament transection (ACLT) and were divided into three groups (Saline-group, HA-group and Hybrid-group) depending on the intra-articular injection compound. Eight contralateral knees were used as non-operated controls (Contralateral-group). Micro-computed tomography was performed six weeks post-ACLT to study subchondral bone microarchitectural parameters and mineral density at an early stage of OA development. RESULTS: Cartilage thickness mean value was reduced only in Saline-group compared to Contralateral-group. When the Hybrid-group was compared to Saline-group, subchondral bone microarchitectural parameters (trabecular thickness and trabecular bone volume fraction) were significantly changed; subchondral bone plate and trabecular bone mineral densities (bone mineral density and tissue mineral density) were reduced. When the Hybrid-group was compared to HA-group, subchondral bone microarchitectural parameters (subchondral plate thickness and trabecular thickness) and trabecular bone mineral densities (bone mineral density and tissue mineral density) were significantly decreased. CONCLUSION: Conclusion: Compared to HA alone, the novel hybrid hydrogel, constituted of Cs added to HA, enhanced microarchitectural parameters and mineral density changes, leading to subchondral bone loss in a rabbit model of early experimental OA.
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spelling pubmed-55570712017-08-16 Chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone Rieger, R. Boulocher, C. Kaderli, S. Hoc, T. BMC Musculoskelet Disord Research Article BACKGROUND: To investigate the effect of intra-articular injection of Chitosan (Cs) added to hyaluronic acid (HA) on subchondral bone during osteoarthritis (OA), microarchitectural parameters and mineral density were measured in a rabbit model of early OA. A novel hybrid hydrogel adding reacetylated Cs of fungal origin to HA was compared to high molecular weight HA commercial formulation. METHOD: Eighteen rabbits underwent unilateral anterior cruciate ligament transection (ACLT) and were divided into three groups (Saline-group, HA-group and Hybrid-group) depending on the intra-articular injection compound. Eight contralateral knees were used as non-operated controls (Contralateral-group). Micro-computed tomography was performed six weeks post-ACLT to study subchondral bone microarchitectural parameters and mineral density at an early stage of OA development. RESULTS: Cartilage thickness mean value was reduced only in Saline-group compared to Contralateral-group. When the Hybrid-group was compared to Saline-group, subchondral bone microarchitectural parameters (trabecular thickness and trabecular bone volume fraction) were significantly changed; subchondral bone plate and trabecular bone mineral densities (bone mineral density and tissue mineral density) were reduced. When the Hybrid-group was compared to HA-group, subchondral bone microarchitectural parameters (subchondral plate thickness and trabecular thickness) and trabecular bone mineral densities (bone mineral density and tissue mineral density) were significantly decreased. CONCLUSION: Conclusion: Compared to HA alone, the novel hybrid hydrogel, constituted of Cs added to HA, enhanced microarchitectural parameters and mineral density changes, leading to subchondral bone loss in a rabbit model of early experimental OA. BioMed Central 2017-08-15 /pmc/articles/PMC5557071/ /pubmed/28810851 http://dx.doi.org/10.1186/s12891-017-1700-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Rieger, R.
Boulocher, C.
Kaderli, S.
Hoc, T.
Chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone
title Chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone
title_full Chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone
title_fullStr Chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone
title_full_unstemmed Chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone
title_short Chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone
title_sort chitosan in viscosupplementation: in vivo effect on rabbit subchondral bone
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557071/
https://www.ncbi.nlm.nih.gov/pubmed/28810851
http://dx.doi.org/10.1186/s12891-017-1700-4
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