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The Effect of a Cyclooxygenase 2 Inhibitor on Early Degenerated Human Nucleus Pulposus Explants
Study Design Preclinical in vitro culture of human degenerated nucleus pulposus (NP) tissue. Objective Cyclooxygenase 2 inhibitors (e.g., celecoxib) inhibit prostaglandin E(2) (PGE(2)) production, and they have been shown to upregulate regeneration of articular cartilage. In this study, we developed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908972/ https://www.ncbi.nlm.nih.gov/pubmed/24494179 http://dx.doi.org/10.1055/s-0033-1359724 |
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author | van Dijk, Bart Potier, Esther Licht, Ruud Creemers, Laura Ito, Keita |
author_facet | van Dijk, Bart Potier, Esther Licht, Ruud Creemers, Laura Ito, Keita |
author_sort | van Dijk, Bart |
collection | PubMed |
description | Study Design Preclinical in vitro culture of human degenerated nucleus pulposus (NP) tissue. Objective Cyclooxygenase 2 inhibitors (e.g., celecoxib) inhibit prostaglandin E(2) (PGE(2)) production, and they have been shown to upregulate regeneration of articular cartilage. In this study, we developed an explant culture system for use with human tissue and tested the potential of celecoxib. Methods NP explants were cultured with or without 1 μM of celecoxib and were analyzed at days 0 and 7 for biochemical content (water, sulfated glycosaminoglycans, hydroxyproline, and DNA), gene expression (for disk matrix anabolic and catabolic markers), and PGE(2) content. Results Water and biochemical contents as well as gene expression remained close to native values after 1 week of culture. PGE(2) levels were not increased in freshly harvested human NP tissue and thus were not reduced in treated tissues. Although no anabolic effects were observed at the dosage and culture duration used, no detrimental effects were observed and some specimens did respond by lowering PGE(2). Conclusions Human degenerated NP explants were successfully cultured in a close to in vivo environment for 1 week. Further research, especially dosage-response studies, is needed to understand the role of PGE(2) in low back pain and the potential of celecoxib to treat painful disks. |
format | Online Article Text |
id | pubmed-3908972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-39089722015-02-01 The Effect of a Cyclooxygenase 2 Inhibitor on Early Degenerated Human Nucleus Pulposus Explants van Dijk, Bart Potier, Esther Licht, Ruud Creemers, Laura Ito, Keita Global Spine J Article Study Design Preclinical in vitro culture of human degenerated nucleus pulposus (NP) tissue. Objective Cyclooxygenase 2 inhibitors (e.g., celecoxib) inhibit prostaglandin E(2) (PGE(2)) production, and they have been shown to upregulate regeneration of articular cartilage. In this study, we developed an explant culture system for use with human tissue and tested the potential of celecoxib. Methods NP explants were cultured with or without 1 μM of celecoxib and were analyzed at days 0 and 7 for biochemical content (water, sulfated glycosaminoglycans, hydroxyproline, and DNA), gene expression (for disk matrix anabolic and catabolic markers), and PGE(2) content. Results Water and biochemical contents as well as gene expression remained close to native values after 1 week of culture. PGE(2) levels were not increased in freshly harvested human NP tissue and thus were not reduced in treated tissues. Although no anabolic effects were observed at the dosage and culture duration used, no detrimental effects were observed and some specimens did respond by lowering PGE(2). Conclusions Human degenerated NP explants were successfully cultured in a close to in vivo environment for 1 week. Further research, especially dosage-response studies, is needed to understand the role of PGE(2) in low back pain and the potential of celecoxib to treat painful disks. Georg Thieme Verlag KG 2013-10-23 2014-02 /pmc/articles/PMC3908972/ /pubmed/24494179 http://dx.doi.org/10.1055/s-0033-1359724 Text en © Thieme Medical Publishers |
spellingShingle | Article van Dijk, Bart Potier, Esther Licht, Ruud Creemers, Laura Ito, Keita The Effect of a Cyclooxygenase 2 Inhibitor on Early Degenerated Human Nucleus Pulposus Explants |
title | The Effect of a Cyclooxygenase 2 Inhibitor on Early Degenerated Human Nucleus Pulposus Explants |
title_full | The Effect of a Cyclooxygenase 2 Inhibitor on Early Degenerated Human Nucleus Pulposus Explants |
title_fullStr | The Effect of a Cyclooxygenase 2 Inhibitor on Early Degenerated Human Nucleus Pulposus Explants |
title_full_unstemmed | The Effect of a Cyclooxygenase 2 Inhibitor on Early Degenerated Human Nucleus Pulposus Explants |
title_short | The Effect of a Cyclooxygenase 2 Inhibitor on Early Degenerated Human Nucleus Pulposus Explants |
title_sort | effect of a cyclooxygenase 2 inhibitor on early degenerated human nucleus pulposus explants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908972/ https://www.ncbi.nlm.nih.gov/pubmed/24494179 http://dx.doi.org/10.1055/s-0033-1359724 |
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