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Axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female Sprague Dawley rats

Chronic low back pain is a global socioeconomic crisis and treatments are lacking in part due to inadequate models. Etiological research suggests that the predominant pathology associated with chronic low back pain is intervertebral disc degeneration. Various research teams have created rat models o...

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Autores principales: Lillyman, David J., Lee, Fei San, Barnett, Evie C., Miller, Tyler J., Alvaro, Moreno Lozano, Drvol, Henry C., Wachs, Rebecca A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520768/
https://www.ncbi.nlm.nih.gov/pubmed/36203864
http://dx.doi.org/10.1002/jsp2.1212
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author Lillyman, David J.
Lee, Fei San
Barnett, Evie C.
Miller, Tyler J.
Alvaro, Moreno Lozano
Drvol, Henry C.
Wachs, Rebecca A.
author_facet Lillyman, David J.
Lee, Fei San
Barnett, Evie C.
Miller, Tyler J.
Alvaro, Moreno Lozano
Drvol, Henry C.
Wachs, Rebecca A.
author_sort Lillyman, David J.
collection PubMed
description Chronic low back pain is a global socioeconomic crisis and treatments are lacking in part due to inadequate models. Etiological research suggests that the predominant pathology associated with chronic low back pain is intervertebral disc degeneration. Various research teams have created rat models of disc degeneration, but the clinical translatability of these models has been limited by an absence of robust chronic pain‐like behavior. To address this deficit, disc degeneration was induced via an artificial annular tear in female Sprague Dawley rats. The subsequent degeneration, which was allowed to progress for 18‐weeks, caused a drastic reduction in disc volume. Furthermore, from week 10 till study conclusion, injured animals exhibited significant axial hypersensitivity. At study end, intervertebral discs were assessed for important characteristics of human degenerated discs: extracellular matrix breakdown, hypocellularity, inflammation, and nerve sprouting. All these aspects were significantly increased in injured animals compared to sham controls. Also of note, 20 significant correlations were detected between selected outcomes including a moderate and highly significant correlation (R = 0.59, p < 0.0004) between axial hypersensitivity and disc nerve sprouting. These data support this model as a rigorous platform to explore the pathobiology of disc‐associated low back pain and to screen treatments.
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spelling pubmed-95207682022-10-05 Axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female Sprague Dawley rats Lillyman, David J. Lee, Fei San Barnett, Evie C. Miller, Tyler J. Alvaro, Moreno Lozano Drvol, Henry C. Wachs, Rebecca A. JOR Spine Research Articles Chronic low back pain is a global socioeconomic crisis and treatments are lacking in part due to inadequate models. Etiological research suggests that the predominant pathology associated with chronic low back pain is intervertebral disc degeneration. Various research teams have created rat models of disc degeneration, but the clinical translatability of these models has been limited by an absence of robust chronic pain‐like behavior. To address this deficit, disc degeneration was induced via an artificial annular tear in female Sprague Dawley rats. The subsequent degeneration, which was allowed to progress for 18‐weeks, caused a drastic reduction in disc volume. Furthermore, from week 10 till study conclusion, injured animals exhibited significant axial hypersensitivity. At study end, intervertebral discs were assessed for important characteristics of human degenerated discs: extracellular matrix breakdown, hypocellularity, inflammation, and nerve sprouting. All these aspects were significantly increased in injured animals compared to sham controls. Also of note, 20 significant correlations were detected between selected outcomes including a moderate and highly significant correlation (R = 0.59, p < 0.0004) between axial hypersensitivity and disc nerve sprouting. These data support this model as a rigorous platform to explore the pathobiology of disc‐associated low back pain and to screen treatments. John Wiley & Sons, Inc. 2022-07-14 /pmc/articles/PMC9520768/ /pubmed/36203864 http://dx.doi.org/10.1002/jsp2.1212 Text en © 2022 The Authors. JOR Spine published by Wiley Periodicals LLC on behalf of Orthopaedic Research Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Lillyman, David J.
Lee, Fei San
Barnett, Evie C.
Miller, Tyler J.
Alvaro, Moreno Lozano
Drvol, Henry C.
Wachs, Rebecca A.
Axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female Sprague Dawley rats
title Axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female Sprague Dawley rats
title_full Axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female Sprague Dawley rats
title_fullStr Axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female Sprague Dawley rats
title_full_unstemmed Axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female Sprague Dawley rats
title_short Axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female Sprague Dawley rats
title_sort axial hypersensitivity is associated with aberrant nerve sprouting in a novel model of disc degeneration in female sprague dawley rats
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520768/
https://www.ncbi.nlm.nih.gov/pubmed/36203864
http://dx.doi.org/10.1002/jsp2.1212
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