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Inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model

BACKGROUND: The vertebral endplate route was demonstrated to be the main pathway for nutrition to the intervertebral disc. However, it is still a controversial issue on whether the blocking of the endplate nutritional pathway could result in intervertebral disc degeneration (IDD) in animal models. T...

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Autores principales: Yin, Si, Du, Heng, Zhao, Weigong, Ma, Shaohui, Zhang, Ming, Guan, Min, Liu, Miao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521378/
https://www.ncbi.nlm.nih.gov/pubmed/31096992
http://dx.doi.org/10.1186/s13018-019-1188-8
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author Yin, Si
Du, Heng
Zhao, Weigong
Ma, Shaohui
Zhang, Ming
Guan, Min
Liu, Miao
author_facet Yin, Si
Du, Heng
Zhao, Weigong
Ma, Shaohui
Zhang, Ming
Guan, Min
Liu, Miao
author_sort Yin, Si
collection PubMed
description BACKGROUND: The vertebral endplate route was demonstrated to be the main pathway for nutrition to the intervertebral disc. However, it is still a controversial issue on whether the blocking of the endplate nutritional pathway could result in intervertebral disc degeneration (IDD) in animal models. The aim was therefore to investigate the effect of the inhibition of both endplate nutritional pathways by bone cement injection on the IDD in a goat model. METHODS: Two lumbar intervertebral discs (L2–3 and L3–4) in eight 24-month-old goats were blocked in both endplate nutritional pathways by cement injection, and the other two lumbar intervertebral discs (L1–2 and L4–5) remained intact as normal controls. Effective blocking area percentage in nucleus pulposus (NP) was calculated, and X-rays, magnetic resonance imaging (MRI), and histology studies were performed at 4, 12, 24, and 48 weeks after operation. RESULTS: The mean effective blocking area percentage was 60.7 ± 5.3%. Imaging examinations at the time of 48 weeks after blocking the endplate nutritional pathways showed obvious IDD, with larger disc height reduction and higher degrees of disc degeneration grading compared with the normal controls. Histological examinations including HE, Masson’s trichrome, Sirius Red, and proteoglycan stainings also confirmed the degenerative changes of the blocked discs. CONCLUSIONS: The endplate nutritional route could be inhibited by blocking both endplate pathways with cement injection in a goat model. The severe inhibition in the endplate nutritional pathways may result in IDD.
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spelling pubmed-65213782019-05-23 Inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model Yin, Si Du, Heng Zhao, Weigong Ma, Shaohui Zhang, Ming Guan, Min Liu, Miao J Orthop Surg Res Research Article BACKGROUND: The vertebral endplate route was demonstrated to be the main pathway for nutrition to the intervertebral disc. However, it is still a controversial issue on whether the blocking of the endplate nutritional pathway could result in intervertebral disc degeneration (IDD) in animal models. The aim was therefore to investigate the effect of the inhibition of both endplate nutritional pathways by bone cement injection on the IDD in a goat model. METHODS: Two lumbar intervertebral discs (L2–3 and L3–4) in eight 24-month-old goats were blocked in both endplate nutritional pathways by cement injection, and the other two lumbar intervertebral discs (L1–2 and L4–5) remained intact as normal controls. Effective blocking area percentage in nucleus pulposus (NP) was calculated, and X-rays, magnetic resonance imaging (MRI), and histology studies were performed at 4, 12, 24, and 48 weeks after operation. RESULTS: The mean effective blocking area percentage was 60.7 ± 5.3%. Imaging examinations at the time of 48 weeks after blocking the endplate nutritional pathways showed obvious IDD, with larger disc height reduction and higher degrees of disc degeneration grading compared with the normal controls. Histological examinations including HE, Masson’s trichrome, Sirius Red, and proteoglycan stainings also confirmed the degenerative changes of the blocked discs. CONCLUSIONS: The endplate nutritional route could be inhibited by blocking both endplate pathways with cement injection in a goat model. The severe inhibition in the endplate nutritional pathways may result in IDD. BioMed Central 2019-05-16 /pmc/articles/PMC6521378/ /pubmed/31096992 http://dx.doi.org/10.1186/s13018-019-1188-8 Text en © The Author(s). 2019 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
Yin, Si
Du, Heng
Zhao, Weigong
Ma, Shaohui
Zhang, Ming
Guan, Min
Liu, Miao
Inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model
title Inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model
title_full Inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model
title_fullStr Inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model
title_full_unstemmed Inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model
title_short Inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model
title_sort inhibition of both endplate nutritional pathways results in intervertebral disc degeneration in a goat model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521378/
https://www.ncbi.nlm.nih.gov/pubmed/31096992
http://dx.doi.org/10.1186/s13018-019-1188-8
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