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In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey

BACKGROUND: Recently, biological therapies for early intervention of degenerative disc disease have been introduced and developed; however, a functional animal model that mimics slowly progressive disc degeneration of humans does not exist. The objective of this study was to establish a slowly progr...

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Autores principales: Wei, Fuxin, Zhong, Rui, Zhou, Zhiyu, Wang, Le, Pan, Ximin, Cui, Shangbin, Zou, Xuenong, Gao, Manman, Sun, Haixing, Chen, Wenfang, Liu, Shaoyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210630/
https://www.ncbi.nlm.nih.gov/pubmed/25298000
http://dx.doi.org/10.1186/1471-2474-15-340
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author Wei, Fuxin
Zhong, Rui
Zhou, Zhiyu
Wang, Le
Pan, Ximin
Cui, Shangbin
Zou, Xuenong
Gao, Manman
Sun, Haixing
Chen, Wenfang
Liu, Shaoyu
author_facet Wei, Fuxin
Zhong, Rui
Zhou, Zhiyu
Wang, Le
Pan, Ximin
Cui, Shangbin
Zou, Xuenong
Gao, Manman
Sun, Haixing
Chen, Wenfang
Liu, Shaoyu
author_sort Wei, Fuxin
collection PubMed
description BACKGROUND: Recently, biological therapies for early intervention of degenerative disc disease have been introduced and developed; however, a functional animal model that mimics slowly progressive disc degeneration of humans does not exist. The objective of this study was to establish a slowly progressive and reproducible intervertebral disc (IVD) degeneration model. METHODS: The subchondral bone adjacent to the lumbar IVDs (L3/4 and L5/6) of ten rhesus monkeys was randomly injected with 4 ml bleomycin solution (1.5 mg/ml), or 4 ml phosphate buffer saline (PBS) per segment as control, respectively. The degenerative process was investigated by using radiography and T1ρ MR imaging at 1, 3, 6, 9, 12 and 15 months postoperatively. Histological scoring, Sulfated Glycosaminoglycans (GAGs) analysis and real-time PCR were performed at 15 months. The correlation between histological score, GAGs and T1ρ values were also analyzed. RESULTS: The results showed that the mean T1ρ values of nucleus pulposus (NP) and annulus fibrosus (AF) in the bleomycin group significantly decreased after 3 and 6 months respectively, followed by slowly decrease until at 15 months. At 15 months, the histological scores was significantly higher, and the GAGs of NP was significantly lower in the bleomycin group, compared with the control group (P < 0.05). The results of real-time PCR revealed a significant increase in matrix metalloprotease (MMP)-3, A disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS)-5, tumor necrosis factor α, interleukin-1β, interleukin-6 expressions, transforming growth factor (TGF-β1) and marked reduction in aggrecan, type II collagen, von willebrand factor (vWF) expressions at the mRNA levels in the bleomycin group. Spearman correlation analysis showed a strong positive correlation between GAGs and T1ρ values of NP (r =0.740, P < 0.01), and a significant inverse correlation between histological score and T1ρ values of NP and AF (r = -0.761, r = -0.729, respectively, P < 0.01). CONCLUSIONS: Injection of bleomycin into the subchondral bone adjacent to the lumbar IVDs of rhesus monkeys can results in mild, slowly progressive disc degeneration, which mimics the onset of human disc degeneration. T1ρ MR imaging is an effective and noninvasive technique for assessment of early stage disc degeneration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2474-15-340) contains supplementary material, which is available to authorized users.
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spelling pubmed-42106302014-10-29 In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey Wei, Fuxin Zhong, Rui Zhou, Zhiyu Wang, Le Pan, Ximin Cui, Shangbin Zou, Xuenong Gao, Manman Sun, Haixing Chen, Wenfang Liu, Shaoyu BMC Musculoskelet Disord Research Article BACKGROUND: Recently, biological therapies for early intervention of degenerative disc disease have been introduced and developed; however, a functional animal model that mimics slowly progressive disc degeneration of humans does not exist. The objective of this study was to establish a slowly progressive and reproducible intervertebral disc (IVD) degeneration model. METHODS: The subchondral bone adjacent to the lumbar IVDs (L3/4 and L5/6) of ten rhesus monkeys was randomly injected with 4 ml bleomycin solution (1.5 mg/ml), or 4 ml phosphate buffer saline (PBS) per segment as control, respectively. The degenerative process was investigated by using radiography and T1ρ MR imaging at 1, 3, 6, 9, 12 and 15 months postoperatively. Histological scoring, Sulfated Glycosaminoglycans (GAGs) analysis and real-time PCR were performed at 15 months. The correlation between histological score, GAGs and T1ρ values were also analyzed. RESULTS: The results showed that the mean T1ρ values of nucleus pulposus (NP) and annulus fibrosus (AF) in the bleomycin group significantly decreased after 3 and 6 months respectively, followed by slowly decrease until at 15 months. At 15 months, the histological scores was significantly higher, and the GAGs of NP was significantly lower in the bleomycin group, compared with the control group (P < 0.05). The results of real-time PCR revealed a significant increase in matrix metalloprotease (MMP)-3, A disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS)-5, tumor necrosis factor α, interleukin-1β, interleukin-6 expressions, transforming growth factor (TGF-β1) and marked reduction in aggrecan, type II collagen, von willebrand factor (vWF) expressions at the mRNA levels in the bleomycin group. Spearman correlation analysis showed a strong positive correlation between GAGs and T1ρ values of NP (r =0.740, P < 0.01), and a significant inverse correlation between histological score and T1ρ values of NP and AF (r = -0.761, r = -0.729, respectively, P < 0.01). CONCLUSIONS: Injection of bleomycin into the subchondral bone adjacent to the lumbar IVDs of rhesus monkeys can results in mild, slowly progressive disc degeneration, which mimics the onset of human disc degeneration. T1ρ MR imaging is an effective and noninvasive technique for assessment of early stage disc degeneration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2474-15-340) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-09 /pmc/articles/PMC4210630/ /pubmed/25298000 http://dx.doi.org/10.1186/1471-2474-15-340 Text en © Wei et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Wei, Fuxin
Zhong, Rui
Zhou, Zhiyu
Wang, Le
Pan, Ximin
Cui, Shangbin
Zou, Xuenong
Gao, Manman
Sun, Haixing
Chen, Wenfang
Liu, Shaoyu
In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey
title In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey
title_full In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey
title_fullStr In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey
title_full_unstemmed In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey
title_short In vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey
title_sort in vivo experimental intervertebral disc degeneration induced by bleomycin in the rhesus monkey
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210630/
https://www.ncbi.nlm.nih.gov/pubmed/25298000
http://dx.doi.org/10.1186/1471-2474-15-340
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