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The correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats

In this study, the pathological microvessel changes to the endplate and the degeneration of the intervertebral disc of diabetic rats were examined in order to identify the possible mechanism by which diabetes mellitus (DM) induces degeneration of the intervertebral disc. A total of 30 Sprague-Dawley...

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Autores principales: CHEN, SEN, LIAO, MEIMEI, LI, JIANPING, PENG, HAO, XIONG, MIN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570219/
https://www.ncbi.nlm.nih.gov/pubmed/23408796
http://dx.doi.org/10.3892/etm.2012.868
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author CHEN, SEN
LIAO, MEIMEI
LI, JIANPING
PENG, HAO
XIONG, MIN
author_facet CHEN, SEN
LIAO, MEIMEI
LI, JIANPING
PENG, HAO
XIONG, MIN
author_sort CHEN, SEN
collection PubMed
description In this study, the pathological microvessel changes to the endplate and the degeneration of the intervertebral disc of diabetic rats were examined in order to identify the possible mechanism by which diabetes mellitus (DM) induces degeneration of the intervertebral disc. A total of 30 Sprague-Dawley rats were randomly divided into two groups. DM was induced in one of the groups by streptozotocin (STZ) administration. The rats were sacrificed 4, 8 and 12 weeks later. Five rats from each group were sacrificed at each time interval and lumbar disc and endplate tissue were obtained from each rat. The histological changes, collagen expression, microvessel density (MVD) and apoptosis of the disc were investigated by different methods. The expression of collagen I in the diabetic DM group was higher compared to the control group at the three time points (P<0.01), in contrast to the expression of collagen II. The factor VIII-related antigen (FVIII RAg) was expressed in the control and DM groups, while its expression was relatively low in the DM group. The MVD of the DM group was smaller compared to that of the control group at the three time points (P<0.01). The apoptotic index (AI) in the diabetic group was significantly higher compared to that of the control group at the three time points (P<0.01). A negative correlation was observed between the MVD of the endplates and the notochordal cell AI in the two groups. Compared to the control group, the endplate MVD decreased and the cavity became smaller or disappeared in the diabetic rats. In conclusion, there was a negative correlation between MVD and degenerative changes of the intervertebral disc in diabetic rats.
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spelling pubmed-35702192013-02-13 The correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats CHEN, SEN LIAO, MEIMEI LI, JIANPING PENG, HAO XIONG, MIN Exp Ther Med Articles In this study, the pathological microvessel changes to the endplate and the degeneration of the intervertebral disc of diabetic rats were examined in order to identify the possible mechanism by which diabetes mellitus (DM) induces degeneration of the intervertebral disc. A total of 30 Sprague-Dawley rats were randomly divided into two groups. DM was induced in one of the groups by streptozotocin (STZ) administration. The rats were sacrificed 4, 8 and 12 weeks later. Five rats from each group were sacrificed at each time interval and lumbar disc and endplate tissue were obtained from each rat. The histological changes, collagen expression, microvessel density (MVD) and apoptosis of the disc were investigated by different methods. The expression of collagen I in the diabetic DM group was higher compared to the control group at the three time points (P<0.01), in contrast to the expression of collagen II. The factor VIII-related antigen (FVIII RAg) was expressed in the control and DM groups, while its expression was relatively low in the DM group. The MVD of the DM group was smaller compared to that of the control group at the three time points (P<0.01). The apoptotic index (AI) in the diabetic group was significantly higher compared to that of the control group at the three time points (P<0.01). A negative correlation was observed between the MVD of the endplates and the notochordal cell AI in the two groups. Compared to the control group, the endplate MVD decreased and the cavity became smaller or disappeared in the diabetic rats. In conclusion, there was a negative correlation between MVD and degenerative changes of the intervertebral disc in diabetic rats. D.A. Spandidos 2013-03 2012-12-20 /pmc/articles/PMC3570219/ /pubmed/23408796 http://dx.doi.org/10.3892/etm.2012.868 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
CHEN, SEN
LIAO, MEIMEI
LI, JIANPING
PENG, HAO
XIONG, MIN
The correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats
title The correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats
title_full The correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats
title_fullStr The correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats
title_full_unstemmed The correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats
title_short The correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats
title_sort correlation between microvessel pathological changes of the endplate and degeneration of the intervertebral disc in diabetic rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570219/
https://www.ncbi.nlm.nih.gov/pubmed/23408796
http://dx.doi.org/10.3892/etm.2012.868
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