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Study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration
OBJECTIVE: In the present work we studied the expression of nerve growth associated protein (GAP-43) in a rat model of intervertebral disc degeneration. METHODS: 16 healthy adult SD rats, male or female, with an average weight 220g were selected. FluoroGold was injected in L5-L6 disc as the tracer....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Society of Musculoskeletal and Neuronal Interactions
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492325/ https://www.ncbi.nlm.nih.gov/pubmed/28574417 |
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author | Jiang, H. Wang, J. Xu, B. Yang, Q. Liu, Y. |
author_facet | Jiang, H. Wang, J. Xu, B. Yang, Q. Liu, Y. |
author_sort | Jiang, H. |
collection | PubMed |
description | OBJECTIVE: In the present work we studied the expression of nerve growth associated protein (GAP-43) in a rat model of intervertebral disc degeneration. METHODS: 16 healthy adult SD rats, male or female, with an average weight 220g were selected. FluoroGold was injected in L5-L6 disc as the tracer. After 7 days, Freund’s adjuvant was then injected to build model of intervertebral disc degeneration. After 1, 3, 7 and 14 days of modeling immune-histochemical method was used to detect the T13-L6 dorsal root ganglion and positive expression of GAP-43, TNF-α and IL-1 in L5-L6 intervertebral disc; RT-PCR method was used to detect GAP-43 mRNA and Western blot method was utilized to detect the expression levels of protein. RESULTS: In the observation group, the dorsal root ganglion, positive expression rates of GAP-43, TNF-α and IL-1, expression levels of GAP-43 mRNA and protein in the intervertebral disc at each time point were significantly higher than those in the control group, and the differences were statistically significant (P<0.05); the positive expression rates of GAP-43, TNF-α and IL-1, expression levels of GAP-43 mRNA and protein of the observation group reached the peak at 3d, and dropped at 7d; dorsal root ganglion reached the peak at 7d and dropped at 14d. CONCLUSION: Degenerative changes might be mediated by the abnormal high expression of GAP-43 and intervertebral disc inflammation jointly. |
format | Online Article Text |
id | pubmed-5492325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Society of Musculoskeletal and Neuronal Interactions |
record_format | MEDLINE/PubMed |
spelling | pubmed-54923252017-07-05 Study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration Jiang, H. Wang, J. Xu, B. Yang, Q. Liu, Y. J Musculoskelet Neuronal Interact Original Article OBJECTIVE: In the present work we studied the expression of nerve growth associated protein (GAP-43) in a rat model of intervertebral disc degeneration. METHODS: 16 healthy adult SD rats, male or female, with an average weight 220g were selected. FluoroGold was injected in L5-L6 disc as the tracer. After 7 days, Freund’s adjuvant was then injected to build model of intervertebral disc degeneration. After 1, 3, 7 and 14 days of modeling immune-histochemical method was used to detect the T13-L6 dorsal root ganglion and positive expression of GAP-43, TNF-α and IL-1 in L5-L6 intervertebral disc; RT-PCR method was used to detect GAP-43 mRNA and Western blot method was utilized to detect the expression levels of protein. RESULTS: In the observation group, the dorsal root ganglion, positive expression rates of GAP-43, TNF-α and IL-1, expression levels of GAP-43 mRNA and protein in the intervertebral disc at each time point were significantly higher than those in the control group, and the differences were statistically significant (P<0.05); the positive expression rates of GAP-43, TNF-α and IL-1, expression levels of GAP-43 mRNA and protein of the observation group reached the peak at 3d, and dropped at 7d; dorsal root ganglion reached the peak at 7d and dropped at 14d. CONCLUSION: Degenerative changes might be mediated by the abnormal high expression of GAP-43 and intervertebral disc inflammation jointly. International Society of Musculoskeletal and Neuronal Interactions 2017-06 /pmc/articles/PMC5492325/ /pubmed/28574417 Text en Copyright: © Journal of Musculoskeletal and Neuronal Interactions http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jiang, H. Wang, J. Xu, B. Yang, Q. Liu, Y. Study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration |
title | Study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration |
title_full | Study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration |
title_fullStr | Study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration |
title_full_unstemmed | Study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration |
title_short | Study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration |
title_sort | study on the expression of nerve growth associated protein-43 in rat model of intervertebral disc degeneration |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492325/ https://www.ncbi.nlm.nih.gov/pubmed/28574417 |
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