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Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers
The purpose of this study was to compare the early or late expression levels of p65, Bcl-2, and type II myosin and the frequency of TUNEL-positive nuclei in the rat masseter muscle after injection of different concentrations of botulinum toxin-A (BTX-A). We injected either 5 U or 10 U of BTX-A into...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936988/ https://www.ncbi.nlm.nih.gov/pubmed/27398270 http://dx.doi.org/10.1186/s40064-016-2680-9 |
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author | Moon, Young-Min Kim, Min-Keun Kim, Seong-Gon Kim, Tae-Woo |
author_facet | Moon, Young-Min Kim, Min-Keun Kim, Seong-Gon Kim, Tae-Woo |
author_sort | Moon, Young-Min |
collection | PubMed |
description | The purpose of this study was to compare the early or late expression levels of p65, Bcl-2, and type II myosin and the frequency of TUNEL-positive nuclei in the rat masseter muscle after injection of different concentrations of botulinum toxin-A (BTX-A). We injected either 5 U or 10 U of BTX-A into both masseter muscles of the rat. As a control group, the same volume of saline was injected. After 2 or 12 weeks, the animals were sacrificed. Subsequently, a biopsy and immunohistochemical staining of the samples were performed using a p65, Bcl-2, or type II myosin antibody. Additionally, a TUNEL assay and transmission electron microscopic analysis were performed. The expression of p65, Bcl-2, and type II myosin increased significantly with increasing concentrations of BTX-A at 2 weeks after BTX-A injection (P < 0.05). The number of TUNEL-positive nuclei was also significantly increased in the BTX-A-treated groups in comparison to the saline-treated control at 2 weeks after BTX-A injection (P < 0.05). Elevated expression of Bcl-2 was also observed in 10-unit BTX-A-treated group at 12 weeks after injection (P < 0.05). At 12 weeks after injection, the number of enlarged mitochondria was increased, and many mitochondria displayed aberrations in cristae morphology after BTX-A injection. In conclusion, BTX-A injection into the masseter muscle increased the expression level of p65, Bcl-2, and type II myosin at an early stage. The morphological changes of mitochondria were more evident at 12 weeks after injection. |
format | Online Article Text |
id | pubmed-4936988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-49369882016-07-08 Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers Moon, Young-Min Kim, Min-Keun Kim, Seong-Gon Kim, Tae-Woo Springerplus Research The purpose of this study was to compare the early or late expression levels of p65, Bcl-2, and type II myosin and the frequency of TUNEL-positive nuclei in the rat masseter muscle after injection of different concentrations of botulinum toxin-A (BTX-A). We injected either 5 U or 10 U of BTX-A into both masseter muscles of the rat. As a control group, the same volume of saline was injected. After 2 or 12 weeks, the animals were sacrificed. Subsequently, a biopsy and immunohistochemical staining of the samples were performed using a p65, Bcl-2, or type II myosin antibody. Additionally, a TUNEL assay and transmission electron microscopic analysis were performed. The expression of p65, Bcl-2, and type II myosin increased significantly with increasing concentrations of BTX-A at 2 weeks after BTX-A injection (P < 0.05). The number of TUNEL-positive nuclei was also significantly increased in the BTX-A-treated groups in comparison to the saline-treated control at 2 weeks after BTX-A injection (P < 0.05). Elevated expression of Bcl-2 was also observed in 10-unit BTX-A-treated group at 12 weeks after injection (P < 0.05). At 12 weeks after injection, the number of enlarged mitochondria was increased, and many mitochondria displayed aberrations in cristae morphology after BTX-A injection. In conclusion, BTX-A injection into the masseter muscle increased the expression level of p65, Bcl-2, and type II myosin at an early stage. The morphological changes of mitochondria were more evident at 12 weeks after injection. Springer International Publishing 2016-07-07 /pmc/articles/PMC4936988/ /pubmed/27398270 http://dx.doi.org/10.1186/s40064-016-2680-9 Text en © The Author(s) 2016 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. |
spellingShingle | Research Moon, Young-Min Kim, Min-Keun Kim, Seong-Gon Kim, Tae-Woo Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers |
title | Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers |
title_full | Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers |
title_fullStr | Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers |
title_full_unstemmed | Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers |
title_short | Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers |
title_sort | apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936988/ https://www.ncbi.nlm.nih.gov/pubmed/27398270 http://dx.doi.org/10.1186/s40064-016-2680-9 |
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