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Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model
Dystonia is a neurological disorder characterized by excessive involuntary muscle contractions that lead to twisting movements. The exaggerated movements have been studied and have implicated basal ganglia as the point of origin. In more recent studies, the cerebellum has also been identified as the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Leibniz Research Centre for Working Environment and Human Factors
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318686/ https://www.ncbi.nlm.nih.gov/pubmed/28337103 http://dx.doi.org/10.17179/excli2016-482 |
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author | Wang, Tsui-chin Ngampramuan, Sukonthar Kotchabhakdi, Naiphinich |
author_facet | Wang, Tsui-chin Ngampramuan, Sukonthar Kotchabhakdi, Naiphinich |
author_sort | Wang, Tsui-chin |
collection | PubMed |
description | Dystonia is a neurological disorder characterized by excessive involuntary muscle contractions that lead to twisting movements. The exaggerated movements have been studied and have implicated basal ganglia as the point of origin. In more recent studies, the cerebellum has also been identified as the possible target of dystonia, in the search for alternative treatments. Tiagabine is a selective GABA transporter inhibitor, which blocks the reuptake and recycling of GABA. The study of GABAergic drugs as an alternative treatment for cerebellar induced dystonia has not been reported. In our study, tiagabine was i.p. injected into kainic acid induced, cerebellar dystonic adult rats, and the effects were compared with non-tiagabine injected and sham-operated groups. Beam walking apparatus, telemetric electromyography (EMG) recording, and histological verification were performed to confirm dystonic symptoms in the rats on post-surgery treatment. Involuntary dystonic spasm was observed with repetitive rigidity, and twisting movements in the rats were also confirmed by a high score on the dystonic scoring and a high amplitude on the EMG data. The rats with tiagabine treatment were scored based on motor amelioration assessed via beam walking. The result of this study suggests and confirms that low dose of kainic acid microinjection is sufficient to induce dystonia from the cerebellar vermis. In addition, from the results of the EMG recording and the behavioral assessment through beam walking, tiagabine is demonstrated as being effective in reducing dystonic spasm and may be a possible alternative therapeutic drug in the treatment of dystonia. |
format | Online Article Text |
id | pubmed-5318686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Leibniz Research Centre for Working Environment and Human Factors |
record_format | MEDLINE/PubMed |
spelling | pubmed-53186862017-03-23 Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model Wang, Tsui-chin Ngampramuan, Sukonthar Kotchabhakdi, Naiphinich EXCLI J Original Article Dystonia is a neurological disorder characterized by excessive involuntary muscle contractions that lead to twisting movements. The exaggerated movements have been studied and have implicated basal ganglia as the point of origin. In more recent studies, the cerebellum has also been identified as the possible target of dystonia, in the search for alternative treatments. Tiagabine is a selective GABA transporter inhibitor, which blocks the reuptake and recycling of GABA. The study of GABAergic drugs as an alternative treatment for cerebellar induced dystonia has not been reported. In our study, tiagabine was i.p. injected into kainic acid induced, cerebellar dystonic adult rats, and the effects were compared with non-tiagabine injected and sham-operated groups. Beam walking apparatus, telemetric electromyography (EMG) recording, and histological verification were performed to confirm dystonic symptoms in the rats on post-surgery treatment. Involuntary dystonic spasm was observed with repetitive rigidity, and twisting movements in the rats were also confirmed by a high score on the dystonic scoring and a high amplitude on the EMG data. The rats with tiagabine treatment were scored based on motor amelioration assessed via beam walking. The result of this study suggests and confirms that low dose of kainic acid microinjection is sufficient to induce dystonia from the cerebellar vermis. In addition, from the results of the EMG recording and the behavioral assessment through beam walking, tiagabine is demonstrated as being effective in reducing dystonic spasm and may be a possible alternative therapeutic drug in the treatment of dystonia. Leibniz Research Centre for Working Environment and Human Factors 2016-11-17 /pmc/articles/PMC5318686/ /pubmed/28337103 http://dx.doi.org/10.17179/excli2016-482 Text en Copyright © 2016 Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited. |
spellingShingle | Original Article Wang, Tsui-chin Ngampramuan, Sukonthar Kotchabhakdi, Naiphinich Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model |
title | Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model |
title_full | Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model |
title_fullStr | Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model |
title_full_unstemmed | Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model |
title_short | Tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model |
title_sort | tiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318686/ https://www.ncbi.nlm.nih.gov/pubmed/28337103 http://dx.doi.org/10.17179/excli2016-482 |
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