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Effects of GABAa receptor antagonists on motor behavior in pharmacological Parkinson's disease model in mice
The aim of this study was to evaluate the effects of two gamma‐amino butyric acid (GABA)a receptor antagonists on motor behavioral tasks in a pharmacological model of Parkinson disease (PD) in rodents. Ninety‐six Swiss mice received intraperitoneal injection of Haloperidol (1 mg/kg) to block dopamin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371543/ https://www.ncbi.nlm.nih.gov/pubmed/28351968 http://dx.doi.org/10.14814/phy2.13081 |
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author | Mograbi, Karla De Michelis de Castro, Ana Carolini Ferreira de Oliveira, Jainny Aniely Rocha Sales, Patrick Jean Barbosa Covolan, Luciene Del Bel, Eliane Aparecida de Souza, Albert Schiaveto |
author_facet | Mograbi, Karla De Michelis de Castro, Ana Carolini Ferreira de Oliveira, Jainny Aniely Rocha Sales, Patrick Jean Barbosa Covolan, Luciene Del Bel, Eliane Aparecida de Souza, Albert Schiaveto |
author_sort | Mograbi, Karla De Michelis |
collection | PubMed |
description | The aim of this study was to evaluate the effects of two gamma‐amino butyric acid (GABA)a receptor antagonists on motor behavioral tasks in a pharmacological model of Parkinson disease (PD) in rodents. Ninety‐six Swiss mice received intraperitoneal injection of Haloperidol (1 mg/kg) to block dopaminergic receptors. GABAa receptors antagonists Bicuculline (1 and 5 mg/kg) and Flumazenil (3 and 6 mg/kg) were used for the assessment of the interaction among these neurotransmitters, in this PD model. The motor behavior of the animals was evaluated in the catalepsy test (30, 60, and 90 min after drugs application), through open field test (after 60 min) and trough functional gait assessment (after 60 min). Both Bicuculline and Flumazenil were able to partially reverse catalepsy induced by Haloperidol. In the open field test, Haloperidol reduced the number of horizontal and vertical exploration of the animals, which was not reversed trough application of GABAa antagonists. Furthermore, the functional gait assessment was not sensitive enough to detect motor changes in this animal model of PD. There is an interaction between dopamine and GABA in the basal ganglia and the blocking GABAa receptors may have therapeutic potential in the treatment of PD. |
format | Online Article Text |
id | pubmed-5371543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53715432017-03-30 Effects of GABAa receptor antagonists on motor behavior in pharmacological Parkinson's disease model in mice Mograbi, Karla De Michelis de Castro, Ana Carolini Ferreira de Oliveira, Jainny Aniely Rocha Sales, Patrick Jean Barbosa Covolan, Luciene Del Bel, Eliane Aparecida de Souza, Albert Schiaveto Physiol Rep Original Research The aim of this study was to evaluate the effects of two gamma‐amino butyric acid (GABA)a receptor antagonists on motor behavioral tasks in a pharmacological model of Parkinson disease (PD) in rodents. Ninety‐six Swiss mice received intraperitoneal injection of Haloperidol (1 mg/kg) to block dopaminergic receptors. GABAa receptors antagonists Bicuculline (1 and 5 mg/kg) and Flumazenil (3 and 6 mg/kg) were used for the assessment of the interaction among these neurotransmitters, in this PD model. The motor behavior of the animals was evaluated in the catalepsy test (30, 60, and 90 min after drugs application), through open field test (after 60 min) and trough functional gait assessment (after 60 min). Both Bicuculline and Flumazenil were able to partially reverse catalepsy induced by Haloperidol. In the open field test, Haloperidol reduced the number of horizontal and vertical exploration of the animals, which was not reversed trough application of GABAa antagonists. Furthermore, the functional gait assessment was not sensitive enough to detect motor changes in this animal model of PD. There is an interaction between dopamine and GABA in the basal ganglia and the blocking GABAa receptors may have therapeutic potential in the treatment of PD. John Wiley and Sons Inc. 2017-03-29 /pmc/articles/PMC5371543/ /pubmed/28351968 http://dx.doi.org/10.14814/phy2.13081 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Mograbi, Karla De Michelis de Castro, Ana Carolini Ferreira de Oliveira, Jainny Aniely Rocha Sales, Patrick Jean Barbosa Covolan, Luciene Del Bel, Eliane Aparecida de Souza, Albert Schiaveto Effects of GABAa receptor antagonists on motor behavior in pharmacological Parkinson's disease model in mice |
title | Effects of GABAa receptor antagonists on motor behavior in pharmacological Parkinson's disease model in mice |
title_full | Effects of GABAa receptor antagonists on motor behavior in pharmacological Parkinson's disease model in mice |
title_fullStr | Effects of GABAa receptor antagonists on motor behavior in pharmacological Parkinson's disease model in mice |
title_full_unstemmed | Effects of GABAa receptor antagonists on motor behavior in pharmacological Parkinson's disease model in mice |
title_short | Effects of GABAa receptor antagonists on motor behavior in pharmacological Parkinson's disease model in mice |
title_sort | effects of gabaa receptor antagonists on motor behavior in pharmacological parkinson's disease model in mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371543/ https://www.ncbi.nlm.nih.gov/pubmed/28351968 http://dx.doi.org/10.14814/phy2.13081 |
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