Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1016/j.brainres.2012.09.021 http://repositorio.unifesp.br/handle/11600/35500 |
Resumo: | Lack of dystrophin in Duchenne muscle dystrophy (DMD) and in the mutant mdx mouse results in progressive muscle degeneration, structural changes at the neuromuscular junction, and destabilization of the nicotinic acetylcholine receptors (nAChRs). One-third of DMD patients also present non-progressive cognitive impairments. Considering the role of the cholinergic system in cognitive functions, the number of nAChR binding sites and the mRNA levels of alpha 4, beta 2, and alpha 7 subunits were determined in brain regions normally enriched in dystrophin (cortex, hippocampus and cerebellum) of mdx mice using specific ligands and reverse-transcription polymerase chain reaction assays, respectively. Membrane preparations of these brain regions were obtained from male control and mdx mice at 4 and 12 months of age. the number of [H-3]-cytisine (alpha 4 beta 2) and [I-125]-alpha-bungarotoxin ([I-125]-alpha BGT, alpha 7) binding sites in the cortex and cerebellum was not altered with age or among age-matched control and mdx mice. A significant reduction in [H-3]-cytisine (48%) and [I-125]-alpha BGT (37%) binding sites was detected in the hippocampus of mdx mice at 12 months of age. When compared with the age-matched control groups, the mdx mice did not have significantly altered [H-3]-cytisine binding in the hippocampus, but [I-125]-alpha BGT binding in the same brain region was 52% higher at 4 months and 20% lower at 12 months. mRNA transcripts for the nAChR alpha 4, beta 2, and alpha 7 subunits were not significantly altered in the same brain regions of all animal groups. These results suggest a potential alteration of the nicotinic cholinergic function in the hippocampus of dystrophin-deficient mice, which might contribute to the impairments in cognitive functions, such as learning and memory, that have been reported in the dystrophic murine model and DMD patients. (C) 2012 Elsevier B.V. All rights reserved. |
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Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient miceNicotinic acetylcholine receptorDystrophinHippocampusMemorymdx mouseDuchenne muscle dystrophyLack of dystrophin in Duchenne muscle dystrophy (DMD) and in the mutant mdx mouse results in progressive muscle degeneration, structural changes at the neuromuscular junction, and destabilization of the nicotinic acetylcholine receptors (nAChRs). One-third of DMD patients also present non-progressive cognitive impairments. Considering the role of the cholinergic system in cognitive functions, the number of nAChR binding sites and the mRNA levels of alpha 4, beta 2, and alpha 7 subunits were determined in brain regions normally enriched in dystrophin (cortex, hippocampus and cerebellum) of mdx mice using specific ligands and reverse-transcription polymerase chain reaction assays, respectively. Membrane preparations of these brain regions were obtained from male control and mdx mice at 4 and 12 months of age. the number of [H-3]-cytisine (alpha 4 beta 2) and [I-125]-alpha-bungarotoxin ([I-125]-alpha BGT, alpha 7) binding sites in the cortex and cerebellum was not altered with age or among age-matched control and mdx mice. A significant reduction in [H-3]-cytisine (48%) and [I-125]-alpha BGT (37%) binding sites was detected in the hippocampus of mdx mice at 12 months of age. When compared with the age-matched control groups, the mdx mice did not have significantly altered [H-3]-cytisine binding in the hippocampus, but [I-125]-alpha BGT binding in the same brain region was 52% higher at 4 months and 20% lower at 12 months. mRNA transcripts for the nAChR alpha 4, beta 2, and alpha 7 subunits were not significantly altered in the same brain regions of all animal groups. These results suggest a potential alteration of the nicotinic cholinergic function in the hippocampus of dystrophin-deficient mice, which might contribute to the impairments in cognitive functions, such as learning and memory, that have been reported in the dystrophic murine model and DMD patients. (C) 2012 Elsevier B.V. All rights reserved.Universidade Federal de São Paulo, Escola Paulista Med, Sect Nat Prod, Dept Pharmacol, São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Sect Expt Endocrinol, Dept Pharmacol, São Paulo, BrazilUniv Fed Santa Catarina, Dept Pharmacol, Neuropharmacol Lab, Florianopolis, SC, BrazilAmazon Biotechnol Ctr, Lab Pharmacol & Toxicol, Manaus, AM, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Sect Nat Prod, Dept Pharmacol, São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Sect Expt Endocrinol, Dept Pharmacol, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Elsevier B.V.Universidade Federal de São Paulo (UNIFESP)Universidade Federal de Santa Catarina (UFSC)Amazon Biotechnol CtrGhedini, Paulo César [UNIFESP]Avellar, Maria Christina Werneck [UNIFESP]Lima, Thereza Cristina Monteiro deLima-Landman, Maria Teresa Riggio de [UNIFESP]Lapa, Antonio José [UNIFESP]Souccar, Caden [UNIFESP]2016-01-24T14:28:00Z2016-01-24T14:28:00Z2012-11-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion96-104application/pdfhttp://dx.doi.org/10.1016/j.brainres.2012.09.021Brain Research. Amsterdam: Elsevier B.V., v. 1483, p. 96-104, 2012.10.1016/j.brainres.2012.09.021WOS000311174900011.pdf0006-8993http://repositorio.unifesp.br/handle/11600/35500WOS:000311174900011engBrain Researchinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T16:01:15Zoai:repositorio.unifesp.br/:11600/35500Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T16:01:15Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice |
title |
Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice |
spellingShingle |
Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice Ghedini, Paulo César [UNIFESP] Nicotinic acetylcholine receptor Dystrophin Hippocampus Memory mdx mouse Duchenne muscle dystrophy |
title_short |
Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice |
title_full |
Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice |
title_fullStr |
Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice |
title_full_unstemmed |
Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice |
title_sort |
Quantitative changes of nicotinic receptors in the hippocampus of dystrophin-deficient mice |
author |
Ghedini, Paulo César [UNIFESP] |
author_facet |
Ghedini, Paulo César [UNIFESP] Avellar, Maria Christina Werneck [UNIFESP] Lima, Thereza Cristina Monteiro de Lima-Landman, Maria Teresa Riggio de [UNIFESP] Lapa, Antonio José [UNIFESP] Souccar, Caden [UNIFESP] |
author_role |
author |
author2 |
Avellar, Maria Christina Werneck [UNIFESP] Lima, Thereza Cristina Monteiro de Lima-Landman, Maria Teresa Riggio de [UNIFESP] Lapa, Antonio José [UNIFESP] Souccar, Caden [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Universidade Federal de Santa Catarina (UFSC) Amazon Biotechnol Ctr |
dc.contributor.author.fl_str_mv |
Ghedini, Paulo César [UNIFESP] Avellar, Maria Christina Werneck [UNIFESP] Lima, Thereza Cristina Monteiro de Lima-Landman, Maria Teresa Riggio de [UNIFESP] Lapa, Antonio José [UNIFESP] Souccar, Caden [UNIFESP] |
dc.subject.por.fl_str_mv |
Nicotinic acetylcholine receptor Dystrophin Hippocampus Memory mdx mouse Duchenne muscle dystrophy |
topic |
Nicotinic acetylcholine receptor Dystrophin Hippocampus Memory mdx mouse Duchenne muscle dystrophy |
description |
Lack of dystrophin in Duchenne muscle dystrophy (DMD) and in the mutant mdx mouse results in progressive muscle degeneration, structural changes at the neuromuscular junction, and destabilization of the nicotinic acetylcholine receptors (nAChRs). One-third of DMD patients also present non-progressive cognitive impairments. Considering the role of the cholinergic system in cognitive functions, the number of nAChR binding sites and the mRNA levels of alpha 4, beta 2, and alpha 7 subunits were determined in brain regions normally enriched in dystrophin (cortex, hippocampus and cerebellum) of mdx mice using specific ligands and reverse-transcription polymerase chain reaction assays, respectively. Membrane preparations of these brain regions were obtained from male control and mdx mice at 4 and 12 months of age. the number of [H-3]-cytisine (alpha 4 beta 2) and [I-125]-alpha-bungarotoxin ([I-125]-alpha BGT, alpha 7) binding sites in the cortex and cerebellum was not altered with age or among age-matched control and mdx mice. A significant reduction in [H-3]-cytisine (48%) and [I-125]-alpha BGT (37%) binding sites was detected in the hippocampus of mdx mice at 12 months of age. When compared with the age-matched control groups, the mdx mice did not have significantly altered [H-3]-cytisine binding in the hippocampus, but [I-125]-alpha BGT binding in the same brain region was 52% higher at 4 months and 20% lower at 12 months. mRNA transcripts for the nAChR alpha 4, beta 2, and alpha 7 subunits were not significantly altered in the same brain regions of all animal groups. These results suggest a potential alteration of the nicotinic cholinergic function in the hippocampus of dystrophin-deficient mice, which might contribute to the impairments in cognitive functions, such as learning and memory, that have been reported in the dystrophic murine model and DMD patients. (C) 2012 Elsevier B.V. All rights reserved. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-11-05 2016-01-24T14:28:00Z 2016-01-24T14:28:00Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.brainres.2012.09.021 Brain Research. Amsterdam: Elsevier B.V., v. 1483, p. 96-104, 2012. 10.1016/j.brainres.2012.09.021 WOS000311174900011.pdf 0006-8993 http://repositorio.unifesp.br/handle/11600/35500 WOS:000311174900011 |
url |
http://dx.doi.org/10.1016/j.brainres.2012.09.021 http://repositorio.unifesp.br/handle/11600/35500 |
identifier_str_mv |
Brain Research. Amsterdam: Elsevier B.V., v. 1483, p. 96-104, 2012. 10.1016/j.brainres.2012.09.021 WOS000311174900011.pdf 0006-8993 WOS:000311174900011 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brain Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
dc.format.none.fl_str_mv |
96-104 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268276324171776 |