Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , |
Tipo de documento: | Artigo de conferência |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRN |
Texto Completo: | https://repositorio.ufrn.br/jspui/handle/123456789/24381 |
Resumo: | Objectives: To investigate whether the D2 antagonist haloperidol can modulate the hippocampal expression levels of Zif-268 and phosphorylated CaMKII, two synaptic plasticity biomarkers related to memory consolidation. Methods and Results: For memory consolidation analysis, male adult mice (Mus musculus, 19-29g) separated in two groups (haloperidol 0.3 mg/kg - HALO i.p. and vehicle, n=8 per group) were submitted to two sessions of object exploration with a 24 hours inter-session interval. Drugs were injected i.p. immediately after the first exploration session. An object recognition index (exploration time of unfamiliar/ familiar objects) was obtained in the second object exploration session. The HALO group presented a significant decrease in object recognition when compared to vehicle (respectively 1.51 ± 0.11 and 2.5 ± 0.19; p=0.0007). In a separate group of animals (n=10 for HALO and 11 for vehicle), the brains were removed three hours after a single session of object exploration, and the tissue was processed for immunohistochemistry of Zif-268 and phosphorilated CaMKII. Zif-268 expression was quantified by counts of positively-labeled nuclei, and CamKII phosphorylation was quantified by densitometry, with measurements taken from the hippocampal regions CA1, CA3 and dentate gyrus. We performed student t tests for comparisons between the two groups, and the significance level was set at 0.05. No significant difference related to Zif-268 expression was observed. On the other hand, a significant reduction in CaMKII phosphorylation in the CA1 region was observed in the HALO group, when compared to the vehicle group (0.84 ± 0.05 and 1.14 ± 0.1; p=0.016). Conclusions: These results suggest that the blockade of D2 receptors can impair mnemonic systems, leading to both a decrease in the phosphorylation of CAMKII, and to behavioral changes that indicate learning impairment. |
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Aguiar, L. M.Soares, B. L.França, A. S. C.Nascimento, G. C. D.Ribeiro, Sidarta Tollendal Gomes2017-11-27T16:29:50Z2017-11-27T16:29:50Z2011-08https://repositorio.ufrn.br/jspui/handle/123456789/24381engDopamineMemory consolidationSynaptic plasticitySleepRole of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidationinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectObjectives: To investigate whether the D2 antagonist haloperidol can modulate the hippocampal expression levels of Zif-268 and phosphorylated CaMKII, two synaptic plasticity biomarkers related to memory consolidation. Methods and Results: For memory consolidation analysis, male adult mice (Mus musculus, 19-29g) separated in two groups (haloperidol 0.3 mg/kg - HALO i.p. and vehicle, n=8 per group) were submitted to two sessions of object exploration with a 24 hours inter-session interval. Drugs were injected i.p. immediately after the first exploration session. An object recognition index (exploration time of unfamiliar/ familiar objects) was obtained in the second object exploration session. The HALO group presented a significant decrease in object recognition when compared to vehicle (respectively 1.51 ± 0.11 and 2.5 ± 0.19; p=0.0007). In a separate group of animals (n=10 for HALO and 11 for vehicle), the brains were removed three hours after a single session of object exploration, and the tissue was processed for immunohistochemistry of Zif-268 and phosphorilated CaMKII. Zif-268 expression was quantified by counts of positively-labeled nuclei, and CamKII phosphorylation was quantified by densitometry, with measurements taken from the hippocampal regions CA1, CA3 and dentate gyrus. We performed student t tests for comparisons between the two groups, and the significance level was set at 0.05. No significant difference related to Zif-268 expression was observed. On the other hand, a significant reduction in CaMKII phosphorylation in the CA1 region was observed in the HALO group, when compared to the vehicle group (0.84 ± 0.05 and 1.14 ± 0.1; p=0.016). Conclusions: These results suggest that the blockade of D2 receptors can impair mnemonic systems, leading to both a decrease in the phosphorylation of CAMKII, and to behavioral changes that indicate learning impairment.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNORIGINALROLE OF DOPAMINERGIC D2 RECEPTORS IN REGULATING MOLECULAR BIOMARKERS OF NEURAL.pdfROLE OF DOPAMINERGIC D2 RECEPTORS IN REGULATING MOLECULAR BIOMARKERS OF NEURAL.pdfSidartaRibeiro_ICe_2011_ROLE OF DOPAMINERGICapplication/pdf3769350https://repositorio.ufrn.br/bitstream/123456789/24381/1/ROLE%20OF%20DOPAMINERGIC%20D2%20RECEPTORS%20IN%20REGULATING%20MOLECULAR%20BIOMARKERS%20OF%20NEURAL.pdf5e9b41df7c45402d8ef06ad9f2b78109MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.ufrn.br/bitstream/123456789/24381/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52TEXTROLE OF DOPAMINERGIC D2 RECEPTORS IN REGULATING MOLECULAR BIOMARKERS OF NEURAL.pdf.txtROLE OF DOPAMINERGIC D2 RECEPTORS IN REGULATING MOLECULAR BIOMARKERS OF NEURAL.pdf.txtExtracted texttext/plain1935792https://repositorio.ufrn.br/bitstream/123456789/24381/3/ROLE%20OF%20DOPAMINERGIC%20D2%20RECEPTORS%20IN%20REGULATING%20MOLECULAR%20BIOMARKERS%20OF%20NEURAL.pdf.txtb04d6747b52fe128568ec887532a849aMD53THUMBNAILROLE OF DOPAMINERGIC D2 RECEPTORS IN REGULATING MOLECULAR BIOMARKERS OF NEURAL.pdf.jpgROLE OF DOPAMINERGIC D2 RECEPTORS IN REGULATING MOLECULAR BIOMARKERS OF NEURAL.pdf.jpgIM Thumbnailimage/jpeg4767https://repositorio.ufrn.br/bitstream/123456789/24381/4/ROLE%20OF%20DOPAMINERGIC%20D2%20RECEPTORS%20IN%20REGULATING%20MOLECULAR%20BIOMARKERS%20OF%20NEURAL.pdf.jpg062da223f85dc0816636d565361e81bbMD54123456789/243812021-07-09 20:13:45.246oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2021-07-09T23:13:45Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false |
dc.title.pt_BR.fl_str_mv |
Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation |
title |
Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation |
spellingShingle |
Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation Aguiar, L. M. Dopamine Memory consolidation Synaptic plasticity Sleep |
title_short |
Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation |
title_full |
Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation |
title_fullStr |
Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation |
title_full_unstemmed |
Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation |
title_sort |
Role of dopaminergic D2 receptors in regulating molecular biomarkers os neural lasticity and memory consolidation |
author |
Aguiar, L. M. |
author_facet |
Aguiar, L. M. Soares, B. L. França, A. S. C. Nascimento, G. C. D. Ribeiro, Sidarta Tollendal Gomes |
author_role |
author |
author2 |
Soares, B. L. França, A. S. C. Nascimento, G. C. D. Ribeiro, Sidarta Tollendal Gomes |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Aguiar, L. M. Soares, B. L. França, A. S. C. Nascimento, G. C. D. Ribeiro, Sidarta Tollendal Gomes |
dc.subject.por.fl_str_mv |
Dopamine Memory consolidation Synaptic plasticity Sleep |
topic |
Dopamine Memory consolidation Synaptic plasticity Sleep |
description |
Objectives: To investigate whether the D2 antagonist haloperidol can modulate the hippocampal expression levels of Zif-268 and phosphorylated CaMKII, two synaptic plasticity biomarkers related to memory consolidation. Methods and Results: For memory consolidation analysis, male adult mice (Mus musculus, 19-29g) separated in two groups (haloperidol 0.3 mg/kg - HALO i.p. and vehicle, n=8 per group) were submitted to two sessions of object exploration with a 24 hours inter-session interval. Drugs were injected i.p. immediately after the first exploration session. An object recognition index (exploration time of unfamiliar/ familiar objects) was obtained in the second object exploration session. The HALO group presented a significant decrease in object recognition when compared to vehicle (respectively 1.51 ± 0.11 and 2.5 ± 0.19; p=0.0007). In a separate group of animals (n=10 for HALO and 11 for vehicle), the brains were removed three hours after a single session of object exploration, and the tissue was processed for immunohistochemistry of Zif-268 and phosphorilated CaMKII. Zif-268 expression was quantified by counts of positively-labeled nuclei, and CamKII phosphorylation was quantified by densitometry, with measurements taken from the hippocampal regions CA1, CA3 and dentate gyrus. We performed student t tests for comparisons between the two groups, and the significance level was set at 0.05. No significant difference related to Zif-268 expression was observed. On the other hand, a significant reduction in CaMKII phosphorylation in the CA1 region was observed in the HALO group, when compared to the vehicle group (0.84 ± 0.05 and 1.14 ± 0.1; p=0.016). Conclusions: These results suggest that the blockade of D2 receptors can impair mnemonic systems, leading to both a decrease in the phosphorylation of CAMKII, and to behavioral changes that indicate learning impairment. |
publishDate |
2011 |
dc.date.issued.fl_str_mv |
2011-08 |
dc.date.accessioned.fl_str_mv |
2017-11-27T16:29:50Z |
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2017-11-27T16:29:50Z |
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eng |
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eng |
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