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Effect of histamine H1 and H2 receptor antagonists, microinjected into cerebellar vermis, on emotional memory consolidation in mice
This study investigated the effects of histamine H1 or H2 receptor antagonists on emotional memory consolidation in mice submitted to the elevated plus maze (EPM). The cerebellar vermis of male mice (Swiss albino) was implanted using a cannula guide. Three days after recovery, behavioral tests were...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051186/ https://www.ncbi.nlm.nih.gov/pubmed/24519129 http://dx.doi.org/10.1590/1414-431X20133429 |
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author | Gianlorenço, A.C.L. Serafim, K.R. Canto-de-Souza, A. Mattioli, R. |
author_facet | Gianlorenço, A.C.L. Serafim, K.R. Canto-de-Souza, A. Mattioli, R. |
author_sort | Gianlorenço, A.C.L. |
collection | PubMed |
description | This study investigated the effects of histamine H1 or H2 receptor antagonists on emotional memory consolidation in mice submitted to the elevated plus maze (EPM). The cerebellar vermis of male mice (Swiss albino) was implanted using a cannula guide. Three days after recovery, behavioral tests were performed in the EPM on 2 consecutive days (T1 and T2). Immediately after exposure to the EPM (T1), animals received a microinjection of saline (SAL) or the H1 antagonist chlorpheniramine (CPA; 0.016, 0.052, or 0.16 nmol/0.1 µL) in Experiment 1, and SAL or the H2 antagonist ranitidine (RA; 0.57, 2.85, or 5.7 nmol/0.1 µL) in Experiment 2. Twenty-four hours later, mice were reexposed to the EPM (T2) under the same experimental conditions but they did not receive any injection. Data were analyzed using one-way ANOVA and the Duncan test. In Experiment 1, mice microinjected with SAL and with CPA entered the open arms less often (%OAE) and spent less time in the open arms (%OAT) in T2, and there was no difference among groups. The results of Experiment 2 demonstrated that the values of %OAE and %OAT in T2 were lower compared to T1 for the groups that were microinjected with SAL and 2.85 nmol/0.1 µL RA. However, when animals were microinjected with 5.7 nmol/0.1 µL RA, they did not show a reduction in %OAE and %OAT. These results demonstrate that CPA did not affect behavior at the doses used in this study, while 5.7 nmol/0.1 µL RA induced impairment of memory consolidation in the EPM. |
format | Online Article Text |
id | pubmed-4051186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-40511862014-06-10 Effect of histamine H1 and H2 receptor antagonists, microinjected into cerebellar vermis, on emotional memory consolidation in mice Gianlorenço, A.C.L. Serafim, K.R. Canto-de-Souza, A. Mattioli, R. Braz J Med Biol Res Biomedical Sciences This study investigated the effects of histamine H1 or H2 receptor antagonists on emotional memory consolidation in mice submitted to the elevated plus maze (EPM). The cerebellar vermis of male mice (Swiss albino) was implanted using a cannula guide. Three days after recovery, behavioral tests were performed in the EPM on 2 consecutive days (T1 and T2). Immediately after exposure to the EPM (T1), animals received a microinjection of saline (SAL) or the H1 antagonist chlorpheniramine (CPA; 0.016, 0.052, or 0.16 nmol/0.1 µL) in Experiment 1, and SAL or the H2 antagonist ranitidine (RA; 0.57, 2.85, or 5.7 nmol/0.1 µL) in Experiment 2. Twenty-four hours later, mice were reexposed to the EPM (T2) under the same experimental conditions but they did not receive any injection. Data were analyzed using one-way ANOVA and the Duncan test. In Experiment 1, mice microinjected with SAL and with CPA entered the open arms less often (%OAE) and spent less time in the open arms (%OAT) in T2, and there was no difference among groups. The results of Experiment 2 demonstrated that the values of %OAE and %OAT in T2 were lower compared to T1 for the groups that were microinjected with SAL and 2.85 nmol/0.1 µL RA. However, when animals were microinjected with 5.7 nmol/0.1 µL RA, they did not show a reduction in %OAE and %OAT. These results demonstrate that CPA did not affect behavior at the doses used in this study, while 5.7 nmol/0.1 µL RA induced impairment of memory consolidation in the EPM. Associação Brasileira de Divulgação Científica 2014-02-17 /pmc/articles/PMC4051186/ /pubmed/24519129 http://dx.doi.org/10.1590/1414-431X20133429 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedical Sciences Gianlorenço, A.C.L. Serafim, K.R. Canto-de-Souza, A. Mattioli, R. Effect of histamine H1 and H2 receptor antagonists, microinjected into cerebellar vermis, on emotional memory consolidation in mice |
title | Effect of histamine H1 and H2 receptor antagonists,
microinjected into cerebellar vermis, on emotional memory consolidation in
mice |
title_full | Effect of histamine H1 and H2 receptor antagonists,
microinjected into cerebellar vermis, on emotional memory consolidation in
mice |
title_fullStr | Effect of histamine H1 and H2 receptor antagonists,
microinjected into cerebellar vermis, on emotional memory consolidation in
mice |
title_full_unstemmed | Effect of histamine H1 and H2 receptor antagonists,
microinjected into cerebellar vermis, on emotional memory consolidation in
mice |
title_short | Effect of histamine H1 and H2 receptor antagonists,
microinjected into cerebellar vermis, on emotional memory consolidation in
mice |
title_sort | effect of histamine h1 and h2 receptor antagonists,
microinjected into cerebellar vermis, on emotional memory consolidation in
mice |
topic | Biomedical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051186/ https://www.ncbi.nlm.nih.gov/pubmed/24519129 http://dx.doi.org/10.1590/1414-431X20133429 |
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