Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1038/sj.npp.1300694 http://repositorio.unifesp.br/handle/11600/28354 |
Resumo: | Immobilization stress upregulates c-Fos expression in several CNS areas. Repeated stress or the use of drugs can modulate stress-induced c-Fos expression. Here, we investigated in 40 different areas of the rat brain the effects of dexamethasone (SDX, a synthetic glucocorticoid), diazepam (SBDZ, a benzodiazepine), and imipramine (IMI, an antidepressant) on the c-Fos expression induced by restraint stress. Wistar rats were divided into four groups and submitted to 20 days of daily injection of saline (three first groups) or imipramine, 15 mg/kg, i.p. On day 21, animals were submitted to injections of saline (somatosensory, SS), SDX (1 mg/kg, i.p.), SBDZ (5 mg/kg, i.p.), or IMI (15 mg/kg, i.p.) before being submitted to restraint. Immediately after stress, the animals were perfused and their brains processed with immunohistochemistry for c-Fos (Ab-5 Oncogene Science). Dexamethasone reduced stress- induced c-Fos expression in SS cortex, hippocampus, paraventricular nucleus of the hypothalamus (PVH), and locus coeruleus (LC), whereas diazepam reduced c-Fos staining in the SS cortex, hippocampus, bed nucleus of stria terminalis, septal area, and hypothalamus (preoptic area and supramammillary nucleus). Chronic administration of imipramine decreased staining in the hippocampus, PVH, and LC, while increasing it in the nucleus raphe pallidus. We conclude that dexamethasone, diazepam and imipramine differentially modulate stress-induced Fos expression. the present study provides an important comparative background that may help in the further understanding of the effects of these compounds and on the brain activation as well as on the behavioral, neuroendocrine, and autonomic responses to stress. |
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Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramineimmediate-early genesc-Fosrestraint stressantidepressantsglucocorticoidsbenzodiazepinesImmobilization stress upregulates c-Fos expression in several CNS areas. Repeated stress or the use of drugs can modulate stress-induced c-Fos expression. Here, we investigated in 40 different areas of the rat brain the effects of dexamethasone (SDX, a synthetic glucocorticoid), diazepam (SBDZ, a benzodiazepine), and imipramine (IMI, an antidepressant) on the c-Fos expression induced by restraint stress. Wistar rats were divided into four groups and submitted to 20 days of daily injection of saline (three first groups) or imipramine, 15 mg/kg, i.p. On day 21, animals were submitted to injections of saline (somatosensory, SS), SDX (1 mg/kg, i.p.), SBDZ (5 mg/kg, i.p.), or IMI (15 mg/kg, i.p.) before being submitted to restraint. Immediately after stress, the animals were perfused and their brains processed with immunohistochemistry for c-Fos (Ab-5 Oncogene Science). Dexamethasone reduced stress- induced c-Fos expression in SS cortex, hippocampus, paraventricular nucleus of the hypothalamus (PVH), and locus coeruleus (LC), whereas diazepam reduced c-Fos staining in the SS cortex, hippocampus, bed nucleus of stria terminalis, septal area, and hypothalamus (preoptic area and supramammillary nucleus). Chronic administration of imipramine decreased staining in the hippocampus, PVH, and LC, while increasing it in the nucleus raphe pallidus. We conclude that dexamethasone, diazepam and imipramine differentially modulate stress-induced Fos expression. the present study provides an important comparative background that may help in the further understanding of the effects of these compounds and on the brain activation as well as on the behavioral, neuroendocrine, and autonomic responses to stress.UFRRJ, Dept Physiol Sci, BR-23890000 Rio de Janeiro, BrazilUniversidade Federal de São Paulo, Dept Physiol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Psychobiol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Physiol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Psychobiol, São Paulo, BrazilWeb of ScienceNature Publishing GroupUFRRJUniversidade Federal de São Paulo (UNIFESP)Medeiros, Magda Alves deReis, Luis CarlosMello, Luiz Eugênio Araujo de Moraes [UNIFESP]2016-01-24T12:37:55Z2016-01-24T12:37:55Z2005-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1246-1256http://dx.doi.org/10.1038/sj.npp.1300694Neuropsychopharmacology. London: Nature Publishing Group, v. 30, n. 7, p. 1246-1256, 2005.10.1038/sj.npp.13006940893-133Xhttp://repositorio.unifesp.br/handle/11600/28354WOS:000229881800003engNeuropsychopharmacologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-09-27T10:14:41Zoai:repositorio.unifesp.br/:11600/28354Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-09-27T10:14:41Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine |
title |
Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine |
spellingShingle |
Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine Medeiros, Magda Alves de immediate-early genes c-Fos restraint stress antidepressants glucocorticoids benzodiazepines |
title_short |
Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine |
title_full |
Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine |
title_fullStr |
Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine |
title_full_unstemmed |
Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine |
title_sort |
Stress-induced c-Fos expression is differentially modulated by dexamethasone, diazepam and imipramine |
author |
Medeiros, Magda Alves de |
author_facet |
Medeiros, Magda Alves de Reis, Luis Carlos Mello, Luiz Eugênio Araujo de Moraes [UNIFESP] |
author_role |
author |
author2 |
Reis, Luis Carlos Mello, Luiz Eugênio Araujo de Moraes [UNIFESP] |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
UFRRJ Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Medeiros, Magda Alves de Reis, Luis Carlos Mello, Luiz Eugênio Araujo de Moraes [UNIFESP] |
dc.subject.por.fl_str_mv |
immediate-early genes c-Fos restraint stress antidepressants glucocorticoids benzodiazepines |
topic |
immediate-early genes c-Fos restraint stress antidepressants glucocorticoids benzodiazepines |
description |
Immobilization stress upregulates c-Fos expression in several CNS areas. Repeated stress or the use of drugs can modulate stress-induced c-Fos expression. Here, we investigated in 40 different areas of the rat brain the effects of dexamethasone (SDX, a synthetic glucocorticoid), diazepam (SBDZ, a benzodiazepine), and imipramine (IMI, an antidepressant) on the c-Fos expression induced by restraint stress. Wistar rats were divided into four groups and submitted to 20 days of daily injection of saline (three first groups) or imipramine, 15 mg/kg, i.p. On day 21, animals were submitted to injections of saline (somatosensory, SS), SDX (1 mg/kg, i.p.), SBDZ (5 mg/kg, i.p.), or IMI (15 mg/kg, i.p.) before being submitted to restraint. Immediately after stress, the animals were perfused and their brains processed with immunohistochemistry for c-Fos (Ab-5 Oncogene Science). Dexamethasone reduced stress- induced c-Fos expression in SS cortex, hippocampus, paraventricular nucleus of the hypothalamus (PVH), and locus coeruleus (LC), whereas diazepam reduced c-Fos staining in the SS cortex, hippocampus, bed nucleus of stria terminalis, septal area, and hypothalamus (preoptic area and supramammillary nucleus). Chronic administration of imipramine decreased staining in the hippocampus, PVH, and LC, while increasing it in the nucleus raphe pallidus. We conclude that dexamethasone, diazepam and imipramine differentially modulate stress-induced Fos expression. the present study provides an important comparative background that may help in the further understanding of the effects of these compounds and on the brain activation as well as on the behavioral, neuroendocrine, and autonomic responses to stress. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-07-01 2016-01-24T12:37:55Z 2016-01-24T12:37:55Z |
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/10.1038/sj.npp.1300694 Neuropsychopharmacology. London: Nature Publishing Group, v. 30, n. 7, p. 1246-1256, 2005. 10.1038/sj.npp.1300694 0893-133X http://repositorio.unifesp.br/handle/11600/28354 WOS:000229881800003 |
url |
http://dx.doi.org/10.1038/sj.npp.1300694 http://repositorio.unifesp.br/handle/11600/28354 |
identifier_str_mv |
Neuropsychopharmacology. London: Nature Publishing Group, v. 30, n. 7, p. 1246-1256, 2005. 10.1038/sj.npp.1300694 0893-133X WOS:000229881800003 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Neuropsychopharmacology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1246-1256 |
dc.publisher.none.fl_str_mv |
Nature Publishing Group |
publisher.none.fl_str_mv |
Nature Publishing Group |
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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1814268308543766528 |