Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model

Detalhes bibliográficos
Autor(a) principal: Armani, Fernanda [UNIFESP]
Data de Publicação: 2012
Outros Autores: Andersen, Monica L. [UNIFESP], Andreatini, Roberto, Frussa-Filho, Roberto [UNIFESP], Tufik, Sergio [UNIFESP], Fernandes Galduroz, Jose Carlos [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/34356
http://dx.doi.org/10.1111/j.1755-5949.2010.00224.x
Resumo: Background: Previous studies have suggested that manic states and sleep deprivation could contribute to the pathophysiology of bipolar disorder (BD) through protein kinase C (PKC) signaling abnormalities. Moreover, adjunctive therapy has become a standard strategy in the management of BD patients who respond poorly to current pharmacological treatments. Aim: Thus, the aim of this study was to investigate the possible involvement of PKC inhibition by tamoxifen both separately or in combination with lithium, in paradoxical sleep deprivation (PSD)-induced hyperactivity, one facet of mania-like behavior. Materials & Methods: Adult male C57BL/6J mice were randomly distributed (n = 7/group) in 24-h PSD or control groups and injected intraperitoneally (i.p.) with vehicle, lithium (50, 100, or 150 mg/kg) or tamoxifen (0.5, 1.0, or 2.0 mg/kg experiment 1). in a second experiment, mice were injected i.p. with vehicle or a combination of subeffective doses of lithium and tamoxifen. Animals were subjected to a protocol based on repetitive PSD conditions, followed by assessment of locomotion activity in the open-field task. Results: PSD significantly increased locomotor activity in both experiments. These behavioral changes were prevented by a treatment with lithium or tamoxifen, or a combined treatment with both lithium and tamoxifen. Discussion: Therefore, our findings suggest that lithium and tamoxifen exert reversal effects against PSD-induced hyperactivity in mice. Conclusion: Furthermore, tamoxifen as an adjunct to lithium therapy provides support for an alternative treatment of individuals who either do not respond adequately or cannot tolerate the adverse effects associated with therapeutic doses of lithium.
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spelling Armani, Fernanda [UNIFESP]Andersen, Monica L. [UNIFESP]Andreatini, RobertoFrussa-Filho, Roberto [UNIFESP]Tufik, Sergio [UNIFESP]Fernandes Galduroz, Jose Carlos [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Univ Fed Parana2016-01-24T14:17:36Z2016-01-24T14:17:36Z2012-01-01Cns Neuroscience & Therapeutics. Hoboken: Wiley-Blackwell, v. 18, n. 2, p. 119-125, 2012.1755-5930http://repositorio.unifesp.br/handle/11600/34356http://dx.doi.org/10.1111/j.1755-5949.2010.00224.x10.1111/j.1755-5949.2010.00224.xWOS:000300001700004Background: Previous studies have suggested that manic states and sleep deprivation could contribute to the pathophysiology of bipolar disorder (BD) through protein kinase C (PKC) signaling abnormalities. Moreover, adjunctive therapy has become a standard strategy in the management of BD patients who respond poorly to current pharmacological treatments. Aim: Thus, the aim of this study was to investigate the possible involvement of PKC inhibition by tamoxifen both separately or in combination with lithium, in paradoxical sleep deprivation (PSD)-induced hyperactivity, one facet of mania-like behavior. Materials & Methods: Adult male C57BL/6J mice were randomly distributed (n = 7/group) in 24-h PSD or control groups and injected intraperitoneally (i.p.) with vehicle, lithium (50, 100, or 150 mg/kg) or tamoxifen (0.5, 1.0, or 2.0 mg/kg experiment 1). in a second experiment, mice were injected i.p. with vehicle or a combination of subeffective doses of lithium and tamoxifen. Animals were subjected to a protocol based on repetitive PSD conditions, followed by assessment of locomotion activity in the open-field task. Results: PSD significantly increased locomotor activity in both experiments. These behavioral changes were prevented by a treatment with lithium or tamoxifen, or a combined treatment with both lithium and tamoxifen. Discussion: Therefore, our findings suggest that lithium and tamoxifen exert reversal effects against PSD-induced hyperactivity in mice. Conclusion: Furthermore, tamoxifen as an adjunct to lithium therapy provides support for an alternative treatment of individuals who either do not respond adequately or cannot tolerate the adverse effects associated with therapeutic doses of lithium.Associacao Fundo de Incentivo a Psicofarmacologia (AFIP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Universidade Federal de São Paulo UNIFESP, Dept Psicobiol, São Paulo, BrazilUniv Fed Parana, Setor Ciencias Biol, Dept Farmacol, BR-80060000 Curitiba, Parana, BrazilUniversidade Federal de São Paulo UNIFESP, Dept Farmacol, São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Dept Psicobiol, São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Dept Farmacol, São Paulo, BrazilFAPESP: 98/14303-3Web of Science119-125engWiley-BlackwellCns Neuroscience & Therapeuticshttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlinfo:eu-repo/semantics/openAccessAdjunctive therapyLithiumManiaMiceParadoxical sleep deprivationProtein kinase CTamoxifenSuccessful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Modelinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlereponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/343562021-09-30 15:48:17.306metadata only accessoai:repositorio.unifesp.br:11600/34356Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652021-09-30T18:48:17Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model
title Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model
spellingShingle Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model
Armani, Fernanda [UNIFESP]
Adjunctive therapy
Lithium
Mania
Mice
Paradoxical sleep deprivation
Protein kinase C
Tamoxifen
title_short Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model
title_full Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model
title_fullStr Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model
title_full_unstemmed Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model
title_sort Successful Combined Therapy with Tamoxifen and Lithium in a Paradoxical Sleep Deprivation-Induced Mania Model
author Armani, Fernanda [UNIFESP]
author_facet Armani, Fernanda [UNIFESP]
Andersen, Monica L. [UNIFESP]
Andreatini, Roberto
Frussa-Filho, Roberto [UNIFESP]
Tufik, Sergio [UNIFESP]
Fernandes Galduroz, Jose Carlos [UNIFESP]
author_role author
author2 Andersen, Monica L. [UNIFESP]
Andreatini, Roberto
Frussa-Filho, Roberto [UNIFESP]
Tufik, Sergio [UNIFESP]
Fernandes Galduroz, Jose Carlos [UNIFESP]
author2_role author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Univ Fed Parana
dc.contributor.author.fl_str_mv Armani, Fernanda [UNIFESP]
Andersen, Monica L. [UNIFESP]
Andreatini, Roberto
Frussa-Filho, Roberto [UNIFESP]
Tufik, Sergio [UNIFESP]
Fernandes Galduroz, Jose Carlos [UNIFESP]
dc.subject.eng.fl_str_mv Adjunctive therapy
Lithium
Mania
Mice
Paradoxical sleep deprivation
Protein kinase C
Tamoxifen
topic Adjunctive therapy
Lithium
Mania
Mice
Paradoxical sleep deprivation
Protein kinase C
Tamoxifen
description Background: Previous studies have suggested that manic states and sleep deprivation could contribute to the pathophysiology of bipolar disorder (BD) through protein kinase C (PKC) signaling abnormalities. Moreover, adjunctive therapy has become a standard strategy in the management of BD patients who respond poorly to current pharmacological treatments. Aim: Thus, the aim of this study was to investigate the possible involvement of PKC inhibition by tamoxifen both separately or in combination with lithium, in paradoxical sleep deprivation (PSD)-induced hyperactivity, one facet of mania-like behavior. Materials & Methods: Adult male C57BL/6J mice were randomly distributed (n = 7/group) in 24-h PSD or control groups and injected intraperitoneally (i.p.) with vehicle, lithium (50, 100, or 150 mg/kg) or tamoxifen (0.5, 1.0, or 2.0 mg/kg experiment 1). in a second experiment, mice were injected i.p. with vehicle or a combination of subeffective doses of lithium and tamoxifen. Animals were subjected to a protocol based on repetitive PSD conditions, followed by assessment of locomotion activity in the open-field task. Results: PSD significantly increased locomotor activity in both experiments. These behavioral changes were prevented by a treatment with lithium or tamoxifen, or a combined treatment with both lithium and tamoxifen. Discussion: Therefore, our findings suggest that lithium and tamoxifen exert reversal effects against PSD-induced hyperactivity in mice. Conclusion: Furthermore, tamoxifen as an adjunct to lithium therapy provides support for an alternative treatment of individuals who either do not respond adequately or cannot tolerate the adverse effects associated with therapeutic doses of lithium.
publishDate 2012
dc.date.issued.fl_str_mv 2012-01-01
dc.date.accessioned.fl_str_mv 2016-01-24T14:17:36Z
dc.date.available.fl_str_mv 2016-01-24T14:17:36Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Cns Neuroscience & Therapeutics. Hoboken: Wiley-Blackwell, v. 18, n. 2, p. 119-125, 2012.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/34356
http://dx.doi.org/10.1111/j.1755-5949.2010.00224.x
dc.identifier.issn.none.fl_str_mv 1755-5930
dc.identifier.doi.none.fl_str_mv 10.1111/j.1755-5949.2010.00224.x
dc.identifier.wos.none.fl_str_mv WOS:000300001700004
identifier_str_mv Cns Neuroscience & Therapeutics. Hoboken: Wiley-Blackwell, v. 18, n. 2, p. 119-125, 2012.
1755-5930
10.1111/j.1755-5949.2010.00224.x
WOS:000300001700004
url http://repositorio.unifesp.br/handle/11600/34356
http://dx.doi.org/10.1111/j.1755-5949.2010.00224.x
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Cns Neuroscience & Therapeutics
dc.rights.driver.fl_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 119-125
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
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
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