Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice

Detalhes bibliográficos
Autor(a) principal: Fallopa, Paula [UNIFESP]
Data de Publicação: 2012
Outros Autores: Escosteguy-Neto, João Carlos [UNIFESP], Varela, Patricia [UNIFESP], Carvalho, Thiago Nogueira [UNIFESP], Tabosa, Angela Maria Florencio [UNIFESP], Santos-Junior, Jair Guilherme [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/35191
http://dx.doi.org/10.1017/S1461145711001325
Resumo: Extracellular signal-regulated kinase (ERK) plays a role in neuronal changes induced by repeated drug exposure. Given that electroacupuncture reverses locomotor sensitization induced by ethanol, we investigated whether this effect is parallel to ERK signalling. Mice received daily ethanol (2 g/kg i.p), for 21 d. Electroacupuncture was performed daily, during four (subsequent) days of ethanol withdrawal. the stimulus of 2 Hz or 100 Hz was provided in combinations of two acupoints: Ea1 (ST-36/Zusanli and PC-6/Neiguan) or Ea2 (Du-14/Dazhui and Du-20/Baihui). the specificity of acupoint effects were assessed by the inclusion of additional groups: Ea3 (ST-25/Tianshu - acupoint used for other non-related disorders), Sham1 or Sham2 (transdermic stimulation near the respective acupoints). the control group was only handled during withdrawal and the saline group was chronically treated with saline and handled similarly to controls. At day 5 of withdrawal, each group was divided in two subgroups, according to the presence or absence of ethanol challenge. the animals were perfused and their brains processed for pERK immunohistochemistry. Only Ea1 at 100 Hz (Ea1_100) and Ea2 at 2 Hz (Ea2_2) reversed locomotor sensitization induced by ethanol. Ethanol withdrawal decreases pERK in the dorsomedial striatum. This decrease is not abolished by electroacupuncture. Conversely, ethanol challenge increases pERK in the dorsomedial striatum, infralimbic cortex and central nucleus of amygdala. the specificity of acupoint stimulation to reverse these increases was seen only for Ea2_2, in the infralimbic cortex and dorsomedial striatum. Therefore, behavioural effects of Ea2_2 (but not Ea1_100) depend, at least in part, on ERK signalling.
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spelling Fallopa, Paula [UNIFESP]Escosteguy-Neto, João Carlos [UNIFESP]Varela, Patricia [UNIFESP]Carvalho, Thiago Nogueira [UNIFESP]Tabosa, Angela Maria Florencio [UNIFESP]Santos-Junior, Jair Guilherme [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Fac Med Sci2016-01-24T14:27:35Z2016-01-24T14:27:35Z2012-09-01International Journal of Neuropsychopharmacology. New York: Cambridge Univ Press, v. 15, n. 8, p. 1121-1133, 2012.1461-1457http://repositorio.unifesp.br/handle/11600/35191http://dx.doi.org/10.1017/S146114571100132510.1017/S1461145711001325WOS:000307188000010Extracellular signal-regulated kinase (ERK) plays a role in neuronal changes induced by repeated drug exposure. Given that electroacupuncture reverses locomotor sensitization induced by ethanol, we investigated whether this effect is parallel to ERK signalling. Mice received daily ethanol (2 g/kg i.p), for 21 d. Electroacupuncture was performed daily, during four (subsequent) days of ethanol withdrawal. the stimulus of 2 Hz or 100 Hz was provided in combinations of two acupoints: Ea1 (ST-36/Zusanli and PC-6/Neiguan) or Ea2 (Du-14/Dazhui and Du-20/Baihui). the specificity of acupoint effects were assessed by the inclusion of additional groups: Ea3 (ST-25/Tianshu - acupoint used for other non-related disorders), Sham1 or Sham2 (transdermic stimulation near the respective acupoints). the control group was only handled during withdrawal and the saline group was chronically treated with saline and handled similarly to controls. At day 5 of withdrawal, each group was divided in two subgroups, according to the presence or absence of ethanol challenge. the animals were perfused and their brains processed for pERK immunohistochemistry. Only Ea1 at 100 Hz (Ea1_100) and Ea2 at 2 Hz (Ea2_2) reversed locomotor sensitization induced by ethanol. Ethanol withdrawal decreases pERK in the dorsomedial striatum. This decrease is not abolished by electroacupuncture. Conversely, ethanol challenge increases pERK in the dorsomedial striatum, infralimbic cortex and central nucleus of amygdala. the specificity of acupoint stimulation to reverse these increases was seen only for Ea2_2, in the infralimbic cortex and dorsomedial striatum. Therefore, behavioural effects of Ea2_2 (but not Ea1_100) depend, at least in part, on ERK signalling.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Universidade Federal de São Paulo, Neurobiol Lab, Grp Neuronal Plast & Psychiat Disorders, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Orthoped & Traumatol, Div Chinese Med Acupuncture, São Paulo, BrazilFac Med Sci, Dept Physiol Sci, São Paulo, BrazilUniversidade Federal de São Paulo, Neurobiol Lab, Grp Neuronal Plast & Psychiat Disorders, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Orthoped & Traumatol, Div Chinese Med Acupuncture, São Paulo, BrazilFAPESP: 2010-03896-7FAPESP: 2007/55458-0Web of Science1121-1133engCambridge Univ PressInternational Journal of Neuropsychopharmacologyhttp://journals.cambridge.org/action/displaySpecialPage?pageId=4676info:eu-repo/semantics/openAccessAlcoholelectroacupuncturelocomotor sensitizationpERKElectroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in miceinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlereponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/351912022-07-08 10:28:59.2metadata only accessoai:repositorio.unifesp.br:11600/35191Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652022-07-08T13:28:59Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice
title Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice
spellingShingle Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice
Fallopa, Paula [UNIFESP]
Alcohol
electroacupuncture
locomotor sensitization
pERK
title_short Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice
title_full Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice
title_fullStr Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice
title_full_unstemmed Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice
title_sort Electroacupuncture reverses ethanol-induced locomotor sensitization and subsequent pERK expression in mice
author Fallopa, Paula [UNIFESP]
author_facet Fallopa, Paula [UNIFESP]
Escosteguy-Neto, João Carlos [UNIFESP]
Varela, Patricia [UNIFESP]
Carvalho, Thiago Nogueira [UNIFESP]
Tabosa, Angela Maria Florencio [UNIFESP]
Santos-Junior, Jair Guilherme [UNIFESP]
author_role author
author2 Escosteguy-Neto, João Carlos [UNIFESP]
Varela, Patricia [UNIFESP]
Carvalho, Thiago Nogueira [UNIFESP]
Tabosa, Angela Maria Florencio [UNIFESP]
Santos-Junior, Jair Guilherme [UNIFESP]
author2_role author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Fac Med Sci
dc.contributor.author.fl_str_mv Fallopa, Paula [UNIFESP]
Escosteguy-Neto, João Carlos [UNIFESP]
Varela, Patricia [UNIFESP]
Carvalho, Thiago Nogueira [UNIFESP]
Tabosa, Angela Maria Florencio [UNIFESP]
Santos-Junior, Jair Guilherme [UNIFESP]
dc.subject.eng.fl_str_mv Alcohol
electroacupuncture
locomotor sensitization
pERK
topic Alcohol
electroacupuncture
locomotor sensitization
pERK
description Extracellular signal-regulated kinase (ERK) plays a role in neuronal changes induced by repeated drug exposure. Given that electroacupuncture reverses locomotor sensitization induced by ethanol, we investigated whether this effect is parallel to ERK signalling. Mice received daily ethanol (2 g/kg i.p), for 21 d. Electroacupuncture was performed daily, during four (subsequent) days of ethanol withdrawal. the stimulus of 2 Hz or 100 Hz was provided in combinations of two acupoints: Ea1 (ST-36/Zusanli and PC-6/Neiguan) or Ea2 (Du-14/Dazhui and Du-20/Baihui). the specificity of acupoint effects were assessed by the inclusion of additional groups: Ea3 (ST-25/Tianshu - acupoint used for other non-related disorders), Sham1 or Sham2 (transdermic stimulation near the respective acupoints). the control group was only handled during withdrawal and the saline group was chronically treated with saline and handled similarly to controls. At day 5 of withdrawal, each group was divided in two subgroups, according to the presence or absence of ethanol challenge. the animals were perfused and their brains processed for pERK immunohistochemistry. Only Ea1 at 100 Hz (Ea1_100) and Ea2 at 2 Hz (Ea2_2) reversed locomotor sensitization induced by ethanol. Ethanol withdrawal decreases pERK in the dorsomedial striatum. This decrease is not abolished by electroacupuncture. Conversely, ethanol challenge increases pERK in the dorsomedial striatum, infralimbic cortex and central nucleus of amygdala. the specificity of acupoint stimulation to reverse these increases was seen only for Ea2_2, in the infralimbic cortex and dorsomedial striatum. Therefore, behavioural effects of Ea2_2 (but not Ea1_100) depend, at least in part, on ERK signalling.
publishDate 2012
dc.date.issued.fl_str_mv 2012-09-01
dc.date.accessioned.fl_str_mv 2016-01-24T14:27:35Z
dc.date.available.fl_str_mv 2016-01-24T14:27:35Z
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 International Journal of Neuropsychopharmacology. New York: Cambridge Univ Press, v. 15, n. 8, p. 1121-1133, 2012.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/35191
http://dx.doi.org/10.1017/S1461145711001325
dc.identifier.issn.none.fl_str_mv 1461-1457
dc.identifier.doi.none.fl_str_mv 10.1017/S1461145711001325
dc.identifier.wos.none.fl_str_mv WOS:000307188000010
identifier_str_mv International Journal of Neuropsychopharmacology. New York: Cambridge Univ Press, v. 15, n. 8, p. 1121-1133, 2012.
1461-1457
10.1017/S1461145711001325
WOS:000307188000010
url http://repositorio.unifesp.br/handle/11600/35191
http://dx.doi.org/10.1017/S1461145711001325
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv International Journal of Neuropsychopharmacology
dc.rights.driver.fl_str_mv http://journals.cambridge.org/action/displaySpecialPage?pageId=4676
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://journals.cambridge.org/action/displaySpecialPage?pageId=4676
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1121-1133
dc.publisher.none.fl_str_mv Cambridge Univ Press
publisher.none.fl_str_mv Cambridge Univ Press
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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