Effects of N-acetylcysteine on amphetamine-induced sensitization in mice

Detalhes bibliográficos
Autor(a) principal: Herrmann, Ana Paula
Data de Publicação: 2018
Outros Autores: Caetano, Roberta Andrejew, Benvenutti, Radharani, Gama, Clarissa Severino, Elisabetsky, Elaine
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/182147
Resumo: N-acetylcysteine (NAC) is beneficial in psychiatric conditions, including schizophrenia. Patients with schizophrenia exhibit mesolimbic dopamine hyperfunction consequent to an endogenous sensitization process. This sensitization can be modeled in rodents by repeated exposure to psychostimulants, provoking an enduring amplified response at subsequent exposure. The aim of this study was to investigate the effects of NAC on amphetamine sensitization in mice. Methods: D-amphetamine was administered to C57BL/6 mice three times a week for 3 weeks; the dose was increased weekly from 1 to 3 mg/kg. NAC (60 mg/kg) or saline was administered intraperitoneally before saline or amphetamine during the second and third weeks. After a 4-week washout period, latent inhibition (LI) and the locomotor response to amphetamine 2 mg/kg were assessed. Results: Sensitization disrupted LI and amplified the locomotor response; NAC disrupted LI in control mice. In sensitized animals, NAC attenuated the enhanced locomotion but failed to prevent LI disruption. Conclusion: NAC warrants consideration as a candidate for early intervention in ultra-high risk subjects due to its safety profile and the relevance of its mechanism of action. Supplementing this proposition, we report that NAC attenuates sensitization-induced locomotor enhancement in mice. The finding that NAC disrupted LI incites a cautionary note and requires clarification.
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spelling Herrmann, Ana PaulaCaetano, Roberta AndrejewBenvenutti, RadharaniGama, Clarissa SeverinoElisabetsky, Elaine2018-09-18T02:30:24Z20181516-4446http://hdl.handle.net/10183/182147001073425N-acetylcysteine (NAC) is beneficial in psychiatric conditions, including schizophrenia. Patients with schizophrenia exhibit mesolimbic dopamine hyperfunction consequent to an endogenous sensitization process. This sensitization can be modeled in rodents by repeated exposure to psychostimulants, provoking an enduring amplified response at subsequent exposure. The aim of this study was to investigate the effects of NAC on amphetamine sensitization in mice. Methods: D-amphetamine was administered to C57BL/6 mice three times a week for 3 weeks; the dose was increased weekly from 1 to 3 mg/kg. NAC (60 mg/kg) or saline was administered intraperitoneally before saline or amphetamine during the second and third weeks. After a 4-week washout period, latent inhibition (LI) and the locomotor response to amphetamine 2 mg/kg were assessed. Results: Sensitization disrupted LI and amplified the locomotor response; NAC disrupted LI in control mice. In sensitized animals, NAC attenuated the enhanced locomotion but failed to prevent LI disruption. Conclusion: NAC warrants consideration as a candidate for early intervention in ultra-high risk subjects due to its safety profile and the relevance of its mechanism of action. Supplementing this proposition, we report that NAC attenuates sensitization-induced locomotor enhancement in mice. The finding that NAC disrupted LI incites a cautionary note and requires clarification.application/pdfengRevista brasileira de psiquiatria = Brazilian journal of psychiatry. São Paulo. Vol. 40, n. 2 (abr./jun. 2018), p. 169-173AcetilcisteínaAnfetaminaEsquizofreniaComportamento animalModelos animais de doençasEstimulantes do sistema nervoso centralCamundongosSchizophreniaAcetylcysteineAmphetamineEffects of N-acetylcysteine on amphetamine-induced sensitization in miceinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001073425.pdfTexto completo (inglês)application/pdf447185http://www.lume.ufrgs.br/bitstream/10183/182147/1/001073425.pdfcaa0faebe3c72bffeec7e9e37a9bd912MD51TEXT001073425.pdf.txt001073425.pdf.txtExtracted Texttext/plain24190http://www.lume.ufrgs.br/bitstream/10183/182147/2/001073425.pdf.txtb94f059e5ef3ceecb73cc291f7a70cd8MD52THUMBNAIL001073425.pdf.jpg001073425.pdf.jpgGenerated Thumbnailimage/jpeg1861http://www.lume.ufrgs.br/bitstream/10183/182147/3/001073425.pdf.jpgdffcc7a5e75869f0585c2ca8761936c0MD5310183/1821472023-09-02 03:34:48.880786oai:www.lume.ufrgs.br:10183/182147Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-09-02T06:34:48Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
title Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
spellingShingle Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
Herrmann, Ana Paula
Acetilcisteína
Anfetamina
Esquizofrenia
Comportamento animal
Modelos animais de doenças
Estimulantes do sistema nervoso central
Camundongos
Schizophrenia
Acetylcysteine
Amphetamine
title_short Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
title_full Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
title_fullStr Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
title_full_unstemmed Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
title_sort Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
author Herrmann, Ana Paula
author_facet Herrmann, Ana Paula
Caetano, Roberta Andrejew
Benvenutti, Radharani
Gama, Clarissa Severino
Elisabetsky, Elaine
author_role author
author2 Caetano, Roberta Andrejew
Benvenutti, Radharani
Gama, Clarissa Severino
Elisabetsky, Elaine
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Herrmann, Ana Paula
Caetano, Roberta Andrejew
Benvenutti, Radharani
Gama, Clarissa Severino
Elisabetsky, Elaine
dc.subject.por.fl_str_mv Acetilcisteína
Anfetamina
Esquizofrenia
Comportamento animal
Modelos animais de doenças
Estimulantes do sistema nervoso central
Camundongos
topic Acetilcisteína
Anfetamina
Esquizofrenia
Comportamento animal
Modelos animais de doenças
Estimulantes do sistema nervoso central
Camundongos
Schizophrenia
Acetylcysteine
Amphetamine
dc.subject.eng.fl_str_mv Schizophrenia
Acetylcysteine
Amphetamine
description N-acetylcysteine (NAC) is beneficial in psychiatric conditions, including schizophrenia. Patients with schizophrenia exhibit mesolimbic dopamine hyperfunction consequent to an endogenous sensitization process. This sensitization can be modeled in rodents by repeated exposure to psychostimulants, provoking an enduring amplified response at subsequent exposure. The aim of this study was to investigate the effects of NAC on amphetamine sensitization in mice. Methods: D-amphetamine was administered to C57BL/6 mice three times a week for 3 weeks; the dose was increased weekly from 1 to 3 mg/kg. NAC (60 mg/kg) or saline was administered intraperitoneally before saline or amphetamine during the second and third weeks. After a 4-week washout period, latent inhibition (LI) and the locomotor response to amphetamine 2 mg/kg were assessed. Results: Sensitization disrupted LI and amplified the locomotor response; NAC disrupted LI in control mice. In sensitized animals, NAC attenuated the enhanced locomotion but failed to prevent LI disruption. Conclusion: NAC warrants consideration as a candidate for early intervention in ultra-high risk subjects due to its safety profile and the relevance of its mechanism of action. Supplementing this proposition, we report that NAC attenuates sensitization-induced locomotor enhancement in mice. The finding that NAC disrupted LI incites a cautionary note and requires clarification.
publishDate 2018
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dc.relation.ispartof.pt_BR.fl_str_mv Revista brasileira de psiquiatria = Brazilian journal of psychiatry. São Paulo. Vol. 40, n. 2 (abr./jun. 2018), p. 169-173
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