Effects of N-acetylcysteine on amphetamine-induced sensitization in mice
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , |
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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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 |
dc.date.accessioned.fl_str_mv |
2018-09-18T02:30:24Z |
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2018 |
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http://hdl.handle.net/10183/182147 |
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eng |
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eng |
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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