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Publicação:
Effects of N-acetylcysteine treatment on ethanol's rewarding properties and dopaminergic alterations in mesocorticolimbic and nigrostriatal pathways

dc.contributor.authorLaverde, Celina Ferrari [UNESP]
dc.contributor.authorMorais-Silva, Gessynger [UNESP]
dc.contributor.authorAmaral, Vanessa Cristiane Santana [UNESP]
dc.contributor.authorMarin, Marcelo Tadeu [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionExact and Technological Sciences Campus
dc.date.accessioned2021-06-25T10:56:05Z
dc.date.available2021-06-25T10:56:05Z
dc.date.issued2021-01-01
dc.description.abstractRecent reports have shown that N-acetylcysteine (N-AC) has beneficial effects in the treatment of cocaine and nicotine abuse. Considering the similar neurobiologic mechanisms involved in the development of addiction to different drugs, N-AC treatment could be useful in the treatment of ethanol abuse. The rewarding properties of the drugs of abuse plays an important role in the development of addiction and can be studied using the conditioned place preference (CPP) paradigm. Thus, to study the effects of N-AC treatment in the rewarding effects of ethanol, we investigated the effects of N-AC administration in the ethanol-induced CPP and neurochemical alterations within the mesocorticolimbic and the nigrostriatal dopaminergic pathways. Adult male Swiss mice were pretreated with N-AC (60 or 120 mg/kg intraperitoneal) and tested for the development, expression, or extinction of the ethanol-induced CPP. Another cohort of animals received N-AC (60 or 120 mg/kg intraperitoneal) 2-h before an acute administration of ethanol and had their brains removed for dopamine and its metabolites quantification in the mesocorticolimbic and nigrostriatal pathways. Pretreatment with N-AC (120 mg/kg) blocked the development of ethanol-induced CPP. On the other hand, N-AC at both doses did not alter the expression nor the extinction of ethanol-induced CPP. N-AC increased 3,4-dihydroxyphenylacetic acid content in the medial prefrontal cortex and dopaminergic turnover within the substantia nigra. Besides that, there was an increase in dopamine content in the nucleus accumbens of ethanol-treated animals. In summary, N-AC treatment blocked the development of ethanol CPP, without altering ethanol effects on dopaminergic neurotransmission.en
dc.description.affiliationDepartment of Drugs and Medicines São Paulo State University (UNESP) School of Pharmaceutical Sciences of Araraquara Laboratory of Pharmacology
dc.description.affiliationJoint Graduate Program in Physiological Sciences (PIPGCF) UFSCar/UNESP
dc.description.affiliationLaboratory of Pharmacology and Toxicology of Natural and Synthetic Products State University of Goias Exact and Technological Sciences Campus
dc.description.affiliationUnespDepartment of Drugs and Medicines São Paulo State University (UNESP) School of Pharmaceutical Sciences of Araraquara Laboratory of Pharmacology
dc.description.affiliationUnespJoint Graduate Program in Physiological Sciences (PIPGCF) UFSCar/UNESP
dc.format.extent239-250
dc.identifierhttp://dx.doi.org/10.1097/FBP.0000000000000613
dc.identifier.citationBehavioural Pharmacology, p. 239-250.
dc.identifier.doi10.1097/FBP.0000000000000613
dc.identifier.issn1473-5849
dc.identifier.issn0955-8810
dc.identifier.scopus2-s2.0-85102965273
dc.identifier.urihttp://hdl.handle.net/11449/207492
dc.language.isoeng
dc.relation.ispartofBehavioural Pharmacology
dc.sourceScopus
dc.subjectaddiction
dc.subjectconditioned place preference
dc.subjectcystine-glutamate antiporter
dc.subjectdopamine
dc.subjectethanol
dc.subjectN-acetylcysteine
dc.subjectrat
dc.titleEffects of N-acetylcysteine treatment on ethanol's rewarding properties and dopaminergic alterations in mesocorticolimbic and nigrostriatal pathwaysen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.departmentFármacos e Medicamentos - FCFpt

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