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Authordc.contributor.authorAraya, Aníbal
Authordc.contributor.authorGallegos, Scarlet
Authordc.contributor.authorViveros, Rodrigo
Authordc.contributor.authorSan Martín, Loreto
Authordc.contributor.authorMuñoz, Braulio
Authordc.contributor.authorHarvey, Robert
Authordc.contributor.authorZeilhofer, Hanns U.
Authordc.contributor.authorAguallo, Luis G.
Admission datedc.date.accessioned2023-01-17T21:22:41Z
Available datedc.date.available2023-01-17T21:22:41Z
Publication datedc.date.issued2021
Cita de ítemdc.identifier.citationBr J Pharmacol. 2021;178:4691–4707.es_ES
Identifierdc.identifier.other10.1111/bph.15649
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/191589
Abstractdc.description.abstractBackground and Purpose: Glycine receptors composed of α1 and β subunits are primarily found in the spinal cord and brainstem and are potentiated by ethanol (10–100 mM). However, much less is known about the presence, composition and ethanol sensitivity of these receptors in higher CNS regions. Here, we examined two regions of the brain reward system, the ventral tegmental area (VTA) and the prefrontal cortex (PFC), to determine their glycine receptor subunit composition and sensitivity to ethanol. Experimental Approach: We used Western blot, immunohistochemistry and electrophysiological techniques in three different models: wild-type C57BL/6, glycine receptor subunit α1 knock-in and glycine receptor subunit α2 knockout mice. Key Results: Similar levels of α and β receptor subunits were detected in both brain regions, and electrophysiological recordings demonstrated the presence of glycineactivated currents in both areas. Sensitivity of glycine receptors to glycine was lower in the PFC compared with VTA. Picrotoxin only partly blocked the glycine-activated current in the PFC and VTA, indicating that both regions express heteromeric αβ receptors. Glycine receptors in VTA neurons, but not in PFC neurons, were potentiated by ethanol. Conclusion and Implications: Glycine receptors in VTA neurons from WT and α2 KO mice were potentiated by ethanol, but not in neurons from the α1 KI mice, supporting the conclusion that α1 glycine receptors are predominantly expressed in the VTA. By contrast, glycine receptors in PFC neurons were not potentiated in any of the mouse models studied, suggesting the presence of α2/α3/α4, rather than α1 glycine receptor subunits.es_ES
Patrocinadordc.description.sponsorshipUK Research & Innovation (UKRI) Medical Research Council UK (MRC) G0500833 Fondo de Fomento al Desarrollo Cientifico y Tecnologico DPI 20140008 United States Department of Health & Human Services National Institutes of Health (NIH) - USA NIH National Institute on Alcohol Abuse & Alcoholism (NIAAA) RO1 AA 025718 Aparece en contenido como:National Institute on Alcohol Abuse and Alcoholismes_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherWileyes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceBritish Journal of Pharmacologyes_ES
Keywordsdc.subjectEthanoles_ES
Keywordsdc.subjectGlycine receptorses_ES
Keywordsdc.subjectPFCes_ES
Keywordsdc.subjectReward systemes_ES
Keywordsdc.subjectSubunit compositiones_ES
Keywordsdc.subjectVTAes_ES
Títulodc.titlePresence of ethanol-sensitive and ethanol-insensitive glycine receptors in the ventral tegmental area and prefrontal cortex in micees_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorcfres_ES
Indexationuchile.indexArtículo de publícación WoSes_ES


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States