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Authordc.contributor.authorAcuña Castillo, Claudio 
Authordc.contributor.authorScorza, Cecilia es_CL
Authordc.contributor.authorReyes Parada, Miguel es_CL
Authordc.contributor.authorCassels Niven, Brucees_CL
Authordc.contributor.authorHuidobro Toro, Juan Pablo es_CL
Admission datedc.date.accessioned2012-05-18T15:04:15Z
Available datedc.date.available2012-05-18T15:04:15Z
Publication datedc.date.issued2000-06-06
Cita de ítemdc.identifier.citationLife Sciences 67:3241–3247, 2000 .es_CL
Identifierdc.identifier.issn3241–3247
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119402
Abstractdc.description.abstractTo assess the pharmacodynamic profile of ALEPH-2, a phenylisopropylamine derivative with alleged anxiolytic and hallucinogenic properties, Xenopus laevis oocytes were microinjected with either of the rat cRNA for the 5-HT2A or the 5-HT2C receptor. Concentration-response curves were obtained following the exposure of the oocytes to varying concentrations of either ALEPH-2 or 5-hydroxytryptamine (5-HT) for 10 s. ALEPH-2 is a partial agonist on the 5-HT2A receptor with a similar potency to 5-HT. In contrast, ALEPH-2 is a full 5-HT2C receptor agonist and is about 15-fold less potent than 5-HT. Pre-application of 1 mM ritanserin antagonized the responses induced by 5-HT and ALEPH-2 to the same extent; however, the 5-HT2A receptor is more sensitive to ritanserin blockade than the 5-HT2C receptor.es_CL
Patrocinadordc.description.sponsorshipSupport by DICYT Grant 029901 RP to MRP, FONDAP grant 13980001 and MIFAB (Millenium Institute for Fundamental and Applied Biology, funded in part by Ministerio de Planificación y Cooperación, Chile) to JPHT and IASBB to BKC is also acknowledged.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherElsevier Science Inc.es_CL
Keywordsdc.subjectALEPH-2; 5-hydroxytryptaminees_CL
Títulodc.titleALEPH-2, a suspected anxiolytic and putative hallucinogenic phenylisopropylamine derivative, is a 5-HT2a and 5-HT2c receptor agonistes_CL
Document typedc.typeArtículo de revista


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