The impact of cocaine on adult hippocampal neurogenesis: Potential neurobiological mechanisms and contributions to maladaptive cognition in cocaine addiction disorder

dc.centroFacultad de Psicología y Logopediaes_ES
dc.contributor.authorCastilla-Ortega, María Estela
dc.contributor.authorLadrón de Guevara-Miranda, David
dc.contributor.authorSerrano, Antonia
dc.contributor.authorPavón, Francisco Javier
dc.contributor.authorSuárez, Juan
dc.contributor.authorRodriguez-de-Fonseca, Fernando
dc.contributor.authorSantín-Núñez, Luis Javier
dc.date.accessioned2024-09-30T17:46:34Z
dc.date.available2024-09-30T17:46:34Z
dc.date.created2024-09-24
dc.date.issued2017-10-01
dc.departamentoPsicobiología y Metodología de las Ciencias del Comportamiento
dc.description.abstractAfter discovering that addictive drugs alter adult neurogenesis, the potential role of adult-born hippocampal neurons in drug addiction has become a promising research field, in which cocaine is the most frequently investigated drug. Although a substantial amount of pre-clinical evidence has accumulated, additional studies are required to reveal the mechanisms by which cocaine modulates adult hippocampal neurogenesis (AHN) and determine whether these adult-born neurons have a role in cocaine-related behaviors, such as cocaine-mediated cognitive symptoms. First, this review will summarize the cocaine-induced alterations in a number of neurobiological factors (neurotransmitters, neurotrophins, glucocorticoids, inflammatory mediators) that likely regulate both hippocampal-dependent learning and adult hippocampal neurogenesis after cocaine exposure. A separate section will provide a detailed review of the available literature that challenges the common view that cocaine reduces adult hippocampal neurogenesis. In fact, cocaine has a short-term anti-proliferative role, but the young adult-born neurons are apparently spared, or even enhanced, following certain cocaine protocols. Thus, we will try to reconcile this evidence with the hippocampal-dependent cognitive symptoms that are typically observed in cocaine addicts, and we will propose new directions for future studies to test the relevant hypothesis. Based on the evidence presented here, the regulation of adult hippocampal neurogenesis might be one of the many mechanisms by which cocaine sculpts hippocampus-dependent learning.es_ES
dc.description.sponsorshipMinisterio de Economía y Competitividad (Agencia Estatal de Investigación) & Fondo Europeo de Desarrollo Regional (AEI/FEDER, UE) (PSI2015-73156-JIN, PSI2013-44901-P); Red de Trastornos Adictivos (RD16/0017/0001); Ministerio de Educación, Cultura y Deporte (FPU13/04819); Sistema Nacional de Salud-Instituto de Salud Carlos III (CP14/00173, CP12/03109 y CP14/00212).es_ES
dc.identifier.citationCastilla-Ortega, E., Ladrón de Guevara-Miranda, D., Serrano, A., Pavón, F. J., Suárez, J., Rodríguez de Fonseca, F., & Santín, L. J. (2017). The impact of cocaine on adult hippocampal neurogenesis: Potential neurobiological mechanisms and contributions to maladaptive cognition in cocaine addiction disorder. Biochemical pharmacology, 141, 100–117. https://doi.org/10.1016/j.bcp.2017.05.003es_ES
dc.identifier.doi10.1016/j.bcp.2017.05.003
dc.identifier.urihttps://hdl.handle.net/10630/34087
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCocaínaes_ES
dc.subject.otherVulnerabilityes_ES
dc.subject.otherAssociative memoryes_ES
dc.subject.otherConditioned place preferencees_ES
dc.subject.otherWithdrawales_ES
dc.subject.otherRelapsees_ES
dc.titleThe impact of cocaine on adult hippocampal neurogenesis: Potential neurobiological mechanisms and contributions to maladaptive cognition in cocaine addiction disorderes_ES
dc.typejournal articlees_ES
dc.type.hasVersionAMes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationdf54f7b6-6c40-45f9-b840-3a38e3501fe9
relation.isAuthorOfPublication8863466f-3de6-430a-b11d-8657a4bfedd4
relation.isAuthorOfPublication.latestForDiscoverydf54f7b6-6c40-45f9-b840-3a38e3501fe9

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