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Sex-dependent influence of chronic mild stress (CMS) on voluntary alcohol consumption; study of neurobiological consequences

dc.contributor.authorMarco López, Eva M.
dc.contributor.authorBallesta, Javier Antonio
dc.contributor.authorIrala, Carlos
dc.contributor.authorHernández, María Donina
dc.contributor.authorSerrano, María Elisa
dc.contributor.authorMela Rivas, Virginia
dc.contributor.authorLópezGallardo, Meritxell
dc.contributor.authorViveros, María Paz
dc.date.accessioned2023-06-17T22:04:57Z
dc.date.available2023-06-17T22:04:57Z
dc.date.issued2017-01
dc.description.abstractAlcohol use disorder and depression are highly comorbid, and both conditions exhibit important sexual dimorphisms. Here, we aimed to investigate voluntary alcohol consumption after 6 weeks of chronic mild stress (CMS) in Wistar rats – employed as an animal model of depression. Male and female rats were investigated, and changes in several molecular markers were analysed in frontal cortex (FCx) and hippocampal formation (HF). CMS induced depressive-like responses in the forced swimming test - increased immobility time - in male and female animals, without affecting anhedonia (sucrose preference test) nor motor activity (holeboard); body weight gain and food intake were diminished only among CMS males. Voluntary alcohol consumption was evaluated in a two-bottle choice paradigm (ethanol 20% versus tap water) for 4 consecutive days; females exhibited a higher preference for alcohol compared to male animals. In particular, alcohol consumption was significantly higher among CMS females compared to CMS male animals. Remarkably, similar changes in both male and female animals exposed to CMS were observed regarding the expression levels of NCAM-140 KDa (decrease), GFAP and CB1R expression (increase) within the FCx as well as for HF PSD-95 levels (increase). However, contrasting effects in males and females were reported in relation to synaptophysin (SYN) protein levels within the FCx, HF CB1R expression (a decrease among male animals but an increase in females); while the opposite pattern was observed for NCAM-140 KDa protein levels in the HF. A decrease in CB2R expression was only observed in the HF of CMS-females. The present study suggests that male and female animals might be differentially affected by CMS regarding later voluntary alcohol consumption. In this initial approach, cortical SYN, and NCAM-140 KDa, CB1R and CB2R expression within the HF have arisen as potential candidates to explain such sex differences in behaviour. However, the depression-alcoholism relationship still deserves further investigation.
dc.description.departmentDepto. de Genética, Fisiología y Microbiología
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.sponsorshipUCM-BSCH
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/44407
dc.identifier.doi10.1016/j.pbb.2016.11.005
dc.identifier.issn0091-3057
dc.identifier.officialurlhttp://www.sciencedirect.com/science/journal/00913057?sdc=1
dc.identifier.urihttps://hdl.handle.net/20.500.14352/18032
dc.journal.titlePharmacology Biochemistry and Behavior
dc.language.isoeng
dc.page.final80
dc.page.initial68
dc.publisherElsevier
dc.relation.projectIDRETICS (RD2012/0028/0021)
dc.relation.projectIDUCM (951579)
dc.rights.accessRightsrestricted access
dc.subject.cdu591.1
dc.subject.cdu612.82
dc.subject.keywordAlcohol Depression
dc.subject.keywordAnimal models
dc.subject.keywordSex differences
dc.subject.keywordTwo-bottle choice
dc.subject.keywordCannabinoid receptors
dc.subject.keywordGFAP
dc.subject.keywordSynaptic plasticity
dc.subject.keywordFrontal cortex
dc.subject.keywordHippocampus
dc.subject.ucmFisiología animal (Biología)
dc.subject.ucmNeurociencias (Biológicas)
dc.subject.unesco2401.13 Fisiología Animal
dc.subject.unesco2490 Neurociencias
dc.titleSex-dependent influence of chronic mild stress (CMS) on voluntary alcohol consumption; study of neurobiological consequences
dc.typejournal article
dc.volume.number152
dspace.entity.typePublication
relation.isAuthorOfPublicationba7d275d-44e1-46a8-b304-d1dcf3a3cc64
relation.isAuthorOfPublication.latestForDiscoveryba7d275d-44e1-46a8-b304-d1dcf3a3cc64

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