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Plasma concentrations of oleoylethanolamide and other acylethanolamides are altered in alcohol-dependent patients: effect of length of abstinence

dc.contributor.authorGarcía Marchena, Nuria
dc.contributor.authorPavón Carrasco, Francisco Javier
dc.contributor.authorPastor, A
dc.contributor.authorAraos, P
dc.contributor.authorPedraz, M
dc.contributor.authorRomero Sanchiz, P
dc.contributor.authorCalado, M
dc.contributor.authorSuárez, J
dc.contributor.authorCastilla Ortega, E
dc.contributor.authorOrio Ortiz, Laura
dc.contributor.authorBoronat, A
dc.contributor.authorTorrens, M
dc.contributor.authorRubio Valladolid, Gabriel
dc.contributor.authorRubio, G
dc.contributor.authorde la Torre, Rafael
dc.contributor.authorRodríguez De Fonseca, Fernando Antonio
dc.contributor.authorSerrano, A
dc.date.accessioned2024-02-02T10:01:03Z
dc.date.available2024-02-02T10:01:03Z
dc.date.issued2016-02-25
dc.description.abstractAcylethanolamides are a family of endogenous lipid mediators that are involved in physiological and behavioral processes associated with addiction. Recently, oleoylethanolamide (OEA) has been reported to reduce alcohol intake and relapse in rodents but the contribution of OEA and other acylethanolamides in alcohol addiction in humans is unknown. The present study is aimed to characterize the plasma acylethanolamides in alcohol dependence. Seventy-nine abstinent alcohol-dependent subjects (27 women) recruited from outpatient treatment programs and age-/sex-/body mass-matched healthy volunteers (28 women) were clinically assessed with the diagnostic interview PRISM according to the DSM-IV-TR after blood extraction for quantification of acylethanolamide concentrations in the plasma. Our results indicate that all acylethanolamides were significantly increased in alcohol-dependent patients compared with control subjects (p < 0.001). A logistic model based on these acylethanolamides was developed to distinguish alcohol-dependent patients from controls and included OEA, arachidonoylethanolamide (AEA) and docosatetraenoylethanolamide (DEA), providing a high discriminatory power according to area under the curve [AUC = 0.92 (95%CI: 0.87–0.96), p < 0.001]. Additionally, we found a significant effect of the duration of alcohol abstinence on the concentrations of OEA, AEA and DEA using a regression model (p < 0.05, p < 0.01 and p < 0.001, respectively), which was confirmed by a negative correlation (rho = −0.31, −0.40 and −0.44, respectively). However, acylethanolamides were not influenced by the addiction alcohol severity, duration of problematic alcohol use or diagnosis of psychiatric comorbidity. Our results support the preclinical studies and suggest that OEA, AEA and DEA are altered in alcohol-dependence during abstinence and that might act as potential markers for predicting length of alcohol abstinence.
dc.description.departmentDepto. de Psicobiología y Metodología en Ciencias del Comportamiento
dc.description.facultyFac. de Psicología
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.doi10.1111/adb.12408
dc.identifier.essn1369-1600
dc.identifier.issn1355-6215
dc.identifier.officialurlhttps://onlinelibrary.wiley.com/doi/10.1111/adb.12408
dc.identifier.urihttps://hdl.handle.net/20.500.14352/98143
dc.issue.number5
dc.journal.titleAddiction Biology
dc.language.isoeng
dc.page.final1377
dc.page.initial1366
dc.publisherWiley
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.keywordAbstinence
dc.subject.keywordAcylethanolamides
dc.subject.keywordAlcohol use disorder
dc.subject.keywordDSM-IV-TR
dc.subject.keywordOleoylethanolamide
dc.subject.keywordPsychiatric comorbidity
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco32 Ciencias Médicas
dc.titlePlasma concentrations of oleoylethanolamide and other acylethanolamides are altered in alcohol-dependent patients: effect of length of abstinence
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number22
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery8831c820-c977-43a1-b230-c1f73b8ed0f5

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