Please use this identifier to cite or link to this item: https://doi.org/10.1038/tp.2017.34
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dc.titleEffects of naltrexone are influenced by childhood adversity during negative emotional processing in addiction recovery
dc.contributor.authorSavulich, G
dc.contributor.authorRiccelli, R
dc.contributor.authorPassamonti, L
dc.contributor.authorCorreia, M
dc.contributor.authorDeakin, J.F.W
dc.contributor.authorElliott, R
dc.contributor.authorFlechais, R.S.A
dc.contributor.authorLingford-Hughes, A.R
dc.contributor.authorMcGonigle, J
dc.contributor.authorMurphy, A
dc.contributor.authorNutt, D.J
dc.contributor.authorOrban, C
dc.contributor.authorPaterson, L.M
dc.contributor.authorReed, L.J
dc.contributor.authorSmith, D.G
dc.contributor.authorSuckling, J
dc.contributor.authorTait, R
dc.contributor.authorTaylor, E.M
dc.contributor.authorSahakian, B.J
dc.contributor.authorRobbins, T.W
dc.contributor.authorErsche, K.D
dc.date.accessioned2020-11-17T06:34:42Z
dc.date.available2020-11-17T06:34:42Z
dc.date.issued2017
dc.identifier.citationSavulich, G, Riccelli, R, Passamonti, L, Correia, M, Deakin, J.F.W, Elliott, R, Flechais, R.S.A, Lingford-Hughes, A.R, McGonigle, J, Murphy, A, Nutt, D.J, Orban, C, Paterson, L.M, Reed, L.J, Smith, D.G, Suckling, J, Tait, R, Taylor, E.M, Sahakian, B.J, Robbins, T.W, Ersche, K.D (2017). Effects of naltrexone are influenced by childhood adversity during negative emotional processing in addiction recovery. Translational Psychiatry 7 (3) : e1054. ScholarBank@NUS Repository. https://doi.org/10.1038/tp.2017.34
dc.identifier.issn2158-3188
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/183541
dc.description.abstractNaltrexone is an opioid receptor antagonist used in the management of alcohol dependence. Although the endogenous opioid system has been implicated in emotion regulation, the effects of mu-opioid receptor blockade on brain systems underlying negative emotional processing are not clear in addiction. Individuals meeting criteria for alcohol dependence alone (n=18, alcohol) and in combination with cocaine and/or opioid dependence (n=21, alcohol/drugs) and healthy individuals without a history of alcohol or drug dependence (n=21) were recruited. Participants were alcohol and drug abstinent before entered into this double-blind, placebo-controlled, randomized, crossover study. Functional magnetic resonance imaging was used to investigate brain response while viewing aversive and neutral images relative to baseline on 50 mg of naltrexone and placebo. We found that naltrexone modulated task-related activation in the medial prefrontal cortex and functional connectivity between the anterior cingulate cortex and the hippocampus as a function of childhood adversity (for aversive versus neutral images) in all groups. Furthermore, there was a group-by-treatment-by-condition interaction in the right amygdala, which was mainly driven by a normalization of response for aversive relative to neutral images under naltrexone in the alcohol/drugs group. We conclude that early childhood adversity is one environmental factor that influences pharmacological response to naltrexone. Pharmacotherapy with naltrexone may also have some ameliorative effects on negative emotional processing in combined alcohol and drug dependence, possibly due to alterations in endogenous opioid transmission or the kappa-opioid receptor antagonist actions of naltrexone. © 2017 The Author(s).
dc.publisherSpringer Nature
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectnaltrexone
dc.subjectplacebo
dc.subjectnaltrexone
dc.subjectnarcotic antagonist
dc.subjectadult
dc.subjectalcoholism
dc.subjectanterior cingulate
dc.subjectArticle
dc.subjectaversive behavior
dc.subjectcontrolled study
dc.subjectcrossover procedure
dc.subjectdouble blind procedure
dc.subjectdrug dependence
dc.subjectemotion
dc.subjectenvironmental factor
dc.subjectfemale
dc.subjectfunctional connectivity
dc.subjectfunctional magnetic resonance imaging
dc.subjecthippocampus
dc.subjecthuman
dc.subjectmale
dc.subjectmedial prefrontal cortex
dc.subjectrandomized controlled trial
dc.subjectalcoholism
dc.subjectamygdala
dc.subjectassociation
dc.subjectbrain
dc.subjectcase control study
dc.subjectchildhood trauma survivor
dc.subjectcingulate gyrus
dc.subjectcocaine dependence
dc.subjectdiagnostic imaging
dc.subjectdrug dependence
dc.subjectdrug effects
dc.subjectfunctional neuroimaging
dc.subjectmiddle aged
dc.subjectnerve tract
dc.subjectnuclear magnetic resonance imaging
dc.subjectopiate addiction
dc.subjectpathophysiology
dc.subjectprefrontal cortex
dc.subjectyoung adult
dc.subjectAdult
dc.subjectAdult Survivors of Child Adverse Events
dc.subjectAlcoholism
dc.subjectAmygdala
dc.subjectBrain
dc.subjectCase-Control Studies
dc.subjectCocaine-Related Disorders
dc.subjectCross-Over Studies
dc.subjectCues
dc.subjectDouble-Blind Method
dc.subjectFemale
dc.subjectFunctional Neuroimaging
dc.subjectGyrus Cinguli
dc.subjectHippocampus
dc.subjectHumans
dc.subjectMagnetic Resonance Imaging
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNaltrexone
dc.subjectNarcotic Antagonists
dc.subjectNeural Pathways
dc.subjectOpioid-Related Disorders
dc.subjectPrefrontal Cortex
dc.subjectSubstance-Related Disorders
dc.subjectYoung Adult
dc.typeArticle
dc.contributor.departmentELECTRICAL AND COMPUTER ENGINEERING
dc.description.doi10.1038/tp.2017.34
dc.description.sourcetitleTranslational Psychiatry
dc.description.volume7
dc.description.issue3
dc.description.pagee1054
dc.published.statePublished
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