Please use this identifier to cite or link to this item: https://doi.org/10.1038/tp.2017.34
Title: Effects of naltrexone are influenced by childhood adversity during negative emotional processing in addiction recovery
Authors: Savulich, 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
Keywords: naltrexone
placebo
naltrexone
narcotic antagonist
adult
alcoholism
anterior cingulate
Article
aversive behavior
controlled study
crossover procedure
double blind procedure
drug dependence
emotion
environmental factor
female
functional connectivity
functional magnetic resonance imaging
hippocampus
human
male
medial prefrontal cortex
randomized controlled trial
alcoholism
amygdala
association
brain
case control study
childhood trauma survivor
cingulate gyrus
cocaine dependence
diagnostic imaging
drug dependence
drug effects
functional neuroimaging
middle aged
nerve tract
nuclear magnetic resonance imaging
opiate addiction
pathophysiology
prefrontal cortex
young adult
Adult
Adult Survivors of Child Adverse Events
Alcoholism
Amygdala
Brain
Case-Control Studies
Cocaine-Related Disorders
Cross-Over Studies
Cues
Double-Blind Method
Female
Functional Neuroimaging
Gyrus Cinguli
Hippocampus
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Naltrexone
Narcotic Antagonists
Neural Pathways
Opioid-Related Disorders
Prefrontal Cortex
Substance-Related Disorders
Young Adult
Issue Date: 2017
Publisher: Springer Nature
Citation: Savulich, 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
Rights: Attribution 4.0 International
Abstract: Naltrexone 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).
Source Title: Translational Psychiatry
URI: https://scholarbank.nus.edu.sg/handle/10635/183541
ISSN: 2158-3188
DOI: 10.1038/tp.2017.34
Rights: Attribution 4.0 International
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