aTranslational Research Center, University Hospital of Psychiatry and Psychotherapy, University of Bern, Bern, Switzerland
bDepartment of Clinical Psychology and Psychotherapy, Institute of Psychology, University of Bern, Bern, Switzerland
Log in to MyKarger to check if you already have access to this content.
Buy FullText & PDF Unlimited re-access via MyKarger Unrestricted printing, no saving restrictions for personal use read more
CHF 38.00 *
EUR 35.00 *
USD 39.00 *
Buy a Karger Article Bundle (KAB) and profit from a discount!
If you would like to redeem your KAB credit, please log in.
Save over 20% compared to the individual article price. Access via DeepDyve Unlimited fulltext viewing Of this article Organize, annotate And mark up articles Printing And downloading restrictions apply Subscribe Access to all articles of the subscribed year(s) guaranteed for 5 years Unlimited re-access via Subscriber Login or MyKarger Unrestricted printing, no saving restrictions for personal use read more Select* The final prices may differ from the prices shown due to specifics of VAT rules.
Article / Publication DetailsFirst-Page Preview
Received: August 27, 2021
Accepted: March 15, 2022
Published online: July 18, 2022
Number of Print Pages: 13
Number of Figures: 3
Number of Tables: 2
ISSN: 0302-282X (Print)
eISSN: 1423-0224 (Online)
For additional information: https://www.karger.com/NPS
AbstractIntroduction: In individuals with alcohol use disorder (AUD), the brain areas underlying cue-induced reactions (e.g., cingulum, striatum, thalamus) and altered activation of these regions have been identified by functional neuroimaging. Neuronal responses to a complex alcohol-related context are yet to investigate. To better understand contextual effects as well as the interplay of cue-induced neural reactions and context exposure, the present study implemented an imagination procedure during functional magnetic resonance imaging (fMRI). Methods: Thirteen patients with AUD and 13 healthy controls completed two rounds of a cue-reactivity paradigm inside an MRI scanner. Two individualized imagination tasks were conducted before each of the two cue reactivity tasks. A 2 (group) × 2 (imagination) × 2 (picture-type) analysis of variance (ANOVA) was performed. Results: The ANOVA revealed a main effect for imagination with higher activation in bilateral thalamus and right caudate nucleus and an interaction effect between imagination and group in right thalamus and left caudate nucleus, due to the patient group reacting stronger during alcohol-related imagination. These structures are involved in relaying sensory information and habit learning. No main or interaction effects of picture type were observed. Conclusions: These results support the view that context effects alter the neural responses in thalamus and nucleus caudatus in patients with AUD, and that imagination tasks are suited to incorporate contextual influences in neurophysiological research designs. Future research needs to investigate whether the failure to observe a picture-type effect was due to limited statistical power and omission to individualize picture set, or whether an imagination procedure interferes with the evocation of picture-type effects.
© 2022 S. Karger AG, Basel
References Evren C, Durkaya M, Evren B, Dalbudak E, Cetin R. Relationship of relapse with impulsivity, novelty seeking and craving in male alcohol-dependent inpatients. Drug Alcohol Rev. 2012;31(1):81–90. Moos RH, Moos BS. Rates and predictors of relapse after natural and treated remission from alcohol use disorders. Addiction. 2006;101(2):212–22. Everitt BJ, Robbins TW. Neural systems of reinforcement for drug addiction: from actions to habits to compulsion. Nat Neurosci. 2005;8(11):1481–9. Valyear MD, Villaruel FR, Chaudhri N. Alcohol-seeking and relapse: a focus on incentive salience and contextual conditioning. Behav Process. 2017;141:26–32. Heinz A, Beck A, Grüsser SM, Grace AA, Wrase J. Identifying the neural circuitry of alcohol craving and relapse vulnerability. Addict Biol. 2009;14(1):108–18. Drummond DC. What does cue-reactivity have to offer clinical research? Addiction. 2000;95 Suppl 2:S129–44. Wrase J, Grüsser SM, Heinz A. [Cue-induced alcohol craving. Neurobiological correlates and clinical relevance]. Nervenarzt. 2006;77(9):1051–3. Ludwig AM, Wikler A, Stark LH. The first drink: psychobiological aspects of craving. Arch Gen Psychiatry. 1974;30(4):539–47. Litten RZ, Ryan ML, Falk DE, Reilly M, Fertig JB, Koob GF. Heterogeneity of alcohol use disorder: understanding mechanisms to advance personalized treatment. Alcohol Clin Exp Res. 2015;39(4):579–84. Wardell JD, Read JP. Does cue context matter? Examining the specificity of cue-related activation of positive and negative alcohol expectancies. Exp Clin Psychopharmacol. 2013;21(6):457–66. Larsen H, Engels RCME, Wiers RW, Granic I, Spijkerman R. Implicit and explicit alcohol cognitions and observed alcohol consumption: three studies in (semi)naturalistic drinking settings. Addiction. 2012;107(8):1420–8. Crombag HS, Bossert JM, Koya E, Shaham Y. Review. Context-induced relapse to drug seeking: a review. Philos Trans R Soc Lond B Biol Sci. 2008;363(1507):3233–43. Fuchs RA, Lasseter HC, Ramirez DR, Xie X. Relapse to drug seeking following prolonged abstinence: the role of environmental stimuli. Drug Discov Today Dis Models. 2008;5(4):251–8. Ghiţă A, Teixidor L, Monras M, Ortega L, Mondon S, Gual A, et al. Identifying triggers of alcohol craving to develop effective virtual environments for cue exposure therapy. Front Psychol. 2019;10:74. Marlatt GA. Taxonomy of high-risk situations for alcohol relapse: evolution and development of a cognitive-behavioral model. Addiction. 1996;91 Suppl:S37–49. Stacy AW, Wiers RW. Implicit cognition and addiction: a tool for explaining paradoxical behavior. Annu Rev Clin Psychol. 2010;6:551–75. Bargh JA, Morsella E. The unconscious mind. Perspect Psychol Sci. 2008;3(1):73–9. Monk RL, Heim D. A systematic review of the Alcohol norms literature: a focus on context. Drugs Educ Prev Policy. 2014;21(4):263–82. Wiers CE, Stelzel C, Gladwin TE, Park SQ, Pawelczack S, Gawron CK, et al. Effects of cognitive bias modification training on neural alcohol cue reactivity in alcohol dependence. Am J Psychiatry. 2015;172(4):335–43. Qureshi A, RLM, Pennington CR, Li X, Leatherbarrow T, R Oulton JR. Visual and auditory contextual cues differentially influence alcohol-related inhibitory control. Adicciones. 2018:1091. Schacht JP, Anton RF, Myrick H. Functional neuroimaging studies of alcohol cue reactivity: a quantitative meta-analysis and systematic review. Addict Biol. 2013;18(1):121–33. Bühler M, Mann K. Alcohol and the human brain: a systematic review of different neuroimaging methods. Alcohol Clin Exp Res. 2011;35(10):1771–93. Sinha R, Li CSR. Imaging stress- and cue-induced drug and alcohol craving: association with relapse and clinical implications. Drug Alcohol Rev. 2007;26(1):25–31. Yalachkov Y, Kaiser J, Naumer MJ. Functional neuroimaging studies in addiction: multisensory drug stimuli and neural cue reactivity. Neurosci Biobehav Rev. 2012;36(2):825–35. Heinz A, Wrase J, Kahnt T, Beck A, Bromand Z, Grüsser SM, et al. Brain activation elicited by affectively positive stimuli is associated with a lower risk of relapse in detoxified alcoholic subjects. Alcohol Clin Exp Res. 2007;31(7):1138–47. George MS, Anton RF, Bloomer C, Teneback C, Drobes DJ, Lorberbaum JP, et al. Activation of prefrontal cortex and anterior thalamus in alcoholic subjects on exposure to alcohol-specific cues. Arch Gen Psychiatry. 2001;58(4):345–52. Bach P, Vollsta Dt-Klein S, Kirsch M, Hoffmann S, Jorde A, Frank J, et al. Increased mesolimbic cue-reactivity in carriers of the mu-opioid-receptor gene OPRM1 A118G polymorphism predicts drinking outcome: a functional imaging study in alcohol dependent subjects. Eur Neuropsychopharmacol. 2015;25(8):1128–35. Beck A, Wüstenberg T, Genauck A, Wrase J, Schlagenhauf F, Smolka MN, et al. Effect of brain structure, brain function, and brain connectivity on relapse in alcohol-dependent patients. Arch Gen Psychiatry. 2012;69(8):842–52. Janes AC, Pizzagalli DA, Richardt S, deB Frederick BD, Chuzi S, Pachas G, et al. brain reactivity to smoking cues prior to smoking cessation predicts ability to maintain tobacco abstinence. Biol Psychiatry. 2010;67(8):722–9. Conklin CA, Tiffany ST. Applying extinction research and theory to cue-exposure addiction treatments. Addiction. 2002;97(2):155–67. Remedios J, Woods C, Tardif C, Janak PH, Chaudhri N. Pavlovian-conditioned alcohol-seeking behavior in rats is invigorated by the interaction between discrete and contextual alcohol cues: implications for relapse. Brain Behav. 2014;4(2):278–89. Chaudhri N, Sahuque LL, Janak PH. Context-induced relapse of conditioned behavioral responding to ethanol cues in rats. Biol Psychiatry. 2008;64(3):203–10. Litt MD, Cooney NL. Inducing craving for alcohol in the laboratory. Alcohol Res Health. 1999;23(3):174–8. Sciascia JM, Reese RM, Janak PH, Chaudhri N. Alcohol-seeking triggered by discrete pavlovian cues is invigorated by alcohol contexts and mediated by glutamate signaling in the basolateral amygdala. Neuropsychopharmacology. 2015;40(12):2801–12. Paris MM, Carter BL, Traylor AC, Bordnick PS, Day SX, Armsworth MW, et al. Cue reactivity in virtual reality: the role of context. Addict Behav. 2011;36(7):696–9. Nees F, Diener C, Smolka MN, Flor H. The role of context in the processing of alcohol-relevant cues. Addict Biol. 2012;17(2):441–51. Boas YAGV. Overview of virtual reality technologies. Proceedings of the interactive multimedia conference. Southhampton: University of Southhampton; 2013. Segawa T, Baudry T, Bourla A, Blanc JV, Peretti CS, Mouchabac S, et al. Virtual reality (VR) in assessment and treatment of addictive disorders: a systematic review. Front Neurosci. 2020;13:1409. Ghita A, Gutierrez-Maldonado J. Applications of virtual reality in individuals with alcohol misuse: a systematic review. Addict Behav. 2018;81:1–11. Durl J, Dietrich T, Pang B, Potter LE, Carter L. Utilising virtual reality in alcohol studies: a systematic review. Health Education J. 2018;77(2):212–25. Kirn T, Echelmeyer L, Engberding M. Imagination in der Verhaltenstherapie. 2nd edn. Heidelberg: Springer; 2015. Meichenbaum D. Warum führt die Anwendung der Imagination in der Psychotherapie zur Veränderung? In: Singer JL, Pope KL, editors. Imaginative Verfahren in der Psychotherapie Paderborn Junfermann; 1999. p. 453–68. Pelchat ML, Johnson A, Chan R, Valdez J, Ragland JD. Images of desire: food-craving activation during fMRI. NeuroImage. 2004;23(4):1486–93. Seo D, Jia ZR, Lacadie CM, Tsou KA, Bergquist K, Sinha R. Sex differences in neural responses to stress and alcohol context cues. Hum Brain Mapp. 2011;32(11):1998–2013. Hamilton M. A rating scale for depression. J Neurol Neurosurg Psychiatry. 1960;23:56–62. Babor TF, de la Fuent JR, Saunders J, Grant M. AUDIT: the alcohol use disorders identification test – guidelines for use in primary health care. Genf: World Health Organisation; 1989. Reinert DF, Allen JP. The alcohol use disorders identification test: an update of research findings. Alcohol Clin Exp Res. 2007;31(2):185–99. Franke GH. Brief symptom inventory von L.R. Derogatis: Deutsches manual. [Brief symptom inventory of L.R. Derogatis – German Manual]. Göttingen: Beltz; 2000. Burren Y, Wapp M, Seitz A, Ballinari P, Moggi F. Obsessive compulsive drinking scale (OCDS-G): psychometrische kennwerte alkoholabhängiger patienten in der Schweiz. Sucht. 2012;58(2):119–25. Fey W, Moggi F, Rohde KB, Michel C, Seitz A, Stein M. Development of stimulus material for research in alcohol use disorders. Int J Methods Psychiatr Res. 2017;26(1):e1527. Grüsser SM, Wrase J, Klein S, Hermann D, Smolka MN, Ruf M, et al. Cue-induced activation of the striatum and medial prefrontal cortex is associated with subsequent relapse in abstinent alcoholics. Psychopharmacology. 2004;175(3):296–302. Wrase J, Grüsser SM, Klein S, Diener C, Hermann D, Flor H, et al. Development of alcohol-associated cues and cue-induced brain activation in alcoholics. Eur Psychiatry. 2002;17(5):287–91. Kaag AM, Wiers RW, de Vries TJ, Pattij T, Goudriaan AE. Striatal alcohol cue-reactivity is stronger in male than female problem drinkers. Eur J Neurosci. 2019;50(3):2264–73. Monk RL, Qureshi A, Heim D. An examination of the extent to which mood and context are associated with real-time alcohol consumption. Drug Alcohol Depend. 2020;208:107880. Claus ED, Ewing SWF, Filbey FM, Sabbineni A, Hutchison KE. Identifying neurobiological phenotypes associated with alcohol use disorder severity. Neuropsychopharmacology. 2011;36(10):2086–96. Jog MS, Kubota Y, Connolly CI, Hillegaart V, Graybiel AM. Building neural representations of habits. Science. 1999;286(5445):1745–9. Berke JD, Hyman SE. Addiction, dopamine, and the molecular mechanisms of memory. Neuron. 2000;25(3):515–32. Graybiel AM, Rauch SL. Toward a neurobiology of obsessive-compulsive disorder. Neuron. 2000;28(2):343–7. Vollstädt-Klein S, Loeber S, Richter A, Kirsch M, Bach P, von der Goltz C, et al. Validating incentive salience with functional magnetic resonance imaging: association between mesolimbic cue reactivity and attentional bias in alcohol-dependent patients. Addict Biol. 2012;17(4):807–16. Carter BL, Tiffany ST. Meta-analysis of cue-reactivity in addiction research. Addiction. 1999;94(3):327–40. Rohde KB, Fey W, Moggi F, Koenig T, Luedi I, Duppenthaler L, et al. Deficient processing of alcohol cues in the addicted brain: evidence from event-related potential microstates. Clin Neurophysiol. 2020;131(9):2224–35. Stein M, Steiner L, Fey W, Conring F, Rieger K, Federspiel A, et al. Alcohol-related context modulates neural correlates of inhibitory control in alcohol dependent patients: preliminary data from an fMRI study using an alcohol-related Go/NoGo-task. Behav Brain Res. 2021;398:112973. Stein M, Fey W, Koenig T, Oehy J, Moggi F. Context-specific inhibition is related to craving in alcohol use disorders: a dangerous imbalance. Alcohol Clin Exp Res. 2018;42(1):69–80. Craik FIM, Lockhart RS. Levels of processing: a framework for memory research. J Verbal Learn Verbal Behav. 1972;11(6):671–84. Hugh M, Anton RF, Xingboa L, Henderson S, Drobes D, Voronin K. Differential brain activity in alcoholics and social drinkers to alcohol cues: relationship to craving. Neuropsychopharmacol. 2004;29:393–402. Del Boca FK, Darkes J, Goldman MS, Smith GT. Advancing the expectancy concept via the interplay between theory and research. Alcohol Clin Exp Res. 2002;26(6):926–35. Rose AK, Field M, Franken IHA, Munafò M. Cue reactivity. Principles of addiction: comprehensive addictive behaviors and disorders. San Diego: Academic Press; 2013. p. 413–23. Vollstädt-Klein S, Loeber S, Kirsch M, Bach P, Richter A, Bühler M, et al. Effects of cue-exposure treatment on neural cue reactivity in alcohol dependence: a randomized trial. Biol Psychiatry. 2011;69(11):1060–6. Lukas SE, Lowen SB, Lindsey KP, Conn N, Tartarini W, Rodolico J, et al. Extended-release naltrexone (XR-NTX) attenuates brain responses to alcohol cues in alcohol-dependent volunteers: a bold FMRI study. Neuro-Image. 2013;78:176–85. Article / Publication DetailsFirst-Page Preview
Received: August 27, 2021
Accepted: March 15, 2022
Published online: July 18, 2022
Number of Print Pages: 13
Number of Figures: 3
Number of Tables: 2
ISSN: 0302-282X (Print)
eISSN: 1423-0224 (Online)
For additional information: https://www.karger.com/NPS
Copyright / Drug Dosage / Disclaimer Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Comments (0)