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Cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration

Opioid use disorder (OUD) is defined as a compulsion to seek and take opioids, loss of control over intake and the development of a negative emotional state when access to opioids is denied. Using functional magnetic resonance imaging (fMRI) data in a rat model of OUD, we demonstrate that the escala...

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Autores principales: Scarlata, MJ, Keeley, RJ, Carmack, SA, Tsai, P-J, Vendruscolo, JCM, Lu, H, Koob, GF, Vendruscolo, LF, Stein, EA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270679/
https://www.ncbi.nlm.nih.gov/pubmed/37323812
http://dx.doi.org/10.1016/j.addicn.2021.100002
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author Scarlata, MJ
Keeley, RJ
Carmack, SA
Tsai, P-J
Vendruscolo, JCM
Lu, H
Koob, GF
Vendruscolo, LF
Stein, EA
author_facet Scarlata, MJ
Keeley, RJ
Carmack, SA
Tsai, P-J
Vendruscolo, JCM
Lu, H
Koob, GF
Vendruscolo, LF
Stein, EA
author_sort Scarlata, MJ
collection PubMed
description Opioid use disorder (OUD) is defined as a compulsion to seek and take opioids, loss of control over intake and the development of a negative emotional state when access to opioids is denied. Using functional magnetic resonance imaging (fMRI) data in a rat model of OUD, we demonstrate that the escalation of heroin self-administration (SA) and the increased heroin SA following an injection of an opioid receptor antagonist (naloxone) are associated with changes in distinct brain circuits, centered on the cingulate cortex (Cg). Here, SA escalation score was negatively associated with changes in resting state functional connectivity (rsFC) between the Cg and the dorsal striatum. Conversely, increased heroin SA following naloxone injection, was associated with increased connectivity between the Cg and the extended amygdala and hypothalamus. Naloxone-induced increased SA was also positively associated with changes in the amplitude of low frequency fluctuations within the Cg, a measure of spontaneous neuronal activity. Characterizing the distinct brain circuit and behavior changes associated with different facets of addiction increases our understanding of OUD and may provide insight into addiction prevention and treatment.
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spelling pubmed-102706792023-06-15 Cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration Scarlata, MJ Keeley, RJ Carmack, SA Tsai, P-J Vendruscolo, JCM Lu, H Koob, GF Vendruscolo, LF Stein, EA Addict Neurosci Article Opioid use disorder (OUD) is defined as a compulsion to seek and take opioids, loss of control over intake and the development of a negative emotional state when access to opioids is denied. Using functional magnetic resonance imaging (fMRI) data in a rat model of OUD, we demonstrate that the escalation of heroin self-administration (SA) and the increased heroin SA following an injection of an opioid receptor antagonist (naloxone) are associated with changes in distinct brain circuits, centered on the cingulate cortex (Cg). Here, SA escalation score was negatively associated with changes in resting state functional connectivity (rsFC) between the Cg and the dorsal striatum. Conversely, increased heroin SA following naloxone injection, was associated with increased connectivity between the Cg and the extended amygdala and hypothalamus. Naloxone-induced increased SA was also positively associated with changes in the amplitude of low frequency fluctuations within the Cg, a measure of spontaneous neuronal activity. Characterizing the distinct brain circuit and behavior changes associated with different facets of addiction increases our understanding of OUD and may provide insight into addiction prevention and treatment. 2022-03 2021-11-04 /pmc/articles/PMC10270679/ /pubmed/37323812 http://dx.doi.org/10.1016/j.addicn.2021.100002 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) )
spellingShingle Article
Scarlata, MJ
Keeley, RJ
Carmack, SA
Tsai, P-J
Vendruscolo, JCM
Lu, H
Koob, GF
Vendruscolo, LF
Stein, EA
Cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration
title Cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration
title_full Cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration
title_fullStr Cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration
title_full_unstemmed Cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration
title_short Cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration
title_sort cingulate circuits are associated with escalation of heroin use and naloxone-induced increases in heroin self-administration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270679/
https://www.ncbi.nlm.nih.gov/pubmed/37323812
http://dx.doi.org/10.1016/j.addicn.2021.100002
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