Cargando…
Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking
Expectancy of physical and social pleasure (PSP) promotes excessive drinking despite the potential aversive effects of misuse, suggesting an imbalance in the response to reward and pain in alcohol seeking. Here, we investigated the competing roles of the reward and pain circuits in PSP expectancy an...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341762/ https://www.ncbi.nlm.nih.gov/pubmed/32636394 http://dx.doi.org/10.1038/s41398-020-00909-z |
_version_ | 1783555303099334656 |
---|---|
author | Le, Thang M. Zhornitsky, Simon Zhang, Sheng Li, Chiang-Shan R. |
author_facet | Le, Thang M. Zhornitsky, Simon Zhang, Sheng Li, Chiang-Shan R. |
author_sort | Le, Thang M. |
collection | PubMed |
description | Expectancy of physical and social pleasure (PSP) promotes excessive drinking despite the potential aversive effects of misuse, suggesting an imbalance in the response to reward and pain in alcohol seeking. Here, we investigated the competing roles of the reward and pain circuits in PSP expectancy and problem drinking in humans. Using fMRI data during resting (n = 180) and during alcohol cue exposure (n = 71), we examined the antagonistic effects of the reward-related medial orbitofrontal cortex (mOFC) and pain-related periaqueductal gray (PAG) connectivities on PSP expectancy and drinking severity. The two regions’ connectivity maps and strengths were characterized to assess their shared substrates and net relationship with PSP expectancy. We evaluated mediation and path models to further delineate how mOFC and PAG connectivities interacted through the shared substrates to differentially impact expectancy and alcohol use. During resting, whole-brain regressions showed mOFC connectivity in positive and PAG connectivity in negative association with PSP scores, with convergence in the precentral gyrus (PrCG). Notably, greater PAG-PrCG relative to mOFC-PrCG connectivity strength predicted lower PSP expectancy. During the alcohol cue exposure task, the net strength of the PAG vs. mOFC cue-elicited connectivity with the occipital cortex again negatively predicted PSP expectancy. Finally, mediation and path models revealed that the PAG and mOFC connectivities indirectly and antagonistically modulated problem drinking via their opposing influences on expectancy and craving. Thus, the pain and reward circuits exhibit functional antagonism such that the mOFC connectivity increases expectancy of drinking pleasure whereas the PAG serves to counter that effect. |
format | Online Article Text |
id | pubmed-7341762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73417622020-07-09 Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking Le, Thang M. Zhornitsky, Simon Zhang, Sheng Li, Chiang-Shan R. Transl Psychiatry Article Expectancy of physical and social pleasure (PSP) promotes excessive drinking despite the potential aversive effects of misuse, suggesting an imbalance in the response to reward and pain in alcohol seeking. Here, we investigated the competing roles of the reward and pain circuits in PSP expectancy and problem drinking in humans. Using fMRI data during resting (n = 180) and during alcohol cue exposure (n = 71), we examined the antagonistic effects of the reward-related medial orbitofrontal cortex (mOFC) and pain-related periaqueductal gray (PAG) connectivities on PSP expectancy and drinking severity. The two regions’ connectivity maps and strengths were characterized to assess their shared substrates and net relationship with PSP expectancy. We evaluated mediation and path models to further delineate how mOFC and PAG connectivities interacted through the shared substrates to differentially impact expectancy and alcohol use. During resting, whole-brain regressions showed mOFC connectivity in positive and PAG connectivity in negative association with PSP scores, with convergence in the precentral gyrus (PrCG). Notably, greater PAG-PrCG relative to mOFC-PrCG connectivity strength predicted lower PSP expectancy. During the alcohol cue exposure task, the net strength of the PAG vs. mOFC cue-elicited connectivity with the occipital cortex again negatively predicted PSP expectancy. Finally, mediation and path models revealed that the PAG and mOFC connectivities indirectly and antagonistically modulated problem drinking via their opposing influences on expectancy and craving. Thus, the pain and reward circuits exhibit functional antagonism such that the mOFC connectivity increases expectancy of drinking pleasure whereas the PAG serves to counter that effect. Nature Publishing Group UK 2020-07-07 /pmc/articles/PMC7341762/ /pubmed/32636394 http://dx.doi.org/10.1038/s41398-020-00909-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Le, Thang M. Zhornitsky, Simon Zhang, Sheng Li, Chiang-Shan R. Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking |
title | Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking |
title_full | Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking |
title_fullStr | Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking |
title_full_unstemmed | Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking |
title_short | Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking |
title_sort | pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341762/ https://www.ncbi.nlm.nih.gov/pubmed/32636394 http://dx.doi.org/10.1038/s41398-020-00909-z |
work_keys_str_mv | AT lethangm painandrewardcircuitsantagonisticallymodulatealcoholexpectancytoregulatedrinking AT zhornitskysimon painandrewardcircuitsantagonisticallymodulatealcoholexpectancytoregulatedrinking AT zhangsheng painandrewardcircuitsantagonisticallymodulatealcoholexpectancytoregulatedrinking AT lichiangshanr painandrewardcircuitsantagonisticallymodulatealcoholexpectancytoregulatedrinking |