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The neurochemical substrates of habitual and goal-directed control
Our daily decisions are governed by the arbitration between goal-directed and habitual strategies. However, the neurochemical basis of this arbitration is unclear. We assessed the contribution of dopaminergic, serotonergic, and opioidergic systems to this balance across reward and loss domains. Thir...
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Published in: | Translational psychiatry 2020-03, Vol.10 (1), p.84-84, Article 84 |
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description | Our daily decisions are governed by the arbitration between goal-directed and habitual strategies. However, the neurochemical basis of this arbitration is unclear. We assessed the contribution of dopaminergic, serotonergic, and opioidergic systems to this balance across reward and loss domains. Thirty-nine participants (17 healthy controls, 15 patients with pathological gambling, and 7 with binge eating disorder) underwent positron emission tomography (PET) imaging with [
18
F]FDOPA, [
11
C]MADAM and [
11
C]carfentanil to assess presynaptic dopamine, and serotonin transporter and mu-opioid receptor binding potential. Separately, participants completed a modified two-step task, which quantifies the degree to which decision-making is influenced by goal-directed or habitual strategies. All participants completed a version with reward outcomes; healthy controls additionally completed a version with loss outcomes. In the context of rewarding outcomes, we found that greater serotonin transporter binding potential in prefrontal regions was associated with habitual control, while greater serotonin transporter binding potential in the putamen was marginally associated with goal-directed control; however, the findings were no longer significant when controlling for the opposing valence (loss). In blocks with loss outcomes, we found that the opioidergic system, specifically greater [
11
C]carfentanil binding potential, was positively associated with goal-directed control and negatively associated with habit-directed control. Our findings illuminate the complex neurochemical basis of goal-directed and habitual behavior, implicating differential roles for prefrontal and subcortical serotonin in decision-making across healthy and pathological populations. |
doi_str_mv | 10.1038/s41398-020-0762-5 |
format | article |
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18
F]FDOPA, [
11
C]MADAM and [
11
C]carfentanil to assess presynaptic dopamine, and serotonin transporter and mu-opioid receptor binding potential. Separately, participants completed a modified two-step task, which quantifies the degree to which decision-making is influenced by goal-directed or habitual strategies. All participants completed a version with reward outcomes; healthy controls additionally completed a version with loss outcomes. In the context of rewarding outcomes, we found that greater serotonin transporter binding potential in prefrontal regions was associated with habitual control, while greater serotonin transporter binding potential in the putamen was marginally associated with goal-directed control; however, the findings were no longer significant when controlling for the opposing valence (loss). In blocks with loss outcomes, we found that the opioidergic system, specifically greater [
11
C]carfentanil binding potential, was positively associated with goal-directed control and negatively associated with habit-directed control. Our findings illuminate the complex neurochemical basis of goal-directed and habitual behavior, implicating differential roles for prefrontal and subcortical serotonin in decision-making across healthy and pathological populations.</description><identifier>ISSN: 2158-3188</identifier><identifier>EISSN: 2158-3188</identifier><identifier>DOI: 10.1038/s41398-020-0762-5</identifier><identifier>PMID: 32127520</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>59/78 ; 631/378 ; 631/477/2811 ; Behavioral Sciences ; Biological Psychology ; Decision making ; Medicine ; Medicine & Public Health ; Neurosciences ; Pharmacotherapy ; Psychiatry ; Serotonin</subject><ispartof>Translational psychiatry, 2020-03, Vol.10 (1), p.84-84, Article 84</ispartof><rights>The Author(s) 2020</rights><rights>This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-d8cb98e3b1241852c51b0020aab87499963fd423249e74648bf644ac44084f03</citedby><cites>FETCH-LOGICAL-c498t-d8cb98e3b1241852c51b0020aab87499963fd423249e74648bf644ac44084f03</cites><orcidid>0000-0002-9281-3417 ; 0000-0002-3446-7093</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2370447300/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2370447300?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,75096</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32127520$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Voon, Valerie</creatorcontrib><creatorcontrib>Joutsa, Juho</creatorcontrib><creatorcontrib>Majuri, Joonas</creatorcontrib><creatorcontrib>Baek, Kwangyeol</creatorcontrib><creatorcontrib>Nord, Camilla L.</creatorcontrib><creatorcontrib>Arponen, Eveliina</creatorcontrib><creatorcontrib>Forsback, Sarita</creatorcontrib><creatorcontrib>Kaasinen, Valtteri</creatorcontrib><title>The neurochemical substrates of habitual and goal-directed control</title><title>Translational psychiatry</title><addtitle>Transl Psychiatry</addtitle><addtitle>Transl Psychiatry</addtitle><description>Our daily decisions are governed by the arbitration between goal-directed and habitual strategies. However, the neurochemical basis of this arbitration is unclear. We assessed the contribution of dopaminergic, serotonergic, and opioidergic systems to this balance across reward and loss domains. Thirty-nine participants (17 healthy controls, 15 patients with pathological gambling, and 7 with binge eating disorder) underwent positron emission tomography (PET) imaging with [
18
F]FDOPA, [
11
C]MADAM and [
11
C]carfentanil to assess presynaptic dopamine, and serotonin transporter and mu-opioid receptor binding potential. Separately, participants completed a modified two-step task, which quantifies the degree to which decision-making is influenced by goal-directed or habitual strategies. All participants completed a version with reward outcomes; healthy controls additionally completed a version with loss outcomes. In the context of rewarding outcomes, we found that greater serotonin transporter binding potential in prefrontal regions was associated with habitual control, while greater serotonin transporter binding potential in the putamen was marginally associated with goal-directed control; however, the findings were no longer significant when controlling for the opposing valence (loss). In blocks with loss outcomes, we found that the opioidergic system, specifically greater [
11
C]carfentanil binding potential, was positively associated with goal-directed control and negatively associated with habit-directed control. 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Joutsa, Juho ; Majuri, Joonas ; Baek, Kwangyeol ; Nord, Camilla L. ; Arponen, Eveliina ; Forsback, Sarita ; Kaasinen, Valtteri</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-d8cb98e3b1241852c51b0020aab87499963fd423249e74648bf644ac44084f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>59/78</topic><topic>631/378</topic><topic>631/477/2811</topic><topic>Behavioral Sciences</topic><topic>Biological Psychology</topic><topic>Decision making</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neurosciences</topic><topic>Pharmacotherapy</topic><topic>Psychiatry</topic><topic>Serotonin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Voon, Valerie</creatorcontrib><creatorcontrib>Joutsa, Juho</creatorcontrib><creatorcontrib>Majuri, Joonas</creatorcontrib><creatorcontrib>Baek, Kwangyeol</creatorcontrib><creatorcontrib>Nord, Camilla L.</creatorcontrib><creatorcontrib>Arponen, Eveliina</creatorcontrib><creatorcontrib>Forsback, Sarita</creatorcontrib><creatorcontrib>Kaasinen, Valtteri</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Translational psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Voon, Valerie</au><au>Joutsa, Juho</au><au>Majuri, Joonas</au><au>Baek, Kwangyeol</au><au>Nord, Camilla L.</au><au>Arponen, Eveliina</au><au>Forsback, Sarita</au><au>Kaasinen, Valtteri</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The neurochemical substrates of habitual and goal-directed control</atitle><jtitle>Translational psychiatry</jtitle><stitle>Transl Psychiatry</stitle><addtitle>Transl Psychiatry</addtitle><date>2020-03-03</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>84</spage><epage>84</epage><pages>84-84</pages><artnum>84</artnum><issn>2158-3188</issn><eissn>2158-3188</eissn><abstract>Our daily decisions are governed by the arbitration between goal-directed and habitual strategies. 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18
F]FDOPA, [
11
C]MADAM and [
11
C]carfentanil to assess presynaptic dopamine, and serotonin transporter and mu-opioid receptor binding potential. Separately, participants completed a modified two-step task, which quantifies the degree to which decision-making is influenced by goal-directed or habitual strategies. All participants completed a version with reward outcomes; healthy controls additionally completed a version with loss outcomes. In the context of rewarding outcomes, we found that greater serotonin transporter binding potential in prefrontal regions was associated with habitual control, while greater serotonin transporter binding potential in the putamen was marginally associated with goal-directed control; however, the findings were no longer significant when controlling for the opposing valence (loss). In blocks with loss outcomes, we found that the opioidergic system, specifically greater [
11
C]carfentanil binding potential, was positively associated with goal-directed control and negatively associated with habit-directed control. Our findings illuminate the complex neurochemical basis of goal-directed and habitual behavior, implicating differential roles for prefrontal and subcortical serotonin in decision-making across healthy and pathological populations.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32127520</pmid><doi>10.1038/s41398-020-0762-5</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9281-3417</orcidid><orcidid>https://orcid.org/0000-0002-3446-7093</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 59/78 631/378 631/477/2811 Behavioral Sciences Biological Psychology Decision making Medicine Medicine & Public Health Neurosciences Pharmacotherapy Psychiatry Serotonin |
title | The neurochemical substrates of habitual and goal-directed control |
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