Serotonergic modulation of orbitofrontal activity and its relevance for decision making and impulsivity
Background The orbitofrontal cortex seems to play a crucial role in reward‐guided learning and decision making, especially for impulsive choice procedures including delayed reward discounting. The central serotonergic system is closely involved in the regulation of impulsivity, but how the serotoner...
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description | Background
The orbitofrontal cortex seems to play a crucial role in reward‐guided learning and decision making, especially for impulsive choice procedures including delayed reward discounting. The central serotonergic system is closely involved in the regulation of impulsivity, but how the serotonergic firing rate and release, best investigated by the loudness dependence of auditory evoked potentials (LDAEP), interact with orbitofrontal activity is still unknown.
Methods
Twenty healthy volunteers (11 males, 9 females, 31.3 ± 10.6 years old) were studied in a 3T MRI scanner (Philips, Hamburg, Germany) during a delay discounting task, after their LDAEP was recorded using a 32 electrodes EEG machine (Brain Products, Munich, Germany).
Results
Significant positive correlations were only found between the LDAEP and the medial orbitofrontal part of the superior frontal gyrus (SFG/MO) [Δ immediate reward – delayed reward] for the right (r = 0.519; P = 0.019) and left side (r = 0.478; P = 0.033). This relationship was stronger for females compared with males. Orbitofrontal activity was also related to the Barratt Impulsivity Scale.
Conclusions
This study revealed that low serotonergic activity as measured by a strong LDAEP was related to a high fMRI signal intensity of SFG/MO during immediate reward behavior which is related to impulsivity. Since this relationship was only found for the infralimbic medial and not for the middle or lateral part of the orbitofrontal cortex, an exclusive projection tract of the serotonergic system to this cortical region can be assumed to regulate impulsive reward‐orientated decision making. Hum Brain Mapp 38:1507–1517, 2017. © 2016 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/hbm.23468 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6866894</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1872835084</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4768-f5f7d762e65fd1eebada035808d0e864da1bd6da8a37653be417f091ecf5b6b03</originalsourceid><addsrcrecordid>eNqNkU1rFTEUhoMotr268A9IwE27mDaZmXzMRtCiVqi4UNchk5zcpmaSazJzy_33zu3UogWhqwTynIf35EXoFSWnlJD67KofTuum5fIJOqSkExWhXfN0f-es6lpBD9BRKdeEUMoIfY4OaiF5zbrmEK2_QU5jipDX3uAh2Sno0aeIk8Mp935MLqc46oC1Gf3Wjzuso8V-LDhDgK2OBrBLGVswvuwHB_3Tx_VCDZsplNupF-iZ06HAy7tzhX58_PD9_KK6_Prp8_m7y8q0gsvKMSes4DVw5iwF6LXVpGGSSEtA8tZq2ltutdSN4KzpoaXCkY6CcaznPWlW6O3i3Uz9ANZAHLMOapP9oPNOJe3Vvy_RX6l12iouOZddOwuO7wQ5_ZqgjGrwxUAIOkKaiqJS1LJhRD4GndN1gnb7WG8eoNdpynH-iZniTNQNm60rdLJQJqdSMrj73JSofdNqblrdNj2zr_9e9J78U-0MnC3AjQ-w-79JXbz_sih_A0WhtXw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1865723528</pqid></control><display><type>article</type><title>Serotonergic modulation of orbitofrontal activity and its relevance for decision making and impulsivity</title><source>MEDLINE</source><source>Wiley-Blackwell Full Collection</source><source>PubMed Central</source><source>EZB Electronic Journals Library</source><creator>Mavrogiorgou, Paraskevi ; Enzi, Björn ; Klimm, Ann‐Kristin ; Köhler, Elke ; Roser, Patrik ; Norra, Christine ; Juckel, Georg</creator><creatorcontrib>Mavrogiorgou, Paraskevi ; Enzi, Björn ; Klimm, Ann‐Kristin ; Köhler, Elke ; Roser, Patrik ; Norra, Christine ; Juckel, Georg</creatorcontrib><description>Background
The orbitofrontal cortex seems to play a crucial role in reward‐guided learning and decision making, especially for impulsive choice procedures including delayed reward discounting. The central serotonergic system is closely involved in the regulation of impulsivity, but how the serotonergic firing rate and release, best investigated by the loudness dependence of auditory evoked potentials (LDAEP), interact with orbitofrontal activity is still unknown.
Methods
Twenty healthy volunteers (11 males, 9 females, 31.3 ± 10.6 years old) were studied in a 3T MRI scanner (Philips, Hamburg, Germany) during a delay discounting task, after their LDAEP was recorded using a 32 electrodes EEG machine (Brain Products, Munich, Germany).
Results
Significant positive correlations were only found between the LDAEP and the medial orbitofrontal part of the superior frontal gyrus (SFG/MO) [Δ immediate reward – delayed reward] for the right (r = 0.519; P = 0.019) and left side (r = 0.478; P = 0.033). This relationship was stronger for females compared with males. Orbitofrontal activity was also related to the Barratt Impulsivity Scale.
Conclusions
This study revealed that low serotonergic activity as measured by a strong LDAEP was related to a high fMRI signal intensity of SFG/MO during immediate reward behavior which is related to impulsivity. Since this relationship was only found for the infralimbic medial and not for the middle or lateral part of the orbitofrontal cortex, an exclusive projection tract of the serotonergic system to this cortical region can be assumed to regulate impulsive reward‐orientated decision making. Hum Brain Mapp 38:1507–1517, 2017. © 2016 Wiley Periodicals, Inc.</description><identifier>ISSN: 1065-9471</identifier><identifier>EISSN: 1097-0193</identifier><identifier>DOI: 10.1002/hbm.23468</identifier><identifier>PMID: 27862593</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Acoustic Stimulation ; Adult ; Cues ; Decision Making - physiology ; delay discounting ; Delay Discounting - physiology ; Electroencephalography ; Evoked Potentials, Auditory - physiology ; Female ; Humans ; Image Processing, Computer-Assisted ; Impulsive Behavior - physiology ; LDAEP ; Magnetic Resonance Imaging ; Male ; orbitofrontal cortex ; Oxygen ; Prefrontal Cortex - diagnostic imaging ; Prefrontal Cortex - physiology ; Psychoacoustics ; Psychometrics ; Psychomotor Performance ; Reaction Time ; serotonin ; Young Adult</subject><ispartof>Human brain mapping, 2017-03, Vol.38 (3), p.1507-1517</ispartof><rights>2016 Wiley Periodicals, Inc.</rights><rights>2017 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4768-f5f7d762e65fd1eebada035808d0e864da1bd6da8a37653be417f091ecf5b6b03</citedby><cites>FETCH-LOGICAL-c4768-f5f7d762e65fd1eebada035808d0e864da1bd6da8a37653be417f091ecf5b6b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6866894/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6866894/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,27924,27925,45574,45575,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27862593$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mavrogiorgou, Paraskevi</creatorcontrib><creatorcontrib>Enzi, Björn</creatorcontrib><creatorcontrib>Klimm, Ann‐Kristin</creatorcontrib><creatorcontrib>Köhler, Elke</creatorcontrib><creatorcontrib>Roser, Patrik</creatorcontrib><creatorcontrib>Norra, Christine</creatorcontrib><creatorcontrib>Juckel, Georg</creatorcontrib><title>Serotonergic modulation of orbitofrontal activity and its relevance for decision making and impulsivity</title><title>Human brain mapping</title><addtitle>Hum Brain Mapp</addtitle><description>Background
The orbitofrontal cortex seems to play a crucial role in reward‐guided learning and decision making, especially for impulsive choice procedures including delayed reward discounting. The central serotonergic system is closely involved in the regulation of impulsivity, but how the serotonergic firing rate and release, best investigated by the loudness dependence of auditory evoked potentials (LDAEP), interact with orbitofrontal activity is still unknown.
Methods
Twenty healthy volunteers (11 males, 9 females, 31.3 ± 10.6 years old) were studied in a 3T MRI scanner (Philips, Hamburg, Germany) during a delay discounting task, after their LDAEP was recorded using a 32 electrodes EEG machine (Brain Products, Munich, Germany).
Results
Significant positive correlations were only found between the LDAEP and the medial orbitofrontal part of the superior frontal gyrus (SFG/MO) [Δ immediate reward – delayed reward] for the right (r = 0.519; P = 0.019) and left side (r = 0.478; P = 0.033). This relationship was stronger for females compared with males. Orbitofrontal activity was also related to the Barratt Impulsivity Scale.
Conclusions
This study revealed that low serotonergic activity as measured by a strong LDAEP was related to a high fMRI signal intensity of SFG/MO during immediate reward behavior which is related to impulsivity. Since this relationship was only found for the infralimbic medial and not for the middle or lateral part of the orbitofrontal cortex, an exclusive projection tract of the serotonergic system to this cortical region can be assumed to regulate impulsive reward‐orientated decision making. Hum Brain Mapp 38:1507–1517, 2017. © 2016 Wiley Periodicals, Inc.</description><subject>Acoustic Stimulation</subject><subject>Adult</subject><subject>Cues</subject><subject>Decision Making - physiology</subject><subject>delay discounting</subject><subject>Delay Discounting - physiology</subject><subject>Electroencephalography</subject><subject>Evoked Potentials, Auditory - physiology</subject><subject>Female</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Impulsive Behavior - physiology</subject><subject>LDAEP</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>orbitofrontal cortex</subject><subject>Oxygen</subject><subject>Prefrontal Cortex - diagnostic imaging</subject><subject>Prefrontal Cortex - physiology</subject><subject>Psychoacoustics</subject><subject>Psychometrics</subject><subject>Psychomotor Performance</subject><subject>Reaction Time</subject><subject>serotonin</subject><subject>Young Adult</subject><issn>1065-9471</issn><issn>1097-0193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1rFTEUhoMotr268A9IwE27mDaZmXzMRtCiVqi4UNchk5zcpmaSazJzy_33zu3UogWhqwTynIf35EXoFSWnlJD67KofTuum5fIJOqSkExWhXfN0f-es6lpBD9BRKdeEUMoIfY4OaiF5zbrmEK2_QU5jipDX3uAh2Sno0aeIk8Mp935MLqc46oC1Gf3Wjzuso8V-LDhDgK2OBrBLGVswvuwHB_3Tx_VCDZsplNupF-iZ06HAy7tzhX58_PD9_KK6_Prp8_m7y8q0gsvKMSes4DVw5iwF6LXVpGGSSEtA8tZq2ltutdSN4KzpoaXCkY6CcaznPWlW6O3i3Uz9ANZAHLMOapP9oPNOJe3Vvy_RX6l12iouOZddOwuO7wQ5_ZqgjGrwxUAIOkKaiqJS1LJhRD4GndN1gnb7WG8eoNdpynH-iZniTNQNm60rdLJQJqdSMrj73JSofdNqblrdNj2zr_9e9J78U-0MnC3AjQ-w-79JXbz_sih_A0WhtXw</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>Mavrogiorgou, Paraskevi</creator><creator>Enzi, Björn</creator><creator>Klimm, Ann‐Kristin</creator><creator>Köhler, Elke</creator><creator>Roser, Patrik</creator><creator>Norra, Christine</creator><creator>Juckel, Georg</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201703</creationdate><title>Serotonergic modulation of orbitofrontal activity and its relevance for decision making and impulsivity</title><author>Mavrogiorgou, Paraskevi ; Enzi, Björn ; Klimm, Ann‐Kristin ; Köhler, Elke ; Roser, Patrik ; Norra, Christine ; Juckel, Georg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4768-f5f7d762e65fd1eebada035808d0e864da1bd6da8a37653be417f091ecf5b6b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acoustic Stimulation</topic><topic>Adult</topic><topic>Cues</topic><topic>Decision Making - physiology</topic><topic>delay discounting</topic><topic>Delay Discounting - physiology</topic><topic>Electroencephalography</topic><topic>Evoked Potentials, Auditory - physiology</topic><topic>Female</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Impulsive Behavior - physiology</topic><topic>LDAEP</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>orbitofrontal cortex</topic><topic>Oxygen</topic><topic>Prefrontal Cortex - diagnostic imaging</topic><topic>Prefrontal Cortex - physiology</topic><topic>Psychoacoustics</topic><topic>Psychometrics</topic><topic>Psychomotor Performance</topic><topic>Reaction Time</topic><topic>serotonin</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mavrogiorgou, Paraskevi</creatorcontrib><creatorcontrib>Enzi, Björn</creatorcontrib><creatorcontrib>Klimm, Ann‐Kristin</creatorcontrib><creatorcontrib>Köhler, Elke</creatorcontrib><creatorcontrib>Roser, Patrik</creatorcontrib><creatorcontrib>Norra, Christine</creatorcontrib><creatorcontrib>Juckel, Georg</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Human brain mapping</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mavrogiorgou, Paraskevi</au><au>Enzi, Björn</au><au>Klimm, Ann‐Kristin</au><au>Köhler, Elke</au><au>Roser, Patrik</au><au>Norra, Christine</au><au>Juckel, Georg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serotonergic modulation of orbitofrontal activity and its relevance for decision making and impulsivity</atitle><jtitle>Human brain mapping</jtitle><addtitle>Hum Brain Mapp</addtitle><date>2017-03</date><risdate>2017</risdate><volume>38</volume><issue>3</issue><spage>1507</spage><epage>1517</epage><pages>1507-1517</pages><issn>1065-9471</issn><eissn>1097-0193</eissn><abstract>Background
The orbitofrontal cortex seems to play a crucial role in reward‐guided learning and decision making, especially for impulsive choice procedures including delayed reward discounting. The central serotonergic system is closely involved in the regulation of impulsivity, but how the serotonergic firing rate and release, best investigated by the loudness dependence of auditory evoked potentials (LDAEP), interact with orbitofrontal activity is still unknown.
Methods
Twenty healthy volunteers (11 males, 9 females, 31.3 ± 10.6 years old) were studied in a 3T MRI scanner (Philips, Hamburg, Germany) during a delay discounting task, after their LDAEP was recorded using a 32 electrodes EEG machine (Brain Products, Munich, Germany).
Results
Significant positive correlations were only found between the LDAEP and the medial orbitofrontal part of the superior frontal gyrus (SFG/MO) [Δ immediate reward – delayed reward] for the right (r = 0.519; P = 0.019) and left side (r = 0.478; P = 0.033). This relationship was stronger for females compared with males. Orbitofrontal activity was also related to the Barratt Impulsivity Scale.
Conclusions
This study revealed that low serotonergic activity as measured by a strong LDAEP was related to a high fMRI signal intensity of SFG/MO during immediate reward behavior which is related to impulsivity. Since this relationship was only found for the infralimbic medial and not for the middle or lateral part of the orbitofrontal cortex, an exclusive projection tract of the serotonergic system to this cortical region can be assumed to regulate impulsive reward‐orientated decision making. Hum Brain Mapp 38:1507–1517, 2017. © 2016 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>27862593</pmid><doi>10.1002/hbm.23468</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acoustic Stimulation Adult Cues Decision Making - physiology delay discounting Delay Discounting - physiology Electroencephalography Evoked Potentials, Auditory - physiology Female Humans Image Processing, Computer-Assisted Impulsive Behavior - physiology LDAEP Magnetic Resonance Imaging Male orbitofrontal cortex Oxygen Prefrontal Cortex - diagnostic imaging Prefrontal Cortex - physiology Psychoacoustics Psychometrics Psychomotor Performance Reaction Time serotonin Young Adult |
title | Serotonergic modulation of orbitofrontal activity and its relevance for decision making and impulsivity |
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