Pain networks from the inside: Spatiotemporal analysis of brain responses leading from nociception to conscious perception
Conscious perception of painful stimuli needs the contribution of an extensive cortico‐subcortical network, and is completed in less than one second. While initial activities in operculo‐insular and mid‐cingulate cortices have been extensively assessed, the activation timing of most areas supporting...
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description | Conscious perception of painful stimuli needs the contribution of an extensive cortico‐subcortical network, and is completed in less than one second. While initial activities in operculo‐insular and mid‐cingulate cortices have been extensively assessed, the activation timing of most areas supporting conscious pain has barely been studied. Here we used intracranial EEG to investigate the dynamics of 16 brain regions (insular, parietal, prefrontal, cingulate, hippocampal and limbic) during the first second following nociceptive‐specific laser pulses. Three waves of activation could be defined according to their temporal relation with conscious perception, ascertained by voluntary motor responses. Pre‐conscious activities were recorded in the posterior insula, operculum, mid‐cingulate and amygdala. Antero‐insular, prefrontal and posterior parietal activities started later and developed during time‐frames consistent with conscious voluntary reactions. Responses from hippocampus, perigenual and perisplenial cingulate developed latest and persisted well after conscious perception occurred. Nociceptive inputs reach simultaneously sensory and limbic networks, probably through parallel spino‐thalamic and spino‐parabrachial pathways, and the initial limbic activation precedes conscious perception of pain. Access of sensory information to consciousness develops concomitant to fronto‐parietal activity, while late‐occurring responses in the hippocampal region, perigenual and posterior cingulate cortices likely underlie processes linked to memory encoding, self‐awareness and pain modulation. Hum Brain Mapp 37:4301–4315, 2016. © 2016 Wiley Periodicals, Inc. |
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While initial activities in operculo‐insular and mid‐cingulate cortices have been extensively assessed, the activation timing of most areas supporting conscious pain has barely been studied. Here we used intracranial EEG to investigate the dynamics of 16 brain regions (insular, parietal, prefrontal, cingulate, hippocampal and limbic) during the first second following nociceptive‐specific laser pulses. Three waves of activation could be defined according to their temporal relation with conscious perception, ascertained by voluntary motor responses. Pre‐conscious activities were recorded in the posterior insula, operculum, mid‐cingulate and amygdala. Antero‐insular, prefrontal and posterior parietal activities started later and developed during time‐frames consistent with conscious voluntary reactions. Responses from hippocampus, perigenual and perisplenial cingulate developed latest and persisted well after conscious perception occurred. Nociceptive inputs reach simultaneously sensory and limbic networks, probably through parallel spino‐thalamic and spino‐parabrachial pathways, and the initial limbic activation precedes conscious perception of pain. Access of sensory information to consciousness develops concomitant to fronto‐parietal activity, while late‐occurring responses in the hippocampal region, perigenual and posterior cingulate cortices likely underlie processes linked to memory encoding, self‐awareness and pain modulation. 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Brain Mapp</addtitle><description>Conscious perception of painful stimuli needs the contribution of an extensive cortico‐subcortical network, and is completed in less than one second. While initial activities in operculo‐insular and mid‐cingulate cortices have been extensively assessed, the activation timing of most areas supporting conscious pain has barely been studied. Here we used intracranial EEG to investigate the dynamics of 16 brain regions (insular, parietal, prefrontal, cingulate, hippocampal and limbic) during the first second following nociceptive‐specific laser pulses. Three waves of activation could be defined according to their temporal relation with conscious perception, ascertained by voluntary motor responses. Pre‐conscious activities were recorded in the posterior insula, operculum, mid‐cingulate and amygdala. Antero‐insular, prefrontal and posterior parietal activities started later and developed during time‐frames consistent with conscious voluntary reactions. Responses from hippocampus, perigenual and perisplenial cingulate developed latest and persisted well after conscious perception occurred. Nociceptive inputs reach simultaneously sensory and limbic networks, probably through parallel spino‐thalamic and spino‐parabrachial pathways, and the initial limbic activation precedes conscious perception of pain. Access of sensory information to consciousness develops concomitant to fronto‐parietal activity, while late‐occurring responses in the hippocampal region, perigenual and posterior cingulate cortices likely underlie processes linked to memory encoding, self‐awareness and pain modulation. Hum Brain Mapp 37:4301–4315, 2016. © 2016 Wiley Periodicals, Inc.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Anticonvulsants</subject><subject>Anticonvulsants - therapeutic use</subject><subject>Awareness</subject><subject>Awareness - physiology</subject><subject>Brain</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - physiopathology</subject><subject>Brain Mapping</subject><subject>consciousness</subject><subject>Drug Resistant Epilepsy</subject><subject>Drug Resistant Epilepsy - diagnostic imaging</subject><subject>Drug Resistant Epilepsy - drug therapy</subject><subject>Drug Resistant Epilepsy - physiopathology</subject><subject>Electrocorticography</subject><subject>Epilepsies, Partial</subject><subject>Epilepsies, Partial - diagnostic imaging</subject><subject>Epilepsies, Partial - drug therapy</subject><subject>Epilepsies, Partial - physiopathology</subject><subject>Evoked Potentials</subject><subject>Female</subject><subject>human</subject><subject>Humans</subject><subject>intracerebral EEG</subject><subject>Life Sciences</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Motor Activity</subject><subject>Motor Activity - physiology</subject><subject>Neural Pathways</subject><subject>Neural Pathways - diagnostic imaging</subject><subject>Neural Pathways - physiopathology</subject><subject>Neurons and Cognition</subject><subject>Nociceptive Pain</subject><subject>Nociceptive Pain - physiopathology</subject><subject>nociceptive stimulus</subject><subject>pain matrix</subject><subject>Pain Perception</subject><subject>Pain Perception - physiology</subject><subject>Spatio-Temporal Analysis</subject><subject>Young Adult</subject><issn>1065-9471</issn><issn>1097-0193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkktv1DAUhSMEog9Y8AeQJTZ0kdaOn2GBVCroIE0LEiAQG8tJbjpuEzvYmZbh1-Mw0wEqIbGyZX_n-F6fm2VPCD4kGBdHi6o_LCgl-F62S3Apc0xKen_aC56XTJKdbC_GS4wJ4Zg8zHYKSUuCFd3Nfrw31iEH440PVxG1wfdoXACyLtoGXqAPgxmtH6EffDAdMs50q2gj8i2qwiQNEAfvIkTUgWmsu1h7OF_bGoakdWj0qE5Ibf0yogHC5vxR9qA1XYTHm3U_-_Tm9ceTWT5_d_r25Hie14IznFPJWxBVhVnFCZjWcFIWXCmKTasaUjQNJrimSrXQVIIa0yiGiVCpU1UTyeh-9nLtOyyrHpoa3Jha0UOwvQkr7Y3Vf984u9AX_loLJSQvSDI4WBss7shmx3M9neGCyYJxfD2xzzePBf9tCXHUvY01dJ1xkNrXRDHBME8p_QdaCJmCpCqhz-6gl34ZUhYTRUUpiJTyd5118DEGaLfFEqynQdFpUPSvQUns0z8_ZUveTkYCjtbAje1g9W8nPXt1dmuZrxU2jvB9qzDhSguZUtSfz0_1OfvK1dkXrmf0Jx8U14U</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Bastuji, Hélène</creator><creator>Frot, Maud</creator><creator>Perchet, Caroline</creator><creator>Magnin, Michel</creator><creator>Garcia-Larrea, Luis</creator><general>Blackwell Publishing Ltd</general><general>John Wiley & Sons, Inc</general><general>Wiley</general><general>John Wiley and Sons Inc</general><scope>BSCLL</scope><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>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1204-576X</orcidid><orcidid>https://orcid.org/0000-0002-6690-2707</orcidid><orcidid>https://orcid.org/0000-0002-7783-9256</orcidid><orcidid>https://orcid.org/0000-0002-9873-789X</orcidid></search><sort><creationdate>201612</creationdate><title>Pain networks from the inside: Spatiotemporal analysis of brain responses leading from nociception to conscious perception</title><author>Bastuji, Hélène ; Frot, Maud ; Perchet, Caroline ; Magnin, Michel ; Garcia-Larrea, Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6540-375fe6bb04b51eafa519258830af8d12dd010c388fedb63aad8401685018c1743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Anticonvulsants</topic><topic>Anticonvulsants - therapeutic use</topic><topic>Awareness</topic><topic>Awareness - physiology</topic><topic>Brain</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - physiopathology</topic><topic>Brain Mapping</topic><topic>consciousness</topic><topic>Drug Resistant Epilepsy</topic><topic>Drug Resistant Epilepsy - diagnostic imaging</topic><topic>Drug Resistant Epilepsy - drug therapy</topic><topic>Drug Resistant Epilepsy - physiopathology</topic><topic>Electrocorticography</topic><topic>Epilepsies, Partial</topic><topic>Epilepsies, Partial - diagnostic imaging</topic><topic>Epilepsies, Partial - drug therapy</topic><topic>Epilepsies, Partial - physiopathology</topic><topic>Evoked Potentials</topic><topic>Female</topic><topic>human</topic><topic>Humans</topic><topic>intracerebral EEG</topic><topic>Life Sciences</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Motor Activity</topic><topic>Motor Activity - physiology</topic><topic>Neural Pathways</topic><topic>Neural Pathways - diagnostic imaging</topic><topic>Neural Pathways - physiopathology</topic><topic>Neurons and Cognition</topic><topic>Nociceptive Pain</topic><topic>Nociceptive Pain - physiopathology</topic><topic>nociceptive stimulus</topic><topic>pain matrix</topic><topic>Pain Perception</topic><topic>Pain Perception - physiology</topic><topic>Spatio-Temporal Analysis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bastuji, Hélène</creatorcontrib><creatorcontrib>Frot, Maud</creatorcontrib><creatorcontrib>Perchet, Caroline</creatorcontrib><creatorcontrib>Magnin, Michel</creatorcontrib><creatorcontrib>Garcia-Larrea, Luis</creatorcontrib><collection>Istex</collection><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>Hyper Article en Ligne (HAL)</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>Bastuji, Hélène</au><au>Frot, Maud</au><au>Perchet, Caroline</au><au>Magnin, Michel</au><au>Garcia-Larrea, Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pain networks from the inside: Spatiotemporal analysis of brain responses leading from nociception to conscious perception</atitle><jtitle>Human brain mapping</jtitle><addtitle>Hum. Brain Mapp</addtitle><date>2016-12</date><risdate>2016</risdate><volume>37</volume><issue>12</issue><spage>4301</spage><epage>4315</epage><pages>4301-4315</pages><issn>1065-9471</issn><eissn>1097-0193</eissn><abstract>Conscious perception of painful stimuli needs the contribution of an extensive cortico‐subcortical network, and is completed in less than one second. While initial activities in operculo‐insular and mid‐cingulate cortices have been extensively assessed, the activation timing of most areas supporting conscious pain has barely been studied. Here we used intracranial EEG to investigate the dynamics of 16 brain regions (insular, parietal, prefrontal, cingulate, hippocampal and limbic) during the first second following nociceptive‐specific laser pulses. Three waves of activation could be defined according to their temporal relation with conscious perception, ascertained by voluntary motor responses. Pre‐conscious activities were recorded in the posterior insula, operculum, mid‐cingulate and amygdala. Antero‐insular, prefrontal and posterior parietal activities started later and developed during time‐frames consistent with conscious voluntary reactions. Responses from hippocampus, perigenual and perisplenial cingulate developed latest and persisted well after conscious perception occurred. Nociceptive inputs reach simultaneously sensory and limbic networks, probably through parallel spino‐thalamic and spino‐parabrachial pathways, and the initial limbic activation precedes conscious perception of pain. Access of sensory information to consciousness develops concomitant to fronto‐parietal activity, while late‐occurring responses in the hippocampal region, perigenual and posterior cingulate cortices likely underlie processes linked to memory encoding, self‐awareness and pain modulation. Hum Brain Mapp 37:4301–4315, 2016. © 2016 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>27391083</pmid><doi>10.1002/hbm.23310</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-1204-576X</orcidid><orcidid>https://orcid.org/0000-0002-6690-2707</orcidid><orcidid>https://orcid.org/0000-0002-7783-9256</orcidid><orcidid>https://orcid.org/0000-0002-9873-789X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Anticonvulsants Anticonvulsants - therapeutic use Awareness Awareness - physiology Brain Brain - diagnostic imaging Brain - physiopathology Brain Mapping consciousness Drug Resistant Epilepsy Drug Resistant Epilepsy - diagnostic imaging Drug Resistant Epilepsy - drug therapy Drug Resistant Epilepsy - physiopathology Electrocorticography Epilepsies, Partial Epilepsies, Partial - diagnostic imaging Epilepsies, Partial - drug therapy Epilepsies, Partial - physiopathology Evoked Potentials Female human Humans intracerebral EEG Life Sciences Magnetic Resonance Imaging Male Middle Aged Motor Activity Motor Activity - physiology Neural Pathways Neural Pathways - diagnostic imaging Neural Pathways - physiopathology Neurons and Cognition Nociceptive Pain Nociceptive Pain - physiopathology nociceptive stimulus pain matrix Pain Perception Pain Perception - physiology Spatio-Temporal Analysis Young Adult |
title | Pain networks from the inside: Spatiotemporal analysis of brain responses leading from nociception to conscious perception |
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