Dissociating top-down attentional control from selective perception and action
Research into the neural mechanisms of attention has revealed a complex network of brain regions that are involved in the execution of attention-demanding tasks. Recent advances in human neuroimaging now permit investigation of the elementary processes of attention being subserved by specific compon...
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Veröffentlicht in: | Neuropsychologia 2001-01, Vol.39 (12), p.1277-1291 |
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creator | Hopfinger, Joseph B Woldorff, Marty G Fletcher, Evan M Mangun, George R |
description | Research into the neural mechanisms of attention has revealed a complex network of brain regions that are involved in the execution of attention-demanding tasks. Recent advances in human neuroimaging now permit investigation of the elementary processes of attention being subserved by specific components of the brain's attention system. Here we describe recent studies of spatial selective attention that made use of positron emission tomography (PET), functional magnetic resonance imaging (fMRI), and event-related brain potentials (ERPs) to investigate the spatio-temporal dynamics of the attention-related neural activity. We first review the results from an event-related fMRI study that examined the neural mechanisms underlying top-down attentional control versus selective sensory perception. These results defined a fronto-temporal-parietal network involved in the control of spatial attention. Activity in these areas biased the neural activity in sensory brain structures coding the spatial locations of upcoming target stimuli, preceding a modulation of subsequent target processing in visual cortex. We then present preliminary evidence from a fast-rate event-related fMRI study of spatial attention that demonstrates how to disentangle the potentially overlapping hemodynamic responses elicited by temporally adjacent stimuli in studies of attentional control. Finally, we present new analyses from combined neuroimaging (PET) and event-related brain potential (ERP) studies that together reveal the timecourse of activation of brain regions implicated in attentional control and selective perception. |
doi_str_mv | 10.1016/S0028-3932(01)00117-8 |
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We then present preliminary evidence from a fast-rate event-related fMRI study of spatial attention that demonstrates how to disentangle the potentially overlapping hemodynamic responses elicited by temporally adjacent stimuli in studies of attentional control. 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Recent advances in human neuroimaging now permit investigation of the elementary processes of attention being subserved by specific components of the brain's attention system. Here we describe recent studies of spatial selective attention that made use of positron emission tomography (PET), functional magnetic resonance imaging (fMRI), and event-related brain potentials (ERPs) to investigate the spatio-temporal dynamics of the attention-related neural activity. We first review the results from an event-related fMRI study that examined the neural mechanisms underlying top-down attentional control versus selective sensory perception. These results defined a fronto-temporal-parietal network involved in the control of spatial attention. Activity in these areas biased the neural activity in sensory brain structures coding the spatial locations of upcoming target stimuli, preceding a modulation of subsequent target processing in visual cortex. We then present preliminary evidence from a fast-rate event-related fMRI study of spatial attention that demonstrates how to disentangle the potentially overlapping hemodynamic responses elicited by temporally adjacent stimuli in studies of attentional control. Finally, we present new analyses from combined neuroimaging (PET) and event-related brain potential (ERP) studies that together reveal the timecourse of activation of brain regions implicated in attentional control and selective perception.</description><subject>Attention</subject><subject>Attention - physiology</subject><subject>Brain - anatomy & histology</subject><subject>Brain - blood supply</subject><subject>Brain - physiology</subject><subject>Cognition - physiology</subject><subject>Control</subject><subject>Cues</subject><subject>ERP</subject><subject>Evoked Potentials - physiology</subject><subject>fMRI</subject><subject>Frontal Lobe - anatomy & histology</subject><subject>Frontal Lobe - blood supply</subject><subject>Frontal Lobe - physiology</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Parietal Lobe - anatomy & histology</subject><subject>Parietal Lobe - blood supply</subject><subject>Parietal Lobe - physiology</subject><subject>PET</subject><subject>Random Allocation</subject><subject>Space Perception - physiology</subject><subject>Temporal Lobe - anatomy & histology</subject><subject>Temporal Lobe - blood supply</subject><subject>Temporal Lobe - physiology</subject><subject>Time Perception - physiology</subject><subject>Tomography, Emission-Computed</subject><subject>Top–down</subject><subject>Visual Cortex - anatomy & histology</subject><subject>Visual Cortex - blood supply</subject><subject>Visual Cortex - physiology</subject><issn>0028-3932</issn><issn>1873-3514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMlOwzAQQC0EoqXwCaCcEBwCM1mc-IRQWaUKDsDZcp0JMkrjYLtF_D1JW8GR04w0b7bH2DHCBQLyyxeApIxTkSZngOcAiEVc7rAxlkUapzlmu2z8i4zYgfcfAJDlSbnPRog55ynimD3dGO-tNiqY9j0Ktosr-9VGKgRqg7GtaiJt2-BsE9XOLiJPDelgVhR15DR1AxOptoqUHtJDtlerxtPRNk7Y293t6_Qhnj3fP06vZ7HOChFiIbROdH-NKqDiMM84B85J5KCyUoh5zXOEuSiqJOFl3deLOsmVLmsheFoVSTphp5u5nbOfS_JBLozX1DSqJbv0ssDBA-Y9mG9A7az3jmrZObNQ7lsiyEGkXIuUgyUJKNciZdn3nWwXLOcLqv66tuZ64GoDUP_mypCTXhtqNVXG9YZkZc0_K34Am1qCdA</recordid><startdate>20010101</startdate><enddate>20010101</enddate><creator>Hopfinger, Joseph B</creator><creator>Woldorff, Marty G</creator><creator>Fletcher, Evan M</creator><creator>Mangun, George R</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>20010101</creationdate><title>Dissociating top-down attentional control from selective perception and action</title><author>Hopfinger, Joseph B ; Woldorff, Marty G ; Fletcher, Evan M ; Mangun, George R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-99cc2c045a70d60b466066e950a4899bf6510b97d2268f0b47f25ac8f9963d723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Attention</topic><topic>Attention - physiology</topic><topic>Brain - anatomy & histology</topic><topic>Brain - blood supply</topic><topic>Brain - physiology</topic><topic>Cognition - physiology</topic><topic>Control</topic><topic>Cues</topic><topic>ERP</topic><topic>Evoked Potentials - physiology</topic><topic>fMRI</topic><topic>Frontal Lobe - anatomy & histology</topic><topic>Frontal Lobe - blood supply</topic><topic>Frontal Lobe - physiology</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Parietal Lobe - anatomy & histology</topic><topic>Parietal Lobe - blood supply</topic><topic>Parietal Lobe - physiology</topic><topic>PET</topic><topic>Random Allocation</topic><topic>Space Perception - physiology</topic><topic>Temporal Lobe - anatomy & histology</topic><topic>Temporal Lobe - blood supply</topic><topic>Temporal Lobe - physiology</topic><topic>Time Perception - physiology</topic><topic>Tomography, Emission-Computed</topic><topic>Top–down</topic><topic>Visual Cortex - anatomy & histology</topic><topic>Visual Cortex - blood supply</topic><topic>Visual Cortex - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hopfinger, Joseph B</creatorcontrib><creatorcontrib>Woldorff, Marty G</creatorcontrib><creatorcontrib>Fletcher, Evan M</creatorcontrib><creatorcontrib>Mangun, George R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neuropsychologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hopfinger, Joseph B</au><au>Woldorff, Marty G</au><au>Fletcher, Evan M</au><au>Mangun, George R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dissociating top-down attentional control from selective perception and action</atitle><jtitle>Neuropsychologia</jtitle><addtitle>Neuropsychologia</addtitle><date>2001-01-01</date><risdate>2001</risdate><volume>39</volume><issue>12</issue><spage>1277</spage><epage>1291</epage><pages>1277-1291</pages><issn>0028-3932</issn><eissn>1873-3514</eissn><abstract>Research into the neural mechanisms of attention has revealed a complex network of brain regions that are involved in the execution of attention-demanding tasks. Recent advances in human neuroimaging now permit investigation of the elementary processes of attention being subserved by specific components of the brain's attention system. Here we describe recent studies of spatial selective attention that made use of positron emission tomography (PET), functional magnetic resonance imaging (fMRI), and event-related brain potentials (ERPs) to investigate the spatio-temporal dynamics of the attention-related neural activity. We first review the results from an event-related fMRI study that examined the neural mechanisms underlying top-down attentional control versus selective sensory perception. These results defined a fronto-temporal-parietal network involved in the control of spatial attention. Activity in these areas biased the neural activity in sensory brain structures coding the spatial locations of upcoming target stimuli, preceding a modulation of subsequent target processing in visual cortex. We then present preliminary evidence from a fast-rate event-related fMRI study of spatial attention that demonstrates how to disentangle the potentially overlapping hemodynamic responses elicited by temporally adjacent stimuli in studies of attentional control. Finally, we present new analyses from combined neuroimaging (PET) and event-related brain potential (ERP) studies that together reveal the timecourse of activation of brain regions implicated in attentional control and selective perception.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>11566311</pmid><doi>10.1016/S0028-3932(01)00117-8</doi><tpages>15</tpages></addata></record> |
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subjects | Attention Attention - physiology Brain - anatomy & histology Brain - blood supply Brain - physiology Cognition - physiology Control Cues ERP Evoked Potentials - physiology fMRI Frontal Lobe - anatomy & histology Frontal Lobe - blood supply Frontal Lobe - physiology Humans Magnetic Resonance Imaging Parietal Lobe - anatomy & histology Parietal Lobe - blood supply Parietal Lobe - physiology PET Random Allocation Space Perception - physiology Temporal Lobe - anatomy & histology Temporal Lobe - blood supply Temporal Lobe - physiology Time Perception - physiology Tomography, Emission-Computed Top–down Visual Cortex - anatomy & histology Visual Cortex - blood supply Visual Cortex - physiology |
title | Dissociating top-down attentional control from selective perception and action |
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