Frontal and Parietal Lobe Activation during Transitive Inference in Humans
Identifieur interne : 002675 ( Istex/Corpus ); précédent : 002674; suivant : 002676Frontal and Parietal Lobe Activation during Transitive Inference in Humans
Auteurs : Bettina D. Acuna ; James C. Eliassen ; John P. Donoghue ; Jerome N. SanesSource :
- Cerebral Cortex [ 1047-3211 ] ; 2002-12.
Abstract
Cortical areas engaged in knowledge manipulation during reasoning were identified with functional magnetic resonance imaging (MRI) while participants performed transitive inference (TI) on an ordered list of 11 items (e.g. if A < B and B < C, then A < C). Initially, participants learned a list of arbitrarily ordered visual shapes. Learning occurred by exposure to pairs of list items that were adjacent in the sequence. Subsequently, functional MR images were acquired as participants performed TI on non-adjacent sequence items. Control tasks consisted of height comparisons (HT) and passive viewing (VIS). Comparison of the TI task with the HT task identified activation resulting from TI, termed ‘reasoning’, while controlling for rule application, decision processes, perception, and movement, collectively termed ‘support processes’. The HT–VIS comparison revealed activation related to support processes. The TI reasoning network included bilateral prefrontal cortex (PFC), pre-supplementary motor area (preSMA), premotor area (PMA), insula, precuneus, and lateral posterior parietal cortex. By contrast, cortical regions activated by support processes included the bilateral supplementary motor area (SMA), primary motor cortex (M1), somatic sensory cortices, and right PMA. These results emphasize the role of a prefrontal–parietal network in manipulating information to form new knowledge based on familiar facts. The findings also demonstrate PFC activation beyond short-term memory to include mental operations associated with reasoning.
Url:
DOI: 10.1093/cercor/12.12.1312
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Acuna</name><affiliation><mods:affiliation>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</mods:affiliation></affiliation></author><author><name sortKey="Eliassen, James C" sort="Eliassen, James C" uniqKey="Eliassen J" first="James C." last="Eliassen">James C. Eliassen</name><affiliation><mods:affiliation>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</mods:affiliation></affiliation></author><author><name sortKey="Donoghue, John P" sort="Donoghue, John P" uniqKey="Donoghue J" first="John P." last="Donoghue">John P. Donoghue</name><affiliation><mods:affiliation>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</mods:affiliation></affiliation></author><author><name sortKey="Sanes, Jerome N" sort="Sanes, Jerome N" uniqKey="Sanes J" first="Jerome N." last="Sanes">Jerome N. Sanes</name><affiliation><mods:affiliation>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Cerebral Cortex</title><title level="j" type="abbrev">Cereb. Cortex</title><idno type="ISSN">1047-3211</idno><idno type="eISSN">1460-2199</idno><imprint><publisher>Oxford University Press</publisher><date type="published" when="2002-12">2002-12</date><biblScope unit="volume">12</biblScope><biblScope unit="issue">12</biblScope><biblScope unit="page" from="1312">1312</biblScope><biblScope unit="page" to="1321">1321</biblScope></imprint><idno type="ISSN">1047-3211</idno></series><idno type="istex">03B893B050084B29448BE6067BE099F451CACADD</idno><idno type="DOI">10.1093/cercor/12.12.1312</idno><idno type="PII">1460-2199</idno><idno type="local">0121312</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">1047-3211</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Cortical areas engaged in knowledge manipulation during reasoning were identified with functional magnetic resonance imaging (MRI) while participants performed transitive inference (TI) on an ordered list of 11 items (e.g. if A < B and B < C, then A < C). Initially, participants learned a list of arbitrarily ordered visual shapes. Learning occurred by exposure to pairs of list items that were adjacent in the sequence. Subsequently, functional MR images were acquired as participants performed TI on non-adjacent sequence items. Control tasks consisted of height comparisons (HT) and passive viewing (VIS). Comparison of the TI task with the HT task identified activation resulting from TI, termed ‘reasoning’, while controlling for rule application, decision processes, perception, and movement, collectively termed ‘support processes’. The HT–VIS comparison revealed activation related to support processes. The TI reasoning network included bilateral prefrontal cortex (PFC), pre-supplementary motor area (preSMA), premotor area (PMA), insula, precuneus, and lateral posterior parietal cortex. By contrast, cortical regions activated by support processes included the bilateral supplementary motor area (SMA), primary motor cortex (M1), somatic sensory cortices, and right PMA. These results emphasize the role of a prefrontal–parietal network in manipulating information to form new knowledge based on familiar facts. The findings also demonstrate PFC activation beyond short-term memory to include mental operations associated with reasoning.</div></front></TEI><istex><corpusName>oup</corpusName><author><json:item><name>Bettina D. Acuna</name><affiliations><json:string>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</json:string></affiliations></json:item><json:item><name>James C. Eliassen</name><affiliations><json:string>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</json:string></affiliations></json:item><json:item><name>John P. Donoghue</name><affiliations><json:string>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</json:string></affiliations></json:item><json:item><name>Jerome N. Sanes</name><affiliations><json:string>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</json:string></affiliations></json:item></author><language><json:string>eng</json:string></language><abstract>Cortical areas engaged in knowledge manipulation during reasoning were identified with functional magnetic resonance imaging (MRI) while participants performed transitive inference (TI) on an ordered list of 11 items (e.g. if A > B and B > C, then A > C). Initially, participants learned a list of arbitrarily ordered visual shapes. Learning occurred by exposure to pairs of list items that were adjacent in the sequence. Subsequently, functional MR images were acquired as participants performed TI on non-adjacent sequence items. Control tasks consisted of height comparisons (HT) and passive viewing (VIS). Comparison of the TI task with the HT task identified activation resulting from TI, termed ‘reasoning’, while controlling for rule application, decision processes, perception, and movement, collectively termed ‘support processes’. The HT–VIS comparison revealed activation related to support processes. The TI reasoning network included bilateral prefrontal cortex (PFC), pre-supplementary motor area (preSMA), premotor area (PMA), insula, precuneus, and lateral posterior parietal cortex. By contrast, cortical regions activated by support processes included the bilateral supplementary motor area (SMA), primary motor cortex (M1), somatic sensory cortices, and right PMA. These results emphasize the role of a prefrontal–parietal network in manipulating information to form new knowledge based on familiar facts. 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Cortex</title><idno type="pISSN">1047-3211</idno><idno type="eISSN">1460-2199</idno><imprint><publisher>Oxford University Press</publisher><date type="published" when="2002-12"></date><biblScope unit="volume">12</biblScope><biblScope unit="issue">12</biblScope><biblScope unit="page" from="1312">1312</biblScope><biblScope unit="page" to="1321">1321</biblScope></imprint></monogr><idno type="istex">03B893B050084B29448BE6067BE099F451CACADD</idno><idno type="DOI">10.1093/cercor/12.12.1312</idno><idno type="PII">1460-2199</idno><idno type="local">0121312</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2002</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Cortical areas engaged in knowledge manipulation during reasoning were identified with functional magnetic resonance imaging (MRI) while participants performed transitive inference (TI) on an ordered list of 11 items (e.g. if A < B and B < C, then A < C). Initially, participants learned a list of arbitrarily ordered visual shapes. Learning occurred by exposure to pairs of list items that were adjacent in the sequence. Subsequently, functional MR images were acquired as participants performed TI on non-adjacent sequence items. Control tasks consisted of height comparisons (HT) and passive viewing (VIS). Comparison of the TI task with the HT task identified activation resulting from TI, termed ‘reasoning’, while controlling for rule application, decision processes, perception, and movement, collectively termed ‘support processes’. The HT–VIS comparison revealed activation related to support processes. The TI reasoning network included bilateral prefrontal cortex (PFC), pre-supplementary motor area (preSMA), premotor area (PMA), insula, precuneus, and lateral posterior parietal cortex. By contrast, cortical regions activated by support processes included the bilateral supplementary motor area (SMA), primary motor cortex (M1), somatic sensory cortices, and right PMA. These results emphasize the role of a prefrontal–parietal network in manipulating information to form new knowledge based on familiar facts. 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Cortex</abbrev-journal-title><issn pub-type="ppub">1047-3211</issn><issn pub-type="epub">1460-2199</issn><publisher><publisher-name>Oxford University Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.1093/cercor/12.12.1312</article-id><article-id pub-id-type="other">0121312</article-id><article-id pub-id-type="pii">1460-2199</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Frontal and Parietal Lobe Activation during Transitive Inference in Humans</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Acuna</surname><given-names>Bettina D.</given-names></name><xref rid="AFF1">1</xref><xref rid="FN2">2</xref></contrib><contrib contrib-type="author"><name><surname>Eliassen</surname><given-names>James C.</given-names></name><xref rid="AFF1">1</xref></contrib><contrib contrib-type="author"><name><surname>Donoghue</surname><given-names>John P.</given-names></name><xref rid="AFF1">1</xref></contrib><contrib contrib-type="author"><name><surname>Sanes</surname><given-names>Jerome N.</given-names></name><xref rid="AFF1">1</xref></contrib><aff id="AFF1"><label>1</label>Department of Neuroscience, Brown Medical School, Providence, RI 02912 USA</aff></contrib-group><author-notes><corresp>Address correspondence to Dr Jerome N. Sanes, Department of Neuroscience, Brown Medical School, Box 1953, Providence, RI 02912, USA. Email: <ext-link xlink:href="Jerome_Sanes@Brown.edu" ext-link-type="email">Jerome_Sanes@Brown.edu</ext-link>.</corresp></author-notes><pub-date pub-type="ppub"><month>12</month><year>2002</year></pub-date><volume>12</volume><issue>12</issue><fpage>1312</fpage><lpage>1321</lpage><permissions><copyright-statement>© Oxford University Press</copyright-statement><copyright-year>2002</copyright-year></permissions><abstract xml:lang="en"><p>Cortical areas engaged in knowledge manipulation during reasoning were identified with functional magnetic resonance imaging (MRI) while participants performed transitive inference (TI) on an ordered list of 11 items (e.g. if A < B and B < C, then A < C). Initially, participants learned a list of arbitrarily ordered visual shapes. Learning occurred by exposure to pairs of list items that were adjacent in the sequence. Subsequently, functional MR images were acquired as participants performed TI on non-adjacent sequence items. Control tasks consisted of height comparisons (HT) and passive viewing (VIS). Comparison of the TI task with the HT task identified activation resulting from TI, termed ‘reasoning’, while controlling for rule application, decision processes, perception, and movement, collectively termed ‘support processes’. The HT–VIS comparison revealed activation related to support processes. The TI reasoning network included bilateral prefrontal cortex (PFC), pre-supplementary motor area (preSMA), premotor area (PMA), insula, precuneus, and lateral posterior parietal cortex. By contrast, cortical regions activated by support processes included the bilateral supplementary motor area (SMA), primary motor cortex (M1), somatic sensory cortices, and right PMA. 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