Short-term plasticity of visuo-haptic object recognition.
Identifieur interne : 000678 ( PubMed/Corpus ); précédent : 000677; suivant : 000679Short-term plasticity of visuo-haptic object recognition.
Auteurs : Tanja Kassuba ; Corinna Klinge ; Cordula Hölig ; Brigitte Röder ; Hartwig R. SiebnerSource :
- Frontiers in psychology [ 1664-1078 ] ; 2014.
Abstract
Functional magnetic resonance imaging (fMRI) studies have provided ample evidence for the involvement of the lateral occipital cortex (LO), fusiform gyrus (FG), and intraparietal sulcus (IPS) in visuo-haptic object integration. Here we applied 30 min of sham (non-effective) or real offline 1 Hz repetitive transcranial magnetic stimulation (rTMS) to perturb neural processing in left LO immediately before subjects performed a visuo-haptic delayed-match-to-sample task during fMRI. In this task, subjects had to match sample (S1) and target (S2) objects presented sequentially within or across vision and/or haptics in both directions (visual-haptic or haptic-visual) and decide whether or not S1 and S2 were the same objects. Real rTMS transiently decreased activity at the site of stimulation and remote regions such as the right LO and bilateral FG during haptic S1 processing. Without affecting behavior, the same stimulation gave rise to relative increases in activation during S2 processing in the right LO, left FG, bilateral IPS, and other regions previously associated with object recognition. Critically, the modality of S2 determined which regions were recruited after rTMS. Relative to sham rTMS, real rTMS induced increased activations during crossmodal congruent matching in the left FG for haptic S2 and the temporal pole for visual S2. In addition, we found stronger activations for incongruent than congruent matching in the right anterior parahippocampus and middle frontal gyrus for crossmodal matching of haptic S2 and in the left FG and bilateral IPS for unimodal matching of visual S2, only after real but not sham rTMS. The results imply that a focal perturbation of the left LO triggers modality-specific interactions between the stimulated left LO and other key regions of object processing possibly to maintain unimpaired object recognition. This suggests that visual and haptic processing engage partially distinct brain networks during visuo-haptic object matching.
DOI: 10.3389/fpsyg.2014.00274
PubMed: 24765082
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Short-term plasticity of visuo-haptic object recognition.</title><author><name sortKey="Kassuba, Tanja" sort="Kassuba, Tanja" uniqKey="Kassuba T" first="Tanja" last="Kassuba">Tanja Kassuba</name><affiliation><nlm:affiliation>Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre Hvidovre, Denmark ; NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Neurology, Christian-Albrechts-University Kiel, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Klinge, Corinna" sort="Klinge, Corinna" uniqKey="Klinge C" first="Corinna" last="Klinge">Corinna Klinge</name><affiliation><nlm:affiliation>NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Psychiatry, Warneford Hospital Oxford, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Holig, Cordula" sort="Holig, Cordula" uniqKey="Holig C" first="Cordula" last="Hölig">Cordula Hölig</name><affiliation><nlm:affiliation>NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Biological Psychology and Neuropsychology, University of Hamburg Hamburg, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Roder, Brigitte" sort="Roder, Brigitte" uniqKey="Roder B" first="Brigitte" last="Röder">Brigitte Röder</name><affiliation><nlm:affiliation>Biological Psychology and Neuropsychology, University of Hamburg Hamburg, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Siebner, Hartwig R" sort="Siebner, Hartwig R" uniqKey="Siebner H" first="Hartwig R" last="Siebner">Hartwig R. Siebner</name><affiliation><nlm:affiliation>Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre Hvidovre, Denmark ; NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Neurology, Christian-Albrechts-University Kiel, Germany.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2014">2014</date><idno type="doi">10.3389/fpsyg.2014.00274</idno><idno type="RBID">pubmed:24765082</idno><idno type="pmid">24765082</idno><idno type="wicri:Area/PubMed/Corpus">000678</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Short-term plasticity of visuo-haptic object recognition.</title><author><name sortKey="Kassuba, Tanja" sort="Kassuba, Tanja" uniqKey="Kassuba T" first="Tanja" last="Kassuba">Tanja Kassuba</name><affiliation><nlm:affiliation>Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre Hvidovre, Denmark ; NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Neurology, Christian-Albrechts-University Kiel, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Klinge, Corinna" sort="Klinge, Corinna" uniqKey="Klinge C" first="Corinna" last="Klinge">Corinna Klinge</name><affiliation><nlm:affiliation>NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Psychiatry, Warneford Hospital Oxford, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Holig, Cordula" sort="Holig, Cordula" uniqKey="Holig C" first="Cordula" last="Hölig">Cordula Hölig</name><affiliation><nlm:affiliation>NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Biological Psychology and Neuropsychology, University of Hamburg Hamburg, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Roder, Brigitte" sort="Roder, Brigitte" uniqKey="Roder B" first="Brigitte" last="Röder">Brigitte Röder</name><affiliation><nlm:affiliation>Biological Psychology and Neuropsychology, University of Hamburg Hamburg, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Siebner, Hartwig R" sort="Siebner, Hartwig R" uniqKey="Siebner H" first="Hartwig R" last="Siebner">Hartwig R. Siebner</name><affiliation><nlm:affiliation>Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre Hvidovre, Denmark ; NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Neurology, Christian-Albrechts-University Kiel, Germany.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Frontiers in psychology</title><idno type="eISSN">1664-1078</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Functional magnetic resonance imaging (fMRI) studies have provided ample evidence for the involvement of the lateral occipital cortex (LO), fusiform gyrus (FG), and intraparietal sulcus (IPS) in visuo-haptic object integration. Here we applied 30 min of sham (non-effective) or real offline 1 Hz repetitive transcranial magnetic stimulation (rTMS) to perturb neural processing in left LO immediately before subjects performed a visuo-haptic delayed-match-to-sample task during fMRI. In this task, subjects had to match sample (S1) and target (S2) objects presented sequentially within or across vision and/or haptics in both directions (visual-haptic or haptic-visual) and decide whether or not S1 and S2 were the same objects. Real rTMS transiently decreased activity at the site of stimulation and remote regions such as the right LO and bilateral FG during haptic S1 processing. Without affecting behavior, the same stimulation gave rise to relative increases in activation during S2 processing in the right LO, left FG, bilateral IPS, and other regions previously associated with object recognition. Critically, the modality of S2 determined which regions were recruited after rTMS. Relative to sham rTMS, real rTMS induced increased activations during crossmodal congruent matching in the left FG for haptic S2 and the temporal pole for visual S2. In addition, we found stronger activations for incongruent than congruent matching in the right anterior parahippocampus and middle frontal gyrus for crossmodal matching of haptic S2 and in the left FG and bilateral IPS for unimodal matching of visual S2, only after real but not sham rTMS. The results imply that a focal perturbation of the left LO triggers modality-specific interactions between the stimulated left LO and other key regions of object processing possibly to maintain unimpaired object recognition. This suggests that visual and haptic processing engage partially distinct brain networks during visuo-haptic object matching.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="PubMed-not-MEDLINE"><PMID Version="1">24765082</PMID><DateCreated><Year>2014</Year><Month>04</Month><Day>25</Day></DateCreated><DateCompleted><Year>2014</Year><Month>04</Month><Day>25</Day></DateCompleted><DateRevised><Year>2015</Year><Month>02</Month><Day>09</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Electronic">1664-1078</ISSN><JournalIssue CitedMedium="Print"><Volume>5</Volume><PubDate><Year>2014</Year></PubDate></JournalIssue><Title>Frontiers in psychology</Title><ISOAbbreviation>Front Psychol</ISOAbbreviation></Journal><ArticleTitle>Short-term plasticity of visuo-haptic object recognition.</ArticleTitle><Pagination><MedlinePgn>274</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.3389/fpsyg.2014.00274</ELocationID><Abstract><AbstractText>Functional magnetic resonance imaging (fMRI) studies have provided ample evidence for the involvement of the lateral occipital cortex (LO), fusiform gyrus (FG), and intraparietal sulcus (IPS) in visuo-haptic object integration. Here we applied 30 min of sham (non-effective) or real offline 1 Hz repetitive transcranial magnetic stimulation (rTMS) to perturb neural processing in left LO immediately before subjects performed a visuo-haptic delayed-match-to-sample task during fMRI. In this task, subjects had to match sample (S1) and target (S2) objects presented sequentially within or across vision and/or haptics in both directions (visual-haptic or haptic-visual) and decide whether or not S1 and S2 were the same objects. Real rTMS transiently decreased activity at the site of stimulation and remote regions such as the right LO and bilateral FG during haptic S1 processing. Without affecting behavior, the same stimulation gave rise to relative increases in activation during S2 processing in the right LO, left FG, bilateral IPS, and other regions previously associated with object recognition. Critically, the modality of S2 determined which regions were recruited after rTMS. Relative to sham rTMS, real rTMS induced increased activations during crossmodal congruent matching in the left FG for haptic S2 and the temporal pole for visual S2. In addition, we found stronger activations for incongruent than congruent matching in the right anterior parahippocampus and middle frontal gyrus for crossmodal matching of haptic S2 and in the left FG and bilateral IPS for unimodal matching of visual S2, only after real but not sham rTMS. The results imply that a focal perturbation of the left LO triggers modality-specific interactions between the stimulated left LO and other key regions of object processing possibly to maintain unimpaired object recognition. This suggests that visual and haptic processing engage partially distinct brain networks during visuo-haptic object matching.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Kassuba</LastName><ForeName>Tanja</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre Hvidovre, Denmark ; NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Neurology, Christian-Albrechts-University Kiel, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Klinge</LastName><ForeName>Corinna</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Psychiatry, Warneford Hospital Oxford, UK.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hölig</LastName><ForeName>Cordula</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Biological Psychology and Neuropsychology, University of Hamburg Hamburg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Röder</LastName><ForeName>Brigitte</ForeName><Initials>B</Initials><AffiliationInfo><Affiliation>Biological Psychology and Neuropsychology, University of Hamburg Hamburg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Siebner</LastName><ForeName>Hartwig R</ForeName><Initials>HR</Initials><AffiliationInfo><Affiliation>Danish Research Centre for Magnetic Resonance, Copenhagen University Hospital Hvidovre Hvidovre, Denmark ; NeuroImageNord/Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf Hamburg, Germany ; Department of Neurology, Christian-Albrechts-University Kiel, Germany.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>04</Month><Day>02</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Front Psychol</MedlineTA><NlmUniqueID>101550902</NlmUniqueID><ISSNLinking>1664-1078</ISSNLinking></MedlineJournalInfo><OtherID Source="NLM">PMC3980106</OtherID><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">functional magnetic resonance imaging</Keyword><Keyword MajorTopicYN="N">haptic perception</Keyword><Keyword MajorTopicYN="N">multisensory interactions</Keyword><Keyword MajorTopicYN="N">object recognition</Keyword><Keyword MajorTopicYN="N">repetitive transcranial magnetic stimulation</Keyword><Keyword MajorTopicYN="N">visual perception</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="ecollection"><Year>2014</Year><Month></Month><Day></Day></PubMedPubDate><PubMedPubDate PubStatus="received"><Year>2014</Year><Month>1</Month><Day>16</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2014</Year><Month>3</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="epublish"><Year>2014</Year><Month>4</Month><Day>02</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2014</Year><Month>4</Month><Day>26</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2014</Year><Month>4</Month><Day>26</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2014</Year><Month>4</Month><Day>26</Day><Hour>6</Hour><Minute>1</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="doi">10.3389/fpsyg.2014.00274</ArticleId><ArticleId IdType="pubmed">24765082</ArticleId><ArticleId IdType="pmc">PMC3980106</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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