Somato-motor haptic processing in posterior inner perisylvian region (SII/pIC) of the macaque monkey.
Identifieur interne : 000800 ( PubMed/Checkpoint ); précédent : 000799; suivant : 000801Somato-motor haptic processing in posterior inner perisylvian region (SII/pIC) of the macaque monkey.
Auteurs : Hiroaki Ishida [Italie] ; Luca Fornia ; Laura Clara Grandi ; Maria Alessandra Umiltà ; Vittorio GalleseSource :
- PloS one [ 1932-6203 ] ; 2013.
English descriptors
- KwdEn :
- MESH :
- physiology : Hand, Hand Strength, Motor Activity, Neurons, Parietal Lobe.
- Animals, Evoked Potentials, Fingers, Macaca, Male, Photic Stimulation, Psychomotor Performance.
Abstract
The posterior inner perisylvian region including the secondary somatosensory cortex (area SII) and the adjacent region of posterior insular cortex (pIC) has been implicated in haptic processing by integrating somato-motor information during hand-manipulation, both in humans and in non-human primates. However, motor-related properties during hand-manipulation are still largely unknown. To investigate a motor-related activity in the hand region of SII/pIC, two macaque monkeys were trained to perform a hand-manipulation task, requiring 3 different grip types (precision grip, finger exploration, side grip) both in light and in dark conditions. Our results showed that 70% (n = 33/48) of task related neurons within SII/pIC were only activated during monkeys' active hand-manipulation. Of those 33 neurons, 15 (45%) began to discharge before hand-target contact, while the remaining neurons were tonically active after contact. Thirty-percent (n = 15/48) of studied neurons responded to both passive somatosensory stimulation and to the motor task. A consistent percentage of task-related neurons in SII/pIC was selectively activated during finger exploration (FE) and precision grasping (PG) execution, suggesting they play a pivotal role in control skilled finger movements. Furthermore, hand-manipulation-related neurons also responded when visual feedback was absent in the dark. Altogether, our results suggest that somato-motor neurons in SII/pIC likely contribute to haptic processing from the initial to the final phase of grasping and object manipulation. Such motor-related activity could also provide the somato-motor binding principle enabling the translation of diachronic somatosensory inputs into a coherent image of the explored object.
DOI: 10.1371/journal.pone.0069931
PubMed: 23936121
Affiliations:
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Somato-motor haptic processing in posterior inner perisylvian region (SII/pIC) of the macaque monkey.</title><author><name sortKey="Ishida, Hiroaki" sort="Ishida, Hiroaki" uniqKey="Ishida H" first="Hiroaki" last="Ishida">Hiroaki Ishida</name><affiliation wicri:level="1"><nlm:affiliation>Italian Institute of Technology (IIT), Brain Center for Motor and Social Cognition (BCSMC), Parma, Italy. hiroaki.ishida@iit.it</nlm:affiliation><country xml:lang="fr">Italie</country><wicri:regionArea>Italian Institute of Technology (IIT), Brain Center for Motor and Social Cognition (BCSMC), Parma</wicri:regionArea><wicri:noRegion>Parma</wicri:noRegion></affiliation></author><author><name sortKey="Fornia, Luca" sort="Fornia, Luca" uniqKey="Fornia L" first="Luca" last="Fornia">Luca Fornia</name></author><author><name sortKey="Grandi, Laura Clara" sort="Grandi, Laura Clara" uniqKey="Grandi L" first="Laura Clara" last="Grandi">Laura Clara Grandi</name></author><author><name sortKey="Umilta, Maria Alessandra" sort="Umilta, Maria Alessandra" uniqKey="Umilta M" first="Maria Alessandra" last="Umiltà">Maria Alessandra Umiltà</name></author><author><name sortKey="Gallese, Vittorio" sort="Gallese, Vittorio" uniqKey="Gallese V" first="Vittorio" last="Gallese">Vittorio Gallese</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2013">2013</date><idno type="doi">10.1371/journal.pone.0069931</idno><idno type="RBID">pubmed:23936121</idno><idno type="pmid">23936121</idno><idno type="wicri:Area/PubMed/Corpus">000898</idno><idno type="wicri:Area/PubMed/Curation">000898</idno><idno type="wicri:Area/PubMed/Checkpoint">000800</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Somato-motor haptic processing in posterior inner perisylvian region (SII/pIC) of the macaque monkey.</title><author><name sortKey="Ishida, Hiroaki" sort="Ishida, Hiroaki" uniqKey="Ishida H" first="Hiroaki" last="Ishida">Hiroaki Ishida</name><affiliation wicri:level="1"><nlm:affiliation>Italian Institute of Technology (IIT), Brain Center for Motor and Social Cognition (BCSMC), Parma, Italy. hiroaki.ishida@iit.it</nlm:affiliation><country xml:lang="fr">Italie</country><wicri:regionArea>Italian Institute of Technology (IIT), Brain Center for Motor and Social Cognition (BCSMC), Parma</wicri:regionArea><wicri:noRegion>Parma</wicri:noRegion></affiliation></author><author><name sortKey="Fornia, Luca" sort="Fornia, Luca" uniqKey="Fornia L" first="Luca" last="Fornia">Luca Fornia</name></author><author><name sortKey="Grandi, Laura Clara" sort="Grandi, Laura Clara" uniqKey="Grandi L" first="Laura Clara" last="Grandi">Laura Clara Grandi</name></author><author><name sortKey="Umilta, Maria Alessandra" sort="Umilta, Maria Alessandra" uniqKey="Umilta M" first="Maria Alessandra" last="Umiltà">Maria Alessandra Umiltà</name></author><author><name sortKey="Gallese, Vittorio" sort="Gallese, Vittorio" uniqKey="Gallese V" first="Vittorio" last="Gallese">Vittorio Gallese</name></author></analytic><series><title level="j">PloS one</title><idno type="eISSN">1932-6203</idno><imprint><date when="2013" type="published">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Evoked Potentials</term><term>Fingers</term><term>Hand (physiology)</term><term>Hand Strength (physiology)</term><term>Macaca</term><term>Male</term><term>Motor Activity (physiology)</term><term>Neurons (physiology)</term><term>Parietal Lobe (physiology)</term><term>Photic Stimulation</term><term>Psychomotor Performance</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Hand</term><term>Hand Strength</term><term>Motor Activity</term><term>Neurons</term><term>Parietal Lobe</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Evoked Potentials</term><term>Fingers</term><term>Macaca</term><term>Male</term><term>Photic Stimulation</term><term>Psychomotor Performance</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The posterior inner perisylvian region including the secondary somatosensory cortex (area SII) and the adjacent region of posterior insular cortex (pIC) has been implicated in haptic processing by integrating somato-motor information during hand-manipulation, both in humans and in non-human primates. However, motor-related properties during hand-manipulation are still largely unknown. To investigate a motor-related activity in the hand region of SII/pIC, two macaque monkeys were trained to perform a hand-manipulation task, requiring 3 different grip types (precision grip, finger exploration, side grip) both in light and in dark conditions. Our results showed that 70% (n = 33/48) of task related neurons within SII/pIC were only activated during monkeys' active hand-manipulation. Of those 33 neurons, 15 (45%) began to discharge before hand-target contact, while the remaining neurons were tonically active after contact. Thirty-percent (n = 15/48) of studied neurons responded to both passive somatosensory stimulation and to the motor task. A consistent percentage of task-related neurons in SII/pIC was selectively activated during finger exploration (FE) and precision grasping (PG) execution, suggesting they play a pivotal role in control skilled finger movements. Furthermore, hand-manipulation-related neurons also responded when visual feedback was absent in the dark. Altogether, our results suggest that somato-motor neurons in SII/pIC likely contribute to haptic processing from the initial to the final phase of grasping and object manipulation. Such motor-related activity could also provide the somato-motor binding principle enabling the translation of diachronic somatosensory inputs into a coherent image of the explored object.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">23936121</PMID><DateCreated><Year>2013</Year><Month>08</Month><Day>12</Day></DateCreated><DateCompleted><Year>2014</Year><Month>04</Month><Day>01</Day></DateCompleted><DateRevised><Year>2015</Year><Month>04</Month><Day>23</Day></DateRevised><Article PubModel="Electronic-Print"><Journal><ISSN IssnType="Electronic">1932-6203</ISSN><JournalIssue CitedMedium="Internet"><Volume>8</Volume><Issue>7</Issue><PubDate><Year>2013</Year></PubDate></JournalIssue><Title>PloS one</Title><ISOAbbreviation>PLoS ONE</ISOAbbreviation></Journal><ArticleTitle>Somato-motor haptic processing in posterior inner perisylvian region (SII/pIC) of the macaque monkey.</ArticleTitle><Pagination><MedlinePgn>e69931</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1371/journal.pone.0069931</ELocationID><Abstract><AbstractText>The posterior inner perisylvian region including the secondary somatosensory cortex (area SII) and the adjacent region of posterior insular cortex (pIC) has been implicated in haptic processing by integrating somato-motor information during hand-manipulation, both in humans and in non-human primates. However, motor-related properties during hand-manipulation are still largely unknown. To investigate a motor-related activity in the hand region of SII/pIC, two macaque monkeys were trained to perform a hand-manipulation task, requiring 3 different grip types (precision grip, finger exploration, side grip) both in light and in dark conditions. Our results showed that 70% (n = 33/48) of task related neurons within SII/pIC were only activated during monkeys' active hand-manipulation. Of those 33 neurons, 15 (45%) began to discharge before hand-target contact, while the remaining neurons were tonically active after contact. Thirty-percent (n = 15/48) of studied neurons responded to both passive somatosensory stimulation and to the motor task. A consistent percentage of task-related neurons in SII/pIC was selectively activated during finger exploration (FE) and precision grasping (PG) execution, suggesting they play a pivotal role in control skilled finger movements. Furthermore, hand-manipulation-related neurons also responded when visual feedback was absent in the dark. Altogether, our results suggest that somato-motor neurons in SII/pIC likely contribute to haptic processing from the initial to the final phase of grasping and object manipulation. Such motor-related activity could also provide the somato-motor binding principle enabling the translation of diachronic somatosensory inputs into a coherent image of the explored object.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ishida</LastName><ForeName>Hiroaki</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Italian Institute of Technology (IIT), Brain Center for Motor and Social Cognition (BCSMC), Parma, Italy. hiroaki.ishida@iit.it</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Fornia</LastName><ForeName>Luca</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Grandi</LastName><ForeName>Laura Clara</ForeName><Initials>LC</Initials></Author><Author ValidYN="Y"><LastName>Umiltà</LastName><ForeName>Maria Alessandra</ForeName><Initials>MA</Initials></Author><Author ValidYN="Y"><LastName>Gallese</LastName><ForeName>Vittorio</ForeName><Initials>V</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2013</Year><Month>07</Month><Day>30</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>PLoS One</MedlineTA><NlmUniqueID>101285081</NlmUniqueID><ISSNLinking>1932-6203</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Biol Cybern. 2002 Aug;87(2):116-40</RefSource><PMID Version="1">12181587</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Nat Neurosci. 2002 Nov;5(11):1217-25</RefSource><PMID Version="1">12368806</PMID></CommentsCorrections><CommentsCorrections 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UI="D008251">Macaca</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D009043">Motor Activity</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D009474">Neurons</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D010296">Parietal Lobe</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D010775">Photic Stimulation</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D011597">Psychomotor Performance</DescriptorName></MeshHeading></MeshHeadingList><OtherID Source="NLM">PMC3728371</OtherID></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="ppublish"><Year>2013</Year><Month></Month><Day></Day></PubMedPubDate><PubMedPubDate PubStatus="received"><Year>2013</Year><Month>2</Month><Day>28</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2013</Year><Month>6</Month><Day>12</Day></PubMedPubDate><PubMedPubDate PubStatus="epublish"><Year>2013</Year><Month>7</Month><Day>30</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2013</Year><Month>8</Month><Day>13</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2013</Year><Month>8</Month><Day>13</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2014</Year><Month>4</Month><Day>2</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="doi">10.1371/journal.pone.0069931</ArticleId><ArticleId IdType="pii">PONE-D-13-09301</ArticleId><ArticleId IdType="pubmed">23936121</ArticleId><ArticleId IdType="pmc">PMC3728371</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Italie</li></country></list><tree><noCountry><name sortKey="Fornia, Luca" sort="Fornia, Luca" uniqKey="Fornia L" first="Luca" last="Fornia">Luca Fornia</name><name sortKey="Gallese, Vittorio" sort="Gallese, Vittorio" uniqKey="Gallese V" first="Vittorio" last="Gallese">Vittorio Gallese</name><name sortKey="Grandi, Laura Clara" sort="Grandi, Laura Clara" uniqKey="Grandi L" first="Laura Clara" last="Grandi">Laura Clara Grandi</name><name sortKey="Umilta, Maria Alessandra" sort="Umilta, Maria Alessandra" uniqKey="Umilta M" first="Maria Alessandra" last="Umiltà">Maria Alessandra Umiltà</name></noCountry><country name="Italie"><noRegion><name sortKey="Ishida, Hiroaki" sort="Ishida, Hiroaki" uniqKey="Ishida H" first="Hiroaki" last="Ishida">Hiroaki Ishida</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous 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