Primary sensory and motor cortex activities during voluntary and passive ankle mobilization by the SHADE orthosis
This study investigates cortical involvement during ankle passive mobilization in healthy subjects, and is part of a pilot study on stroke patient rehabilitation. Magnetoencephalographic signals from the primary sensorimotor areas devoted to the lower limb were collected together with simultaneous e...
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creator | Pittaccio, Simone Zappasodi, Filippo Viscuso, Stefano Mastrolilli, Francesca Ercolani, Matilde Passarelli, Francesco Molteni, Franco Besseghini, Stefano Rossini, Paolo Maria Tecchio, Franca |
description | This study investigates cortical involvement during ankle passive mobilization in healthy subjects, and is part of a pilot study on stroke patient rehabilitation. Magnetoencephalographic signals from the primary sensorimotor areas devoted to the lower limb were collected together with simultaneous electromyographic activities from tibialis anterior (TA). This was done bilaterally, on seven healthy subjects (aged 29 ± 7), during rest, left and right passive ankle dorsiflexion (imparted through the SHADE orthosis, O‐PM, or neuromuscular electrical stimulation, NMES‐PM), and during active isometric contraction (IC‐AM). The effects of focussing attention on ankle passive movements were considered. Primary sensory (FSS1) and motor (FSM1) area activities were discriminated by the Functional Source Separation algorithm. Only contralateral FSS1 was recruited by common peroneal nerve stimulation and only contralateral FSM1 displayed coherence with TA muscular activity. FSM1 showed higher power of gamma rhythms (33–90 Hz) than FSS1. Both sources displayed higher beta (14–32 Hz) and gamma powers in the left than in the right hemisphere. Both sources displayed a bilateral reduction of beta power during IC‐AM with respect to rest. Only FSS1 beta band power reduced during O‐PM. No beta band modulation was observed of either source during NMES‐PM. Mutual FSS1‐FSM1 coherence in gamma2 band (61–90 Hz) showed a slight trend towards an increase when focussing attention during O‐PM. Somatosensory and motor counterparts of lower limb cortical representations were discriminated in both hemispheres. SHADE was effective in generating repeatable dorsiflexion and inducing primary sensory involvement similarly to voluntary movement. Hum Brain Mapp, 2010. © 2010 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/hbm.20998 |
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Magnetoencephalographic signals from the primary sensorimotor areas devoted to the lower limb were collected together with simultaneous electromyographic activities from tibialis anterior (TA). This was done bilaterally, on seven healthy subjects (aged 29 ± 7), during rest, left and right passive ankle dorsiflexion (imparted through the SHADE orthosis, O‐PM, or neuromuscular electrical stimulation, NMES‐PM), and during active isometric contraction (IC‐AM). The effects of focussing attention on ankle passive movements were considered. Primary sensory (FSS1) and motor (FSM1) area activities were discriminated by the Functional Source Separation algorithm. Only contralateral FSS1 was recruited by common peroneal nerve stimulation and only contralateral FSM1 displayed coherence with TA muscular activity. FSM1 showed higher power of gamma rhythms (33–90 Hz) than FSS1. Both sources displayed higher beta (14–32 Hz) and gamma powers in the left than in the right hemisphere. Both sources displayed a bilateral reduction of beta power during IC‐AM with respect to rest. Only FSS1 beta band power reduced during O‐PM. No beta band modulation was observed of either source during NMES‐PM. Mutual FSS1‐FSM1 coherence in gamma2 band (61–90 Hz) showed a slight trend towards an increase when focussing attention during O‐PM. Somatosensory and motor counterparts of lower limb cortical representations were discriminated in both hemispheres. SHADE was effective in generating repeatable dorsiflexion and inducing primary sensory involvement similarly to voluntary movement. Hum Brain Mapp, 2010. © 2010 Wiley‐Liss, Inc.</description><identifier>ISSN: 1065-9471</identifier><identifier>ISSN: 1097-0193</identifier><identifier>EISSN: 1097-0193</identifier><identifier>DOI: 10.1002/hbm.20998</identifier><identifier>PMID: 20336689</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Algorithms ; Ankle ; Ankle Joint - physiology ; ankle movement ; Attention ; Biological and medical sciences ; Brain Mapping ; Cortex (motor) ; Cortex (somatosensory) ; Electric Stimulation ; Electrical stimuli ; Electromyography ; EMG ; Female ; Fundamental and applied biological sciences. Psychology ; Hemispheric laterality ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Limbs ; Magnetoencephalography ; Male ; Medical sciences ; Motion Therapy, Continuous Passive ; Motor Cortex - physiology ; Movement - physiology ; Muscle contraction ; Muscle Contraction - physiology ; Nervous system ; Orthotic Devices ; peroneal nerve ; Pilot Projects ; Radiodiagnosis. Nmr imagery. Nmr spectrometry ; Rehabilitation ; Rhythms ; sensorimotor ; sensorimotor system ; Shade ; Somatosensory Cortex - physiology ; Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors ; Stroke ; Vertebrates: nervous system and sense organs</subject><ispartof>Human brain mapping, 2011-01, Vol.32 (1), p.60-70</ispartof><rights>Copyright © 2010 Wiley‐Liss, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Hum Brain Mapp, 2010. © 2010 Wiley-Liss, Inc.</rights><rights>Copyright © 2010 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6088-185dacb12ac6fe3a97cc39f84af7e035c71ad7e0f4d2d7e75893837905a133aa3</citedby><cites>FETCH-LOGICAL-c6088-185dacb12ac6fe3a97cc39f84af7e035c71ad7e0f4d2d7e75893837905a133aa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6870115/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6870115/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,27903,27904,45553,45554,53770,53772</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23652920$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20336689$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pittaccio, Simone</creatorcontrib><creatorcontrib>Zappasodi, Filippo</creatorcontrib><creatorcontrib>Viscuso, Stefano</creatorcontrib><creatorcontrib>Mastrolilli, Francesca</creatorcontrib><creatorcontrib>Ercolani, Matilde</creatorcontrib><creatorcontrib>Passarelli, Francesco</creatorcontrib><creatorcontrib>Molteni, Franco</creatorcontrib><creatorcontrib>Besseghini, Stefano</creatorcontrib><creatorcontrib>Rossini, Paolo Maria</creatorcontrib><creatorcontrib>Tecchio, Franca</creatorcontrib><title>Primary sensory and motor cortex activities during voluntary and passive ankle mobilization by the SHADE orthosis</title><title>Human brain mapping</title><addtitle>Hum. Brain Mapp</addtitle><description>This study investigates cortical involvement during ankle passive mobilization in healthy subjects, and is part of a pilot study on stroke patient rehabilitation. Magnetoencephalographic signals from the primary sensorimotor areas devoted to the lower limb were collected together with simultaneous electromyographic activities from tibialis anterior (TA). This was done bilaterally, on seven healthy subjects (aged 29 ± 7), during rest, left and right passive ankle dorsiflexion (imparted through the SHADE orthosis, O‐PM, or neuromuscular electrical stimulation, NMES‐PM), and during active isometric contraction (IC‐AM). The effects of focussing attention on ankle passive movements were considered. Primary sensory (FSS1) and motor (FSM1) area activities were discriminated by the Functional Source Separation algorithm. Only contralateral FSS1 was recruited by common peroneal nerve stimulation and only contralateral FSM1 displayed coherence with TA muscular activity. FSM1 showed higher power of gamma rhythms (33–90 Hz) than FSS1. Both sources displayed higher beta (14–32 Hz) and gamma powers in the left than in the right hemisphere. Both sources displayed a bilateral reduction of beta power during IC‐AM with respect to rest. Only FSS1 beta band power reduced during O‐PM. No beta band modulation was observed of either source during NMES‐PM. Mutual FSS1‐FSM1 coherence in gamma2 band (61–90 Hz) showed a slight trend towards an increase when focussing attention during O‐PM. Somatosensory and motor counterparts of lower limb cortical representations were discriminated in both hemispheres. SHADE was effective in generating repeatable dorsiflexion and inducing primary sensory involvement similarly to voluntary movement. Hum Brain Mapp, 2010. © 2010 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Algorithms</subject><subject>Ankle</subject><subject>Ankle Joint - physiology</subject><subject>ankle movement</subject><subject>Attention</subject><subject>Biological and medical sciences</subject><subject>Brain Mapping</subject><subject>Cortex (motor)</subject><subject>Cortex (somatosensory)</subject><subject>Electric Stimulation</subject><subject>Electrical stimuli</subject><subject>Electromyography</subject><subject>EMG</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hemispheric laterality</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Limbs</subject><subject>Magnetoencephalography</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Motion Therapy, Continuous Passive</subject><subject>Motor Cortex - physiology</subject><subject>Movement - physiology</subject><subject>Muscle contraction</subject><subject>Muscle Contraction - physiology</subject><subject>Nervous system</subject><subject>Orthotic Devices</subject><subject>peroneal nerve</subject><subject>Pilot Projects</subject><subject>Radiodiagnosis. Nmr imagery. Nmr spectrometry</subject><subject>Rehabilitation</subject><subject>Rhythms</subject><subject>sensorimotor</subject><subject>sensorimotor system</subject><subject>Shade</subject><subject>Somatosensory Cortex - physiology</subject><subject>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</subject><subject>Stroke</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>1065-9471</issn><issn>1097-0193</issn><issn>1097-0193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk1v1DAQhi0EomXhwB9AkRBCHNLacRzbl0rtUrqIlg8By9GaOE7XbRJv7WRh-fV4yXb5kBC-zEh-5h3PvEboMcEHBOPscFG2BxmWUtxB-wRLnmIi6d1NXrBU5pzsoQchXGFMCMPkPtrLMKVFIeQ-unnvbQt-nQTTBRcjdFXSut75RDvfm28J6N6ubG9NSKrB2-4yWblm6HrYwksIwa5MzK8bE0tL29jv0FvXJeU66Rcm-Tg7fnmaRLWFCzY8RPdqaIJ5tI0T9PnV6afpLD1_d_Z6enye6gILkRLBKtAlyUAXtaEgudZU1iKHmhtMmeYEqpjVeZXFyJmQVFAuMQNCKQCdoKNRdzmUram06XoPjVqO8yoHVv1509mFunQrVQi-WVQUeL4V8O5mMKFXrQ3aNA10xg1BCSFIBHPyf5KIHGc0ngl6-hd55QbfxT0owginjDKeRerFSGnvQvCm3r2aYLVxXEXH1U_HI_vk9zF35K3FEXi2BSBoaGoPnbbhF0cLlslIT9DhyH21jVn_u6OanVzctk7HChviR9lVgL9WBaecqS9vz9QJfzO_mM-n6gP9AVlg03E</recordid><startdate>201101</startdate><enddate>201101</enddate><creator>Pittaccio, Simone</creator><creator>Zappasodi, Filippo</creator><creator>Viscuso, Stefano</creator><creator>Mastrolilli, Francesca</creator><creator>Ercolani, Matilde</creator><creator>Passarelli, Francesco</creator><creator>Molteni, Franco</creator><creator>Besseghini, Stefano</creator><creator>Rossini, Paolo Maria</creator><creator>Tecchio, Franca</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><general>John Wiley & Sons, Inc</general><scope>BSCLL</scope><scope>IQODW</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>5PM</scope></search><sort><creationdate>201101</creationdate><title>Primary sensory and motor cortex activities during voluntary and passive ankle mobilization by the SHADE orthosis</title><author>Pittaccio, Simone ; Zappasodi, Filippo ; Viscuso, Stefano ; Mastrolilli, Francesca ; Ercolani, Matilde ; Passarelli, Francesco ; Molteni, Franco ; Besseghini, Stefano ; Rossini, Paolo Maria ; Tecchio, Franca</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6088-185dacb12ac6fe3a97cc39f84af7e035c71ad7e0f4d2d7e75893837905a133aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Algorithms</topic><topic>Ankle</topic><topic>Ankle Joint - physiology</topic><topic>ankle movement</topic><topic>Attention</topic><topic>Biological and medical sciences</topic><topic>Brain Mapping</topic><topic>Cortex (motor)</topic><topic>Cortex (somatosensory)</topic><topic>Electric Stimulation</topic><topic>Electrical stimuli</topic><topic>Electromyography</topic><topic>EMG</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hemispheric laterality</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Limbs</topic><topic>Magnetoencephalography</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Motion Therapy, Continuous Passive</topic><topic>Motor Cortex - physiology</topic><topic>Movement - physiology</topic><topic>Muscle contraction</topic><topic>Muscle Contraction - physiology</topic><topic>Nervous system</topic><topic>Orthotic Devices</topic><topic>peroneal nerve</topic><topic>Pilot Projects</topic><topic>Radiodiagnosis. Nmr imagery. Nmr spectrometry</topic><topic>Rehabilitation</topic><topic>Rhythms</topic><topic>sensorimotor</topic><topic>sensorimotor system</topic><topic>Shade</topic><topic>Somatosensory Cortex - physiology</topic><topic>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</topic><topic>Stroke</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pittaccio, Simone</creatorcontrib><creatorcontrib>Zappasodi, Filippo</creatorcontrib><creatorcontrib>Viscuso, Stefano</creatorcontrib><creatorcontrib>Mastrolilli, Francesca</creatorcontrib><creatorcontrib>Ercolani, Matilde</creatorcontrib><creatorcontrib>Passarelli, Francesco</creatorcontrib><creatorcontrib>Molteni, Franco</creatorcontrib><creatorcontrib>Besseghini, Stefano</creatorcontrib><creatorcontrib>Rossini, Paolo Maria</creatorcontrib><creatorcontrib>Tecchio, Franca</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>PubMed Central (Full Participant titles)</collection><jtitle>Human brain mapping</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pittaccio, Simone</au><au>Zappasodi, Filippo</au><au>Viscuso, Stefano</au><au>Mastrolilli, Francesca</au><au>Ercolani, Matilde</au><au>Passarelli, Francesco</au><au>Molteni, Franco</au><au>Besseghini, Stefano</au><au>Rossini, Paolo Maria</au><au>Tecchio, Franca</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary sensory and motor cortex activities during voluntary and passive ankle mobilization by the SHADE orthosis</atitle><jtitle>Human brain mapping</jtitle><addtitle>Hum. Brain Mapp</addtitle><date>2011-01</date><risdate>2011</risdate><volume>32</volume><issue>1</issue><spage>60</spage><epage>70</epage><pages>60-70</pages><issn>1065-9471</issn><issn>1097-0193</issn><eissn>1097-0193</eissn><abstract>This study investigates cortical involvement during ankle passive mobilization in healthy subjects, and is part of a pilot study on stroke patient rehabilitation. Magnetoencephalographic signals from the primary sensorimotor areas devoted to the lower limb were collected together with simultaneous electromyographic activities from tibialis anterior (TA). This was done bilaterally, on seven healthy subjects (aged 29 ± 7), during rest, left and right passive ankle dorsiflexion (imparted through the SHADE orthosis, O‐PM, or neuromuscular electrical stimulation, NMES‐PM), and during active isometric contraction (IC‐AM). The effects of focussing attention on ankle passive movements were considered. Primary sensory (FSS1) and motor (FSM1) area activities were discriminated by the Functional Source Separation algorithm. Only contralateral FSS1 was recruited by common peroneal nerve stimulation and only contralateral FSM1 displayed coherence with TA muscular activity. FSM1 showed higher power of gamma rhythms (33–90 Hz) than FSS1. Both sources displayed higher beta (14–32 Hz) and gamma powers in the left than in the right hemisphere. Both sources displayed a bilateral reduction of beta power during IC‐AM with respect to rest. Only FSS1 beta band power reduced during O‐PM. No beta band modulation was observed of either source during NMES‐PM. Mutual FSS1‐FSM1 coherence in gamma2 band (61–90 Hz) showed a slight trend towards an increase when focussing attention during O‐PM. Somatosensory and motor counterparts of lower limb cortical representations were discriminated in both hemispheres. SHADE was effective in generating repeatable dorsiflexion and inducing primary sensory involvement similarly to voluntary movement. Hum Brain Mapp, 2010. © 2010 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20336689</pmid><doi>10.1002/hbm.20998</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Algorithms Ankle Ankle Joint - physiology ankle movement Attention Biological and medical sciences Brain Mapping Cortex (motor) Cortex (somatosensory) Electric Stimulation Electrical stimuli Electromyography EMG Female Fundamental and applied biological sciences. Psychology Hemispheric laterality Humans Investigative techniques, diagnostic techniques (general aspects) Limbs Magnetoencephalography Male Medical sciences Motion Therapy, Continuous Passive Motor Cortex - physiology Movement - physiology Muscle contraction Muscle Contraction - physiology Nervous system Orthotic Devices peroneal nerve Pilot Projects Radiodiagnosis. Nmr imagery. Nmr spectrometry Rehabilitation Rhythms sensorimotor sensorimotor system Shade Somatosensory Cortex - physiology Somesthesis and somesthetic pathways (proprioception, exteroception, nociception) interoception electrolocation. Sensory receptors Stroke Vertebrates: nervous system and sense organs |
title | Primary sensory and motor cortex activities during voluntary and passive ankle mobilization by the SHADE orthosis |
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