Short-latency afferent inhibition modulation during finger movement
When somatosensory input via electrical stimulation of a peripheral nerve precedes a transcranial magnetic stimulation (TMS) pulse over the primary motor cortex (M1) the corticospinal output is substantially reduced, a phenomenon known as short-latency afferent inhibition (SAI). The present study in...
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description | When somatosensory input via electrical stimulation of a peripheral nerve precedes a transcranial magnetic stimulation (TMS) pulse over the primary motor cortex (M1) the corticospinal output is substantially reduced, a phenomenon known as short-latency afferent inhibition (SAI). The present study investigated SAI during rest and during pre-movement, phasic and tonic components of movement. Participants were required to perform an index finger flexion reaction time task in response to an auditory cue. In a series of experiments, SAI was evoked from the mixed, median nerve at the wrist or the cutaneous, digital nerve stimulation of the index finger. To assess the spinal versus cortical origin of movement-related modulation of SAI, F-wave amplitudes were measured during rest and the three movement components. Results indicated that SAI was reduced during all movement components compared to rest, an effect that occurred for both nerves stimulated. Pre-movement SAI reduction was primarily attributed to reduced cortical inhibition, while increased spinal excitability additionally contributed to reduced SAI during tonic and phasic components of movement. SAI was differentially modulated across movement components with mixed but not cutaneous nerve stimulation. These findings reveal that SAI is reduced during movement and this reduction begins as early as the preparation to move. Further, these data suggest that the degree of SAI reduction during movement may be specific to the volume and/or composition of afferent input carried by each nerve. |
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Chacron, Maurice</contributor><creatorcontrib>Asmussen, Michael J ; Jacobs, Mark F ; Lee, Kevin G H ; Zapallow, Christopher M ; Nelson, Aimee J ; J. Chacron, Maurice</creatorcontrib><description>When somatosensory input via electrical stimulation of a peripheral nerve precedes a transcranial magnetic stimulation (TMS) pulse over the primary motor cortex (M1) the corticospinal output is substantially reduced, a phenomenon known as short-latency afferent inhibition (SAI). The present study investigated SAI during rest and during pre-movement, phasic and tonic components of movement. Participants were required to perform an index finger flexion reaction time task in response to an auditory cue. In a series of experiments, SAI was evoked from the mixed, median nerve at the wrist or the cutaneous, digital nerve stimulation of the index finger. To assess the spinal versus cortical origin of movement-related modulation of SAI, F-wave amplitudes were measured during rest and the three movement components. Results indicated that SAI was reduced during all movement components compared to rest, an effect that occurred for both nerves stimulated. Pre-movement SAI reduction was primarily attributed to reduced cortical inhibition, while increased spinal excitability additionally contributed to reduced SAI during tonic and phasic components of movement. SAI was differentially modulated across movement components with mixed but not cutaneous nerve stimulation. These findings reveal that SAI is reduced during movement and this reduction begins as early as the preparation to move. Further, these data suggest that the degree of SAI reduction during movement may be specific to the volume and/or composition of afferent input carried by each nerve.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0060496</identifier><identifier>PMID: 23593228</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Afferent Pathways ; Biology ; Cortex ; Cortex (auditory) ; Cortex (motor) ; Cortex (somatosensory) ; Electric Stimulation ; Electrical stimuli ; Electromyography ; Evoked Potentials, Motor - physiology ; Excitability ; Female ; Finger ; Fingers - physiology ; Human mechanics ; Humans ; Inhibition ; Kinesiology ; Latency ; Locomotion - physiology ; Magnetic brain stimulation ; Magnetic fields ; Male ; Median nerve ; Median Nerve - physiology ; Medicine ; Modulation ; Motor cortex ; Motor Cortex - physiology ; Muscle function ; Parkinson's disease ; Parkinsons disease ; Peripheral nerves ; Peripheral Nerves - physiology ; Physiological aspects ; Pyramidal tracts ; Reaction time ; Reaction time task ; Reduction ; Rest ; Sensory neurons ; Somatosensory cortex ; Transcranial Magnetic Stimulation ; Wrist ; Young Adult</subject><ispartof>PloS one, 2013-04, Vol.8 (4), p.e60496-e60496</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Asmussen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Asmussen et al 2013 Asmussen et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-32d806ea301d400f11a0322f89232f262b7fd1e20364d077d77ad96e6f9424b43</citedby><cites>FETCH-LOGICAL-c692t-32d806ea301d400f11a0322f89232f262b7fd1e20364d077d77ad96e6f9424b43</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/PMC3617156/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617156/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,2098,2917,23849,27907,27908,53774,53776,79351,79352</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23593228$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>J. Chacron, Maurice</contributor><creatorcontrib>Asmussen, Michael J</creatorcontrib><creatorcontrib>Jacobs, Mark F</creatorcontrib><creatorcontrib>Lee, Kevin G H</creatorcontrib><creatorcontrib>Zapallow, Christopher M</creatorcontrib><creatorcontrib>Nelson, Aimee J</creatorcontrib><title>Short-latency afferent inhibition modulation during finger movement</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>When somatosensory input via electrical stimulation of a peripheral nerve precedes a transcranial magnetic stimulation (TMS) pulse over the primary motor cortex (M1) the corticospinal output is substantially reduced, a phenomenon known as short-latency afferent inhibition (SAI). The present study investigated SAI during rest and during pre-movement, phasic and tonic components of movement. Participants were required to perform an index finger flexion reaction time task in response to an auditory cue. In a series of experiments, SAI was evoked from the mixed, median nerve at the wrist or the cutaneous, digital nerve stimulation of the index finger. To assess the spinal versus cortical origin of movement-related modulation of SAI, F-wave amplitudes were measured during rest and the three movement components. Results indicated that SAI was reduced during all movement components compared to rest, an effect that occurred for both nerves stimulated. Pre-movement SAI reduction was primarily attributed to reduced cortical inhibition, while increased spinal excitability additionally contributed to reduced SAI during tonic and phasic components of movement. SAI was differentially modulated across movement components with mixed but not cutaneous nerve stimulation. These findings reveal that SAI is reduced during movement and this reduction begins as early as the preparation to move. Further, these data suggest that the degree of SAI reduction during movement may be specific to the volume and/or composition of afferent input carried by each nerve.</description><subject>Adult</subject><subject>Afferent Pathways</subject><subject>Biology</subject><subject>Cortex</subject><subject>Cortex (auditory)</subject><subject>Cortex (motor)</subject><subject>Cortex (somatosensory)</subject><subject>Electric Stimulation</subject><subject>Electrical stimuli</subject><subject>Electromyography</subject><subject>Evoked Potentials, Motor - physiology</subject><subject>Excitability</subject><subject>Female</subject><subject>Finger</subject><subject>Fingers - physiology</subject><subject>Human mechanics</subject><subject>Humans</subject><subject>Inhibition</subject><subject>Kinesiology</subject><subject>Latency</subject><subject>Locomotion - physiology</subject><subject>Magnetic brain stimulation</subject><subject>Magnetic fields</subject><subject>Male</subject><subject>Median nerve</subject><subject>Median Nerve - 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Chacron, Maurice</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Short-latency afferent inhibition modulation during finger movement</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-04-04</date><risdate>2013</risdate><volume>8</volume><issue>4</issue><spage>e60496</spage><epage>e60496</epage><pages>e60496-e60496</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>When somatosensory input via electrical stimulation of a peripheral nerve precedes a transcranial magnetic stimulation (TMS) pulse over the primary motor cortex (M1) the corticospinal output is substantially reduced, a phenomenon known as short-latency afferent inhibition (SAI). The present study investigated SAI during rest and during pre-movement, phasic and tonic components of movement. Participants were required to perform an index finger flexion reaction time task in response to an auditory cue. In a series of experiments, SAI was evoked from the mixed, median nerve at the wrist or the cutaneous, digital nerve stimulation of the index finger. To assess the spinal versus cortical origin of movement-related modulation of SAI, F-wave amplitudes were measured during rest and the three movement components. Results indicated that SAI was reduced during all movement components compared to rest, an effect that occurred for both nerves stimulated. Pre-movement SAI reduction was primarily attributed to reduced cortical inhibition, while increased spinal excitability additionally contributed to reduced SAI during tonic and phasic components of movement. SAI was differentially modulated across movement components with mixed but not cutaneous nerve stimulation. These findings reveal that SAI is reduced during movement and this reduction begins as early as the preparation to move. Further, these data suggest that the degree of SAI reduction during movement may be specific to the volume and/or composition of afferent input carried by each nerve.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23593228</pmid><doi>10.1371/journal.pone.0060496</doi><tpages>e60496</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Afferent Pathways Biology Cortex Cortex (auditory) Cortex (motor) Cortex (somatosensory) Electric Stimulation Electrical stimuli Electromyography Evoked Potentials, Motor - physiology Excitability Female Finger Fingers - physiology Human mechanics Humans Inhibition Kinesiology Latency Locomotion - physiology Magnetic brain stimulation Magnetic fields Male Median nerve Median Nerve - physiology Medicine Modulation Motor cortex Motor Cortex - physiology Muscle function Parkinson's disease Parkinsons disease Peripheral nerves Peripheral Nerves - physiology Physiological aspects Pyramidal tracts Reaction time Reaction time task Reduction Rest Sensory neurons Somatosensory cortex Transcranial Magnetic Stimulation Wrist Young Adult |
title | Short-latency afferent inhibition modulation during finger movement |
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