Transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleus

The cochlear nucleus (CN) is the first site of multisensory integration in the ascending auditory pathway. The principal output neurons of the dorsal cochlear nucleus (DCN), fusiform cells, receive somatosensory information relayed by the CN granule cells from the trigeminal and dorsal column pathwa...

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Main Authors: Calvin eWu, David T. Martel, Susan eShore
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-08-01
Series:Frontiers in Systems Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnsys.2015.00116/full
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spelling doaj-a9d2be19d7b6441e87404924d10b20802020-11-24T22:38:02ZengFrontiers Media S.A.Frontiers in Systems Neuroscience1662-51372015-08-01910.3389/fnsys.2015.00116158651Transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleusCalvin eWu0David T. Martel1Susan eShore2University of MichiganUniversity of MichiganUniversity of MichiganThe cochlear nucleus (CN) is the first site of multisensory integration in the ascending auditory pathway. The principal output neurons of the dorsal cochlear nucleus (DCN), fusiform cells, receive somatosensory information relayed by the CN granule cells from the trigeminal and dorsal column pathways. Integration of somatosensory and auditory inputs results in long-term enhancement or suppression in a stimulus timing dependent manner. Here we demonstrate that stimulus timing dependent plasticity (STDP) can be induced in DCN fusiform cells using paired auditory and transcutaneous electrical stimulation of the face and neck to activate trigeminal and dorsal column pathways to the CN, respectively. Long-lasting changes in fusiform cell firing rates persisted for up to two hours after this bimodal stimulation, and followed Hebbian or anti-Hebbian rules, depending on tone duration, but not somatosensory stimulation location: 50 ms paired tones evoked predominantly Hebbian, while 10 ms paired tones evoked predominantly anti-Hebbian plasticity. The tone-duration dependent STDP was strongly correlated with first inter-spike intervals, implicating intrinsic cellular properties as determinants of STDP. This study demonstrates that transcutaneous stimulation with precise auditory-somatosensory timing parameters can non-invasively induce fusiform cell long-term modulation, which could be harnessed in the future to moderate tinnitus-related hyperactivity in DCN.http://journal.frontiersin.org/Journal/10.3389/fnsys.2015.00116/fullTinnitusTranscutaneous Electric Nerve Stimulationmultisensory integrationdorsal cochlear nucleusHebbian plasticitystimulus timing dependent plasticity
collection DOAJ
language English
format Article
sources DOAJ
author Calvin eWu
David T. Martel
Susan eShore
spellingShingle Calvin eWu
David T. Martel
Susan eShore
Transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleus
Frontiers in Systems Neuroscience
Tinnitus
Transcutaneous Electric Nerve Stimulation
multisensory integration
dorsal cochlear nucleus
Hebbian plasticity
stimulus timing dependent plasticity
author_facet Calvin eWu
David T. Martel
Susan eShore
author_sort Calvin eWu
title Transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleus
title_short Transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleus
title_full Transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleus
title_fullStr Transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleus
title_full_unstemmed Transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleus
title_sort transcutaneous induction of stimulus timing dependent plasticity in dorsal cochlear nucleus
publisher Frontiers Media S.A.
series Frontiers in Systems Neuroscience
issn 1662-5137
publishDate 2015-08-01
description The cochlear nucleus (CN) is the first site of multisensory integration in the ascending auditory pathway. The principal output neurons of the dorsal cochlear nucleus (DCN), fusiform cells, receive somatosensory information relayed by the CN granule cells from the trigeminal and dorsal column pathways. Integration of somatosensory and auditory inputs results in long-term enhancement or suppression in a stimulus timing dependent manner. Here we demonstrate that stimulus timing dependent plasticity (STDP) can be induced in DCN fusiform cells using paired auditory and transcutaneous electrical stimulation of the face and neck to activate trigeminal and dorsal column pathways to the CN, respectively. Long-lasting changes in fusiform cell firing rates persisted for up to two hours after this bimodal stimulation, and followed Hebbian or anti-Hebbian rules, depending on tone duration, but not somatosensory stimulation location: 50 ms paired tones evoked predominantly Hebbian, while 10 ms paired tones evoked predominantly anti-Hebbian plasticity. The tone-duration dependent STDP was strongly correlated with first inter-spike intervals, implicating intrinsic cellular properties as determinants of STDP. This study demonstrates that transcutaneous stimulation with precise auditory-somatosensory timing parameters can non-invasively induce fusiform cell long-term modulation, which could be harnessed in the future to moderate tinnitus-related hyperactivity in DCN.
topic Tinnitus
Transcutaneous Electric Nerve Stimulation
multisensory integration
dorsal cochlear nucleus
Hebbian plasticity
stimulus timing dependent plasticity
url http://journal.frontiersin.org/Journal/10.3389/fnsys.2015.00116/full
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AT davidtmartel transcutaneousinductionofstimulustimingdependentplasticityindorsalcochlearnucleus
AT susaneshore transcutaneousinductionofstimulustimingdependentplasticityindorsalcochlearnucleus
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