Transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.

Scratching relieves itch, but the underlying neural mechanisms are poorly understood. We presently investigated a role for the inhibitory neurotransmitters GABA and glycine in scratch-evoked inhibition of spinal itch-signaling neurons in a mouse model of chronic dry skin itch. Superficial dorsal hor...

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Main Authors: Tasuku Akiyama, Mirela Iodi Carstens, Earl Carstens
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3144926?pdf=render
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spelling doaj-f95c0d1d4c9844c5a02a4260104a168a2020-11-25T01:50:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0167e2266510.1371/journal.pone.0022665Transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.Tasuku AkiyamaMirela Iodi CarstensEarl CarstensScratching relieves itch, but the underlying neural mechanisms are poorly understood. We presently investigated a role for the inhibitory neurotransmitters GABA and glycine in scratch-evoked inhibition of spinal itch-signaling neurons in a mouse model of chronic dry skin itch. Superficial dorsal horn neurons ipsilateral to hindpaw dry skin treatment exhibited a high level of spontaneous firing that was significantly attenuated by cutaneous scratching, pinch and noxious heat. Scratch-evoked inhibition was nearly abolished by spinal delivery of the glycine antagonist, strychnine, and was markedly attenuated by respective GABA(A) and GABA(B) antagonists bicuculline and saclofen. Scratch-evoked inhibition was also significantly attenuated (but not abolished) by interruption of the upper cervical spinal cord, indicating the involvement of both segmental and suprasegmental circuits that engage glycine- and GABA-mediated inhibition of spinal itch-signaling neurons by noxious counterstimuli.http://europepmc.org/articles/PMC3144926?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Tasuku Akiyama
Mirela Iodi Carstens
Earl Carstens
spellingShingle Tasuku Akiyama
Mirela Iodi Carstens
Earl Carstens
Transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.
PLoS ONE
author_facet Tasuku Akiyama
Mirela Iodi Carstens
Earl Carstens
author_sort Tasuku Akiyama
title Transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.
title_short Transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.
title_full Transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.
title_fullStr Transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.
title_full_unstemmed Transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.
title_sort transmitters and pathways mediating inhibition of spinal itch-signaling neurons by scratching and other counterstimuli.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Scratching relieves itch, but the underlying neural mechanisms are poorly understood. We presently investigated a role for the inhibitory neurotransmitters GABA and glycine in scratch-evoked inhibition of spinal itch-signaling neurons in a mouse model of chronic dry skin itch. Superficial dorsal horn neurons ipsilateral to hindpaw dry skin treatment exhibited a high level of spontaneous firing that was significantly attenuated by cutaneous scratching, pinch and noxious heat. Scratch-evoked inhibition was nearly abolished by spinal delivery of the glycine antagonist, strychnine, and was markedly attenuated by respective GABA(A) and GABA(B) antagonists bicuculline and saclofen. Scratch-evoked inhibition was also significantly attenuated (but not abolished) by interruption of the upper cervical spinal cord, indicating the involvement of both segmental and suprasegmental circuits that engage glycine- and GABA-mediated inhibition of spinal itch-signaling neurons by noxious counterstimuli.
url http://europepmc.org/articles/PMC3144926?pdf=render
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AT earlcarstens transmittersandpathwaysmediatinginhibitionofspinalitchsignalingneuronsbyscratchingandothercounterstimuli
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