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Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia

Chronic pain presents a major unmet clinical problem. The development of more effective treatments is hindered by our limited understanding of the neuronal circuits underlying sensory perception. Here, we show that parvalbumin (PV)-expressing dorsal horn interneurons modulate the passage of sensory...

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Autores principales: Boyle, Kieran A., Gradwell, Mark A., Yasaka, Toshiharu, Dickie, Allen C., Polgár, Erika, Ganley, Robert P., Orr, Desmond P.H., Watanabe, Masahiko, Abraira, Victoria E., Kuehn, Emily D., Zimmerman, Amanda L., Ginty, David D., Callister, Robert J., Graham, Brett A., Hughes, David I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635381/
https://www.ncbi.nlm.nih.gov/pubmed/31291586
http://dx.doi.org/10.1016/j.celrep.2019.06.040
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author Boyle, Kieran A.
Gradwell, Mark A.
Yasaka, Toshiharu
Dickie, Allen C.
Polgár, Erika
Ganley, Robert P.
Orr, Desmond P.H.
Watanabe, Masahiko
Abraira, Victoria E.
Kuehn, Emily D.
Zimmerman, Amanda L.
Ginty, David D.
Callister, Robert J.
Graham, Brett A.
Hughes, David I.
author_facet Boyle, Kieran A.
Gradwell, Mark A.
Yasaka, Toshiharu
Dickie, Allen C.
Polgár, Erika
Ganley, Robert P.
Orr, Desmond P.H.
Watanabe, Masahiko
Abraira, Victoria E.
Kuehn, Emily D.
Zimmerman, Amanda L.
Ginty, David D.
Callister, Robert J.
Graham, Brett A.
Hughes, David I.
author_sort Boyle, Kieran A.
collection PubMed
description Chronic pain presents a major unmet clinical problem. The development of more effective treatments is hindered by our limited understanding of the neuronal circuits underlying sensory perception. Here, we show that parvalbumin (PV)-expressing dorsal horn interneurons modulate the passage of sensory information conveyed by low-threshold mechanoreceptors (LTMRs) directly via presynaptic inhibition and also gate the polysynaptic relay of LTMR input to pain circuits by inhibiting lamina II excitatory interneurons whose axons project into lamina I. We show changes in the functional properties of these PV interneurons following peripheral nerve injury and that silencing these cells unmasks a circuit that allows innocuous touch inputs to activate pain circuits by increasing network activity in laminae I–IV. Such changes are likely to result in the development of tactile allodynia and could be targeted for more effective treatment of mechanical pain.
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spelling pubmed-66353812019-07-25 Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia Boyle, Kieran A. Gradwell, Mark A. Yasaka, Toshiharu Dickie, Allen C. Polgár, Erika Ganley, Robert P. Orr, Desmond P.H. Watanabe, Masahiko Abraira, Victoria E. Kuehn, Emily D. Zimmerman, Amanda L. Ginty, David D. Callister, Robert J. Graham, Brett A. Hughes, David I. Cell Rep Article Chronic pain presents a major unmet clinical problem. The development of more effective treatments is hindered by our limited understanding of the neuronal circuits underlying sensory perception. Here, we show that parvalbumin (PV)-expressing dorsal horn interneurons modulate the passage of sensory information conveyed by low-threshold mechanoreceptors (LTMRs) directly via presynaptic inhibition and also gate the polysynaptic relay of LTMR input to pain circuits by inhibiting lamina II excitatory interneurons whose axons project into lamina I. We show changes in the functional properties of these PV interneurons following peripheral nerve injury and that silencing these cells unmasks a circuit that allows innocuous touch inputs to activate pain circuits by increasing network activity in laminae I–IV. Such changes are likely to result in the development of tactile allodynia and could be targeted for more effective treatment of mechanical pain. Cell Press 2019-07-09 /pmc/articles/PMC6635381/ /pubmed/31291586 http://dx.doi.org/10.1016/j.celrep.2019.06.040 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Boyle, Kieran A.
Gradwell, Mark A.
Yasaka, Toshiharu
Dickie, Allen C.
Polgár, Erika
Ganley, Robert P.
Orr, Desmond P.H.
Watanabe, Masahiko
Abraira, Victoria E.
Kuehn, Emily D.
Zimmerman, Amanda L.
Ginty, David D.
Callister, Robert J.
Graham, Brett A.
Hughes, David I.
Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia
title Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia
title_full Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia
title_fullStr Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia
title_full_unstemmed Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia
title_short Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia
title_sort defining a spinal microcircuit that gates myelinated afferent input: implications for tactile allodynia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635381/
https://www.ncbi.nlm.nih.gov/pubmed/31291586
http://dx.doi.org/10.1016/j.celrep.2019.06.040
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