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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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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. |
format | Online Article Text |
id | pubmed-6635381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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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