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Purinergic signaling in microglia in the pathogenesis of neuropathic pain

Nerve injury often causes debilitating chronic pain, referred to as neuropathic pain, which is refractory to currently available analgesics including morphine. Many reports indicate that activated spinal microglia evoke neuropathic pain. The P2X4 receptor (P2X4R), a subtype of ionotropic ATP recepto...

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Autor principal: INOUE, Kazuhide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489427/
https://www.ncbi.nlm.nih.gov/pubmed/28413195
http://dx.doi.org/10.2183/pjab.93.011
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author INOUE, Kazuhide
author_facet INOUE, Kazuhide
author_sort INOUE, Kazuhide
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description Nerve injury often causes debilitating chronic pain, referred to as neuropathic pain, which is refractory to currently available analgesics including morphine. Many reports indicate that activated spinal microglia evoke neuropathic pain. The P2X4 receptor (P2X4R), a subtype of ionotropic ATP receptors, is upregulated in spinal microglia after nerve injury by several factors, including CC chemokine receptor CCR2, the extracellular matrix protein fibronectin in the spinal cord, interferon regulatory factor 8 (IRF8) and IRF5. Inhibition of P2X4R function suppresses neuropathic pain, indicating that microglial P2X4R play a key role in evoking neuropathic pain.
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spelling pubmed-54894272017-08-09 Purinergic signaling in microglia in the pathogenesis of neuropathic pain INOUE, Kazuhide Proc Jpn Acad Ser B Phys Biol Sci Review Nerve injury often causes debilitating chronic pain, referred to as neuropathic pain, which is refractory to currently available analgesics including morphine. Many reports indicate that activated spinal microglia evoke neuropathic pain. The P2X4 receptor (P2X4R), a subtype of ionotropic ATP receptors, is upregulated in spinal microglia after nerve injury by several factors, including CC chemokine receptor CCR2, the extracellular matrix protein fibronectin in the spinal cord, interferon regulatory factor 8 (IRF8) and IRF5. Inhibition of P2X4R function suppresses neuropathic pain, indicating that microglial P2X4R play a key role in evoking neuropathic pain. The Japan Academy 2017-04-11 /pmc/articles/PMC5489427/ /pubmed/28413195 http://dx.doi.org/10.2183/pjab.93.011 Text en © 2017 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
INOUE, Kazuhide
Purinergic signaling in microglia in the pathogenesis of neuropathic pain
title Purinergic signaling in microglia in the pathogenesis of neuropathic pain
title_full Purinergic signaling in microglia in the pathogenesis of neuropathic pain
title_fullStr Purinergic signaling in microglia in the pathogenesis of neuropathic pain
title_full_unstemmed Purinergic signaling in microglia in the pathogenesis of neuropathic pain
title_short Purinergic signaling in microglia in the pathogenesis of neuropathic pain
title_sort purinergic signaling in microglia in the pathogenesis of neuropathic pain
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489427/
https://www.ncbi.nlm.nih.gov/pubmed/28413195
http://dx.doi.org/10.2183/pjab.93.011
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