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Adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy
Injury of peripheral nerves may quickly induce severe pain, but the mechanism remains obscure. We observed a rapid onset of spontaneous pain and evoked pain hypersensitivity after acute transection of the L5 spinal nerve (SNT) in awake rats. The outburst of pain was associated with a rapid developme...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529466/ https://www.ncbi.nlm.nih.gov/pubmed/31113988 http://dx.doi.org/10.1038/s41598-019-44172-9 |
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author | Chen, Zhiyong Wang, Tao Fang, Yehong Luo, Dan Anderson, Michael Huang, Qian He, Shaoqiu Song, Xiaodan Cui, Huan Dong, Xinzhong Xie, Yikuan Guan, Yun Ma, Chao |
author_facet | Chen, Zhiyong Wang, Tao Fang, Yehong Luo, Dan Anderson, Michael Huang, Qian He, Shaoqiu Song, Xiaodan Cui, Huan Dong, Xinzhong Xie, Yikuan Guan, Yun Ma, Chao |
author_sort | Chen, Zhiyong |
collection | PubMed |
description | Injury of peripheral nerves may quickly induce severe pain, but the mechanism remains obscure. We observed a rapid onset of spontaneous pain and evoked pain hypersensitivity after acute transection of the L5 spinal nerve (SNT) in awake rats. The outburst of pain was associated with a rapid development of spontaneous activities and hyperexcitability of nociceptive neurons in the adjacent uninjured L4 dorsal root ganglion (DRG), as revealed by both in vivo electrophysiological recording and high-throughput calcium imaging in vivo. Transection of the L4 dorsal root or intrathecal infusion of aminobutyrate aminotransferase inhibitor attenuated the spontaneous activity, suggesting that retrograde signals from the spinal cord may contribute to the sensitization of L4 DRG neurons after L5 SNT. Electrical stimulation of low-threshold afferents proximal to the axotomized L5 spinal nerve attenuated the spontaneous activities in L4 DRG and pain behavior. These findings suggest that peripheral axotomy may quickly induce hyperexcitability of uninjured nociceptors in the adjacent DRG that drives an outburst of pain. |
format | Online Article Text |
id | pubmed-6529466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65294662019-05-30 Adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy Chen, Zhiyong Wang, Tao Fang, Yehong Luo, Dan Anderson, Michael Huang, Qian He, Shaoqiu Song, Xiaodan Cui, Huan Dong, Xinzhong Xie, Yikuan Guan, Yun Ma, Chao Sci Rep Article Injury of peripheral nerves may quickly induce severe pain, but the mechanism remains obscure. We observed a rapid onset of spontaneous pain and evoked pain hypersensitivity after acute transection of the L5 spinal nerve (SNT) in awake rats. The outburst of pain was associated with a rapid development of spontaneous activities and hyperexcitability of nociceptive neurons in the adjacent uninjured L4 dorsal root ganglion (DRG), as revealed by both in vivo electrophysiological recording and high-throughput calcium imaging in vivo. Transection of the L4 dorsal root or intrathecal infusion of aminobutyrate aminotransferase inhibitor attenuated the spontaneous activity, suggesting that retrograde signals from the spinal cord may contribute to the sensitization of L4 DRG neurons after L5 SNT. Electrical stimulation of low-threshold afferents proximal to the axotomized L5 spinal nerve attenuated the spontaneous activities in L4 DRG and pain behavior. These findings suggest that peripheral axotomy may quickly induce hyperexcitability of uninjured nociceptors in the adjacent DRG that drives an outburst of pain. Nature Publishing Group UK 2019-05-21 /pmc/articles/PMC6529466/ /pubmed/31113988 http://dx.doi.org/10.1038/s41598-019-44172-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Zhiyong Wang, Tao Fang, Yehong Luo, Dan Anderson, Michael Huang, Qian He, Shaoqiu Song, Xiaodan Cui, Huan Dong, Xinzhong Xie, Yikuan Guan, Yun Ma, Chao Adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy |
title | Adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy |
title_full | Adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy |
title_fullStr | Adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy |
title_full_unstemmed | Adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy |
title_short | Adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy |
title_sort | adjacent intact nociceptive neurons drive the acute outburst of pain following peripheral axotomy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529466/ https://www.ncbi.nlm.nih.gov/pubmed/31113988 http://dx.doi.org/10.1038/s41598-019-44172-9 |
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