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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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