Shared nociceptive dorsal root ganglion neurons participating in acupoint sensitization

When the body is under pathological stress (injury or disease), the status of associated acupoints changes, including decreased pain threshold. Such changes in acupoint from a “silent” to an “active” state are considered “acupoint sensitization,” which has become an important indicator of acupoint s...

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Main Authors: Wanrong Li, Jia Liu, Aiwen Chen, Danqing Dai, Tiantian Zhao, Qiong Liu, Jianren Song, Lize Xiong, Xiao-Fei Gao
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Molecular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnmol.2022.974007/full
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author Wanrong Li
Wanrong Li
Wanrong Li
Wanrong Li
Jia Liu
Aiwen Chen
Aiwen Chen
Aiwen Chen
Aiwen Chen
Danqing Dai
Danqing Dai
Danqing Dai
Danqing Dai
Tiantian Zhao
Tiantian Zhao
Tiantian Zhao
Tiantian Zhao
Qiong Liu
Qiong Liu
Qiong Liu
Qiong Liu
Jianren Song
Lize Xiong
Lize Xiong
Lize Xiong
Lize Xiong
Xiao-Fei Gao
Xiao-Fei Gao
Xiao-Fei Gao
Xiao-Fei Gao
author_facet Wanrong Li
Wanrong Li
Wanrong Li
Wanrong Li
Jia Liu
Aiwen Chen
Aiwen Chen
Aiwen Chen
Aiwen Chen
Danqing Dai
Danqing Dai
Danqing Dai
Danqing Dai
Tiantian Zhao
Tiantian Zhao
Tiantian Zhao
Tiantian Zhao
Qiong Liu
Qiong Liu
Qiong Liu
Qiong Liu
Jianren Song
Lize Xiong
Lize Xiong
Lize Xiong
Lize Xiong
Xiao-Fei Gao
Xiao-Fei Gao
Xiao-Fei Gao
Xiao-Fei Gao
author_sort Wanrong Li
collection DOAJ
description When the body is under pathological stress (injury or disease), the status of associated acupoints changes, including decreased pain threshold. Such changes in acupoint from a “silent” to an “active” state are considered “acupoint sensitization,” which has become an important indicator of acupoint selection. However, the mechanism of acupoint sensitization remains unclear. In this study, by retrograde tracing, morphological, chemogenetic, and behavioral methods, we found there are some dorsal root ganglion (DRG) neurons innervating the ST36 acupoint and ipsilateral hind paw (IHP) plantar simultaneously. Inhibition of these shared neurons induced analgesia in the complete Freund’s adjuvant (CFA) pain model and obstruction of nociceptive sensation in normal mice, and elevated the mechanical pain threshold (MPT) of ST36 acupoint in the CFA model. Excitation of shared neurons induced pain and declined the MPT of ST36 acupoint. Furthermore, most of the shared DRG neurons express TRPV1, a marker of nociceptive neurons. These results indicate that the shared nociceptive DRG neurons participate in ST36 acupoint sensitization in CFA-induced chronic pain. This raised a neural mechanism of acupoint sensitization at the level of primary sensory transmission.
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spelling doaj.art-61218481efd4458d8f5c7e45df2f48ad2022-12-22T01:35:59ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992022-08-011510.3389/fnmol.2022.974007974007Shared nociceptive dorsal root ganglion neurons participating in acupoint sensitizationWanrong Li0Wanrong Li1Wanrong Li2Wanrong Li3Jia Liu4Aiwen Chen5Aiwen Chen6Aiwen Chen7Aiwen Chen8Danqing Dai9Danqing Dai10Danqing Dai11Danqing Dai12Tiantian Zhao13Tiantian Zhao14Tiantian Zhao15Tiantian Zhao16Qiong Liu17Qiong Liu18Qiong Liu19Qiong Liu20Jianren Song21Lize Xiong22Lize Xiong23Lize Xiong24Lize Xiong25Xiao-Fei Gao26Xiao-Fei Gao27Xiao-Fei Gao28Xiao-Fei Gao29Translational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaClinical Research Center for Anesthesiology and Perioperative Medicine, Tongji University, Shanghai, ChinaDepartment of Anesthesiology and Perioperative Medicine, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaShanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Shanghai, ChinaFaculty of Anesthesiology, Changhai Hospital, Naval Medical University, Shanghai, ChinaTranslational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaClinical Research Center for Anesthesiology and Perioperative Medicine, Tongji University, Shanghai, ChinaDepartment of Anesthesiology and Perioperative Medicine, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaShanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Shanghai, ChinaTranslational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaClinical Research Center for Anesthesiology and Perioperative Medicine, Tongji University, Shanghai, ChinaDepartment of Anesthesiology and Perioperative Medicine, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaShanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Shanghai, ChinaTranslational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaClinical Research Center for Anesthesiology and Perioperative Medicine, Tongji University, Shanghai, ChinaDepartment of Anesthesiology and Perioperative Medicine, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaShanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Shanghai, ChinaTranslational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaClinical Research Center for Anesthesiology and Perioperative Medicine, Tongji University, Shanghai, ChinaDepartment of Anesthesiology and Perioperative Medicine, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaShanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Shanghai, ChinaTranslational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaTranslational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaClinical Research Center for Anesthesiology and Perioperative Medicine, Tongji University, Shanghai, ChinaDepartment of Anesthesiology and Perioperative Medicine, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaShanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Shanghai, ChinaTranslational Research Institute of Brain and Brain-Like Intelligence, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaClinical Research Center for Anesthesiology and Perioperative Medicine, Tongji University, Shanghai, ChinaDepartment of Anesthesiology and Perioperative Medicine, Shanghai Fourth People’s Hospital, School of Medicine, Tongji University, Shanghai, ChinaShanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Shanghai, ChinaWhen the body is under pathological stress (injury or disease), the status of associated acupoints changes, including decreased pain threshold. Such changes in acupoint from a “silent” to an “active” state are considered “acupoint sensitization,” which has become an important indicator of acupoint selection. However, the mechanism of acupoint sensitization remains unclear. In this study, by retrograde tracing, morphological, chemogenetic, and behavioral methods, we found there are some dorsal root ganglion (DRG) neurons innervating the ST36 acupoint and ipsilateral hind paw (IHP) plantar simultaneously. Inhibition of these shared neurons induced analgesia in the complete Freund’s adjuvant (CFA) pain model and obstruction of nociceptive sensation in normal mice, and elevated the mechanical pain threshold (MPT) of ST36 acupoint in the CFA model. Excitation of shared neurons induced pain and declined the MPT of ST36 acupoint. Furthermore, most of the shared DRG neurons express TRPV1, a marker of nociceptive neurons. These results indicate that the shared nociceptive DRG neurons participate in ST36 acupoint sensitization in CFA-induced chronic pain. This raised a neural mechanism of acupoint sensitization at the level of primary sensory transmission.https://www.frontiersin.org/articles/10.3389/fnmol.2022.974007/fullpaindorsal root ganglionacupoint sensitizationST36 acupointnociceptive neuronacupuncture
spellingShingle Wanrong Li
Wanrong Li
Wanrong Li
Wanrong Li
Jia Liu
Aiwen Chen
Aiwen Chen
Aiwen Chen
Aiwen Chen
Danqing Dai
Danqing Dai
Danqing Dai
Danqing Dai
Tiantian Zhao
Tiantian Zhao
Tiantian Zhao
Tiantian Zhao
Qiong Liu
Qiong Liu
Qiong Liu
Qiong Liu
Jianren Song
Lize Xiong
Lize Xiong
Lize Xiong
Lize Xiong
Xiao-Fei Gao
Xiao-Fei Gao
Xiao-Fei Gao
Xiao-Fei Gao
Shared nociceptive dorsal root ganglion neurons participating in acupoint sensitization
Frontiers in Molecular Neuroscience
pain
dorsal root ganglion
acupoint sensitization
ST36 acupoint
nociceptive neuron
acupuncture
title Shared nociceptive dorsal root ganglion neurons participating in acupoint sensitization
title_full Shared nociceptive dorsal root ganglion neurons participating in acupoint sensitization
title_fullStr Shared nociceptive dorsal root ganglion neurons participating in acupoint sensitization
title_full_unstemmed Shared nociceptive dorsal root ganglion neurons participating in acupoint sensitization
title_short Shared nociceptive dorsal root ganglion neurons participating in acupoint sensitization
title_sort shared nociceptive dorsal root ganglion neurons participating in acupoint sensitization
topic pain
dorsal root ganglion
acupoint sensitization
ST36 acupoint
nociceptive neuron
acupuncture
url https://www.frontiersin.org/articles/10.3389/fnmol.2022.974007/full
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