Cargando…

Distal Electroacupuncture at the LI4 Acupoint Reduces CFA-Induced Inflammatory Pain via the Brain TRPV1 Signaling Pathway

There is accumulating evidence supporting electroacupuncture’s (EA) therapeutic effects. In mice, local EA reliably attenuates inflammatory pain and increases the transient receptor potential cation channel, subfamily V, member 1 (TRPV1). However, the effect of distal acupoint EA on pain control has...

Descripción completa

Detalles Bibliográficos
Autores principales: Yen, Chia-Ming, Wu, Tong-Chien, Hsieh, Ching-Liang, Huang, Yu-Wei, Lin, Yi-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769885/
https://www.ncbi.nlm.nih.gov/pubmed/31510092
http://dx.doi.org/10.3390/ijms20184471
_version_ 1783455341711720448
author Yen, Chia-Ming
Wu, Tong-Chien
Hsieh, Ching-Liang
Huang, Yu-Wei
Lin, Yi-Wen
author_facet Yen, Chia-Ming
Wu, Tong-Chien
Hsieh, Ching-Liang
Huang, Yu-Wei
Lin, Yi-Wen
author_sort Yen, Chia-Ming
collection PubMed
description There is accumulating evidence supporting electroacupuncture’s (EA) therapeutic effects. In mice, local EA reliably attenuates inflammatory pain and increases the transient receptor potential cation channel, subfamily V, member 1 (TRPV1). However, the effect of distal acupoint EA on pain control has rarely been studied. We used a mouse model to investigate the analgesic effect of distal EA by measuring TRPV1 expression in the brain. Complete Freund’s adjuvant (CFA) was injected into mice’s hind paws to induce inflammatory pain. The EA-treated group received EA at the LI4 acupoint on the bilateral forefeet on the second and the third days, whereas the control group underwent sham manipulation. Mechanical and thermal pain behavior tests showed that the EA-treated group experienced inflammatory pain alleviation immediately after EA, which did not occur in the sham group. Additionally, following CFA injection, the expression of TRPV1-associated molecules such as phosphorylated protein kinase A (pPKA), extracelluar signal-regulated kinase (pERK), and cAMP-response-element-binding protein (pCREB) increased in the prefrontal cortex (PFC) and the hypothalamus but decreased in the periaqueductal gray (PAG) area. These changes were significantly attenuated by EA but not sham EA. Our results show an analgesic effect of distal EA, which is based on the traditional Chinese medicine theory. The mechanism underlying this analgesic effect involves TRPV1 in the PFC, the hypothalamus, and the PAG. These novel findings are relevant for the evaluation and the treatment of clinical inflammatory pain syndrome.
format Online
Article
Text
id pubmed-6769885
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-67698852019-10-30 Distal Electroacupuncture at the LI4 Acupoint Reduces CFA-Induced Inflammatory Pain via the Brain TRPV1 Signaling Pathway Yen, Chia-Ming Wu, Tong-Chien Hsieh, Ching-Liang Huang, Yu-Wei Lin, Yi-Wen Int J Mol Sci Article There is accumulating evidence supporting electroacupuncture’s (EA) therapeutic effects. In mice, local EA reliably attenuates inflammatory pain and increases the transient receptor potential cation channel, subfamily V, member 1 (TRPV1). However, the effect of distal acupoint EA on pain control has rarely been studied. We used a mouse model to investigate the analgesic effect of distal EA by measuring TRPV1 expression in the brain. Complete Freund’s adjuvant (CFA) was injected into mice’s hind paws to induce inflammatory pain. The EA-treated group received EA at the LI4 acupoint on the bilateral forefeet on the second and the third days, whereas the control group underwent sham manipulation. Mechanical and thermal pain behavior tests showed that the EA-treated group experienced inflammatory pain alleviation immediately after EA, which did not occur in the sham group. Additionally, following CFA injection, the expression of TRPV1-associated molecules such as phosphorylated protein kinase A (pPKA), extracelluar signal-regulated kinase (pERK), and cAMP-response-element-binding protein (pCREB) increased in the prefrontal cortex (PFC) and the hypothalamus but decreased in the periaqueductal gray (PAG) area. These changes were significantly attenuated by EA but not sham EA. Our results show an analgesic effect of distal EA, which is based on the traditional Chinese medicine theory. The mechanism underlying this analgesic effect involves TRPV1 in the PFC, the hypothalamus, and the PAG. These novel findings are relevant for the evaluation and the treatment of clinical inflammatory pain syndrome. MDPI 2019-09-10 /pmc/articles/PMC6769885/ /pubmed/31510092 http://dx.doi.org/10.3390/ijms20184471 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yen, Chia-Ming
Wu, Tong-Chien
Hsieh, Ching-Liang
Huang, Yu-Wei
Lin, Yi-Wen
Distal Electroacupuncture at the LI4 Acupoint Reduces CFA-Induced Inflammatory Pain via the Brain TRPV1 Signaling Pathway
title Distal Electroacupuncture at the LI4 Acupoint Reduces CFA-Induced Inflammatory Pain via the Brain TRPV1 Signaling Pathway
title_full Distal Electroacupuncture at the LI4 Acupoint Reduces CFA-Induced Inflammatory Pain via the Brain TRPV1 Signaling Pathway
title_fullStr Distal Electroacupuncture at the LI4 Acupoint Reduces CFA-Induced Inflammatory Pain via the Brain TRPV1 Signaling Pathway
title_full_unstemmed Distal Electroacupuncture at the LI4 Acupoint Reduces CFA-Induced Inflammatory Pain via the Brain TRPV1 Signaling Pathway
title_short Distal Electroacupuncture at the LI4 Acupoint Reduces CFA-Induced Inflammatory Pain via the Brain TRPV1 Signaling Pathway
title_sort distal electroacupuncture at the li4 acupoint reduces cfa-induced inflammatory pain via the brain trpv1 signaling pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769885/
https://www.ncbi.nlm.nih.gov/pubmed/31510092
http://dx.doi.org/10.3390/ijms20184471
work_keys_str_mv AT yenchiaming distalelectroacupunctureattheli4acupointreducescfainducedinflammatorypainviathebraintrpv1signalingpathway
AT wutongchien distalelectroacupunctureattheli4acupointreducescfainducedinflammatorypainviathebraintrpv1signalingpathway
AT hsiehchingliang distalelectroacupunctureattheli4acupointreducescfainducedinflammatorypainviathebraintrpv1signalingpathway
AT huangyuwei distalelectroacupunctureattheli4acupointreducescfainducedinflammatorypainviathebraintrpv1signalingpathway
AT linyiwen distalelectroacupunctureattheli4acupointreducescfainducedinflammatorypainviathebraintrpv1signalingpathway