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Analgesic mechanism of electroacupuncture in a rat L5 spinal nerve ligation model

The aim of this study was to investigate the analgesic mechanism of electroacupuncture (EA) in the treatment of neuropathological pain. A total of 60 Sprague-Dawley rats were randomly divided into three groups, namely the spinal nerve ligation (SNL), electroacupuncture (SNL + EA) and normal control...

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Autores principales: XUE, CHUNCHUN, XIE, LEI, LI, XIA, CAI, JIANFENG, GU, ZHEN, WANG, KAIQIANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316988/
https://www.ncbi.nlm.nih.gov/pubmed/25667665
http://dx.doi.org/10.3892/etm.2015.2165
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author XUE, CHUNCHUN
XIE, LEI
LI, XIA
CAI, JIANFENG
GU, ZHEN
WANG, KAIQIANG
author_facet XUE, CHUNCHUN
XIE, LEI
LI, XIA
CAI, JIANFENG
GU, ZHEN
WANG, KAIQIANG
author_sort XUE, CHUNCHUN
collection PubMed
description The aim of this study was to investigate the analgesic mechanism of electroacupuncture (EA) in the treatment of neuropathological pain. A total of 60 Sprague-Dawley rats were randomly divided into three groups, namely the spinal nerve ligation (SNL), electroacupuncture (SNL + EA) and normal control groups, with 20 rats in each group. The up-down method was used to determine the bipedal 50% mechanical paw withdrawal threshold (PWT). The ultrastructure of the injured-side L5 nerve root (n=6) was observed by electron microscopy. The mRNA levels of brain-derived neurotrophic factor (BDNF) and purinergic receptor P2X, ligand-gated ion channel 4 (P2X4) in the spinal cord (n=14) were determined by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The postoperative PWT of the injured-side hindpaw in the SNL group at each time point was lower than that in the control group (P<0.01); there were differences of statistical significance between the PWT values of the SNL + EA and SNL groups on postoperative days 14 and 21 (P<0.05). Postoperatively, the PWT of the hindpaw on the uninjured-side was significantly lower in the SNL group when compared with that of the control group on days 10, 14 and 21 (P<0.05). Following the EA treatment, axonal demyelination was reduced and vascular proliferation was observed within the visual field. In addition, following the EA treatment, BDNF expression levels in the spinal dorsal horn increased (P<0.05), while the expression of P2X4 was not different from that in the SNL group. EA exerted an analgesic effect on the SNL model in a time-dependent manner, and improved the blood supply to the nerve root. Following the EA treatment, the expression of P2X4 did not change significantly compared with that in the SNL group, whereas the spinal secretion of BDNF increased. However, the exact mechanism requires further study.
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spelling pubmed-43169882015-02-09 Analgesic mechanism of electroacupuncture in a rat L5 spinal nerve ligation model XUE, CHUNCHUN XIE, LEI LI, XIA CAI, JIANFENG GU, ZHEN WANG, KAIQIANG Exp Ther Med Articles The aim of this study was to investigate the analgesic mechanism of electroacupuncture (EA) in the treatment of neuropathological pain. A total of 60 Sprague-Dawley rats were randomly divided into three groups, namely the spinal nerve ligation (SNL), electroacupuncture (SNL + EA) and normal control groups, with 20 rats in each group. The up-down method was used to determine the bipedal 50% mechanical paw withdrawal threshold (PWT). The ultrastructure of the injured-side L5 nerve root (n=6) was observed by electron microscopy. The mRNA levels of brain-derived neurotrophic factor (BDNF) and purinergic receptor P2X, ligand-gated ion channel 4 (P2X4) in the spinal cord (n=14) were determined by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The postoperative PWT of the injured-side hindpaw in the SNL group at each time point was lower than that in the control group (P<0.01); there were differences of statistical significance between the PWT values of the SNL + EA and SNL groups on postoperative days 14 and 21 (P<0.05). Postoperatively, the PWT of the hindpaw on the uninjured-side was significantly lower in the SNL group when compared with that of the control group on days 10, 14 and 21 (P<0.05). Following the EA treatment, axonal demyelination was reduced and vascular proliferation was observed within the visual field. In addition, following the EA treatment, BDNF expression levels in the spinal dorsal horn increased (P<0.05), while the expression of P2X4 was not different from that in the SNL group. EA exerted an analgesic effect on the SNL model in a time-dependent manner, and improved the blood supply to the nerve root. Following the EA treatment, the expression of P2X4 did not change significantly compared with that in the SNL group, whereas the spinal secretion of BDNF increased. However, the exact mechanism requires further study. D.A. Spandidos 2015-03 2015-01-02 /pmc/articles/PMC4316988/ /pubmed/25667665 http://dx.doi.org/10.3892/etm.2015.2165 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
XUE, CHUNCHUN
XIE, LEI
LI, XIA
CAI, JIANFENG
GU, ZHEN
WANG, KAIQIANG
Analgesic mechanism of electroacupuncture in a rat L5 spinal nerve ligation model
title Analgesic mechanism of electroacupuncture in a rat L5 spinal nerve ligation model
title_full Analgesic mechanism of electroacupuncture in a rat L5 spinal nerve ligation model
title_fullStr Analgesic mechanism of electroacupuncture in a rat L5 spinal nerve ligation model
title_full_unstemmed Analgesic mechanism of electroacupuncture in a rat L5 spinal nerve ligation model
title_short Analgesic mechanism of electroacupuncture in a rat L5 spinal nerve ligation model
title_sort analgesic mechanism of electroacupuncture in a rat l5 spinal nerve ligation model
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316988/
https://www.ncbi.nlm.nih.gov/pubmed/25667665
http://dx.doi.org/10.3892/etm.2015.2165
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