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Thymosin Beta 4 Is Involved in the Development of Electroacupuncture Tolerance

Background: Electroacupuncture (EA) tolerance, a negative therapeutic effect, is a gradual decline in antinociception because of its repeated or prolonged use. This study aims to explore the role of thymosin beta 4 (Tβ4), having neuro-protection properties, in EA tolerance (EAT). Methods: Rats were...

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Autores principales: Wan, Juan, Ding, Yi, Nan, Sha, Zhang, Qiulin, Sun, Jinrui, Suo, Chuanguang, Ding, Mingxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444270/
https://www.ncbi.nlm.nih.gov/pubmed/30971892
http://dx.doi.org/10.3389/fncel.2019.00075
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author Wan, Juan
Ding, Yi
Nan, Sha
Zhang, Qiulin
Sun, Jinrui
Suo, Chuanguang
Ding, Mingxing
author_facet Wan, Juan
Ding, Yi
Nan, Sha
Zhang, Qiulin
Sun, Jinrui
Suo, Chuanguang
Ding, Mingxing
author_sort Wan, Juan
collection PubMed
description Background: Electroacupuncture (EA) tolerance, a negative therapeutic effect, is a gradual decline in antinociception because of its repeated or prolonged use. This study aims to explore the role of thymosin beta 4 (Tβ4), having neuro-protection properties, in EA tolerance (EAT). Methods: Rats were treated with EA once daily for eight consecutive days to establish EAT, effect of Tβ4 on the development of EAT was determined through microinjection of Tβ4 antibody and siRNA into the cerebroventricle. The mRNA and protein expression profiles of Tβ4, opioid peptides (enkephalin, dynorphin and endorphin), and anti-opioid peptides (cholecystokinin octapeptide, CCK-8 and orphanin FQ, OFQ), and mu opioid receptor (MOR) and CCK B receptor (CCKBR) in the brain areas (hypothalamus, thalamus, cortex, midbrain and medulla) were characterized after Tβ4 siRNA was administered. Results: Tβ4 levels were increased at day 1, 4, and 8 and negatively correlated with the changes of tail flick latency in all areas. Tβ4 antibody and siRNA postponed EAT. Tβ4 siRNA caused decreased Tβ4 levels in all areas, which resulted in increased enkephalin, dynorphin, endorphin and MOR levels in most measured areas during repeated EA, but unchanged OFQ, CCK-8, and CCKBR levels in most measured areas. Tβ4 levels were negatively correlated with enkephalin, dynorphin, endorphin, or MOR levels in all areas except medulla, while positively correlated with OFQ and CCK-8 levels in some areas. Conclusion: These results confirmed Tβ4 facilitates EAT probably through negatively changing endogenous opioid peptides and their receptors and positively influencing anti-opioid peptides in the central nervous system.
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spelling pubmed-64442702019-04-10 Thymosin Beta 4 Is Involved in the Development of Electroacupuncture Tolerance Wan, Juan Ding, Yi Nan, Sha Zhang, Qiulin Sun, Jinrui Suo, Chuanguang Ding, Mingxing Front Cell Neurosci Neuroscience Background: Electroacupuncture (EA) tolerance, a negative therapeutic effect, is a gradual decline in antinociception because of its repeated or prolonged use. This study aims to explore the role of thymosin beta 4 (Tβ4), having neuro-protection properties, in EA tolerance (EAT). Methods: Rats were treated with EA once daily for eight consecutive days to establish EAT, effect of Tβ4 on the development of EAT was determined through microinjection of Tβ4 antibody and siRNA into the cerebroventricle. The mRNA and protein expression profiles of Tβ4, opioid peptides (enkephalin, dynorphin and endorphin), and anti-opioid peptides (cholecystokinin octapeptide, CCK-8 and orphanin FQ, OFQ), and mu opioid receptor (MOR) and CCK B receptor (CCKBR) in the brain areas (hypothalamus, thalamus, cortex, midbrain and medulla) were characterized after Tβ4 siRNA was administered. Results: Tβ4 levels were increased at day 1, 4, and 8 and negatively correlated with the changes of tail flick latency in all areas. Tβ4 antibody and siRNA postponed EAT. Tβ4 siRNA caused decreased Tβ4 levels in all areas, which resulted in increased enkephalin, dynorphin, endorphin and MOR levels in most measured areas during repeated EA, but unchanged OFQ, CCK-8, and CCKBR levels in most measured areas. Tβ4 levels were negatively correlated with enkephalin, dynorphin, endorphin, or MOR levels in all areas except medulla, while positively correlated with OFQ and CCK-8 levels in some areas. Conclusion: These results confirmed Tβ4 facilitates EAT probably through negatively changing endogenous opioid peptides and their receptors and positively influencing anti-opioid peptides in the central nervous system. Frontiers Media S.A. 2019-03-26 /pmc/articles/PMC6444270/ /pubmed/30971892 http://dx.doi.org/10.3389/fncel.2019.00075 Text en Copyright © 2019 Wan, Ding, Nan, Zhang, Sun, Suo and Ding. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Wan, Juan
Ding, Yi
Nan, Sha
Zhang, Qiulin
Sun, Jinrui
Suo, Chuanguang
Ding, Mingxing
Thymosin Beta 4 Is Involved in the Development of Electroacupuncture Tolerance
title Thymosin Beta 4 Is Involved in the Development of Electroacupuncture Tolerance
title_full Thymosin Beta 4 Is Involved in the Development of Electroacupuncture Tolerance
title_fullStr Thymosin Beta 4 Is Involved in the Development of Electroacupuncture Tolerance
title_full_unstemmed Thymosin Beta 4 Is Involved in the Development of Electroacupuncture Tolerance
title_short Thymosin Beta 4 Is Involved in the Development of Electroacupuncture Tolerance
title_sort thymosin beta 4 is involved in the development of electroacupuncture tolerance
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444270/
https://www.ncbi.nlm.nih.gov/pubmed/30971892
http://dx.doi.org/10.3389/fncel.2019.00075
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