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Chronic Stress Is Associated with Pain Precipitation and Elevation in DeltaFosb Expression

A number of acute or repeated stimuli can induce expression of DeltaFosB (ΔFosB), a transcription factor derived from the fosB gene (an osteosarcoma viral oncogene) via alternative splicing. ΔFosB protein is currently viewed as a ‘molecular switch’ to repeated stimuli that gradually converts acute r...

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Autores principales: Wang, Hang, Tao, Xinrong, Huang, Si-Ting, Wu, Liang, Tang, Hui-Li, Song, Ying, Zhang, Gongliang, Zhang, Yong-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884751/
https://www.ncbi.nlm.nih.gov/pubmed/27303299
http://dx.doi.org/10.3389/fphar.2016.00138
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author Wang, Hang
Tao, Xinrong
Huang, Si-Ting
Wu, Liang
Tang, Hui-Li
Song, Ying
Zhang, Gongliang
Zhang, Yong-Mei
author_facet Wang, Hang
Tao, Xinrong
Huang, Si-Ting
Wu, Liang
Tang, Hui-Li
Song, Ying
Zhang, Gongliang
Zhang, Yong-Mei
author_sort Wang, Hang
collection PubMed
description A number of acute or repeated stimuli can induce expression of DeltaFosB (ΔFosB), a transcription factor derived from the fosB gene (an osteosarcoma viral oncogene) via alternative splicing. ΔFosB protein is currently viewed as a ‘molecular switch’ to repeated stimuli that gradually converts acute responses into relatively stable adaptations underlying long-term neural and behavioral plasticity. ΔFosB has received extensive attention in drug addition, depression, and stress adaptation, but changes in ΔFosB protein expression during pain is not fully understood. In this study we explored ΔFosB expression in the medial prefrontal cortex (mPFC) of rats experiencing chronic or acute stress-induced pain. Our data reveal that chronic pain induced by neonatal colorectal distension, chronic constriction injury (CCI) of the sciatic nerve, or maternal separation was associated with an increase in ΔfosB protein expression in mPFC, but acute application of acetic acid or zymosan did not alter the ΔFosB protein expression. ΔFosB expression in the rat visual cortex, a non pain-related brain region, did not change in response to (CCI) of the sciatic nerve and acetic acid treatment. In conclusion, our results indicate that ΔFosB protein expression is significantly elevated in rats that have experienced chronic pain and stress, but not acute pain. The ΔFosB protein may serve as an important transcription factor for chronic stress-induced pain. Further research is needed to improve the understanding of both the upstream signaling leading to ΔFosB protein expression as well as the regulation of ΔFosB gene expression in cortical neurons.
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spelling pubmed-48847512016-06-14 Chronic Stress Is Associated with Pain Precipitation and Elevation in DeltaFosb Expression Wang, Hang Tao, Xinrong Huang, Si-Ting Wu, Liang Tang, Hui-Li Song, Ying Zhang, Gongliang Zhang, Yong-Mei Front Pharmacol Pharmacology A number of acute or repeated stimuli can induce expression of DeltaFosB (ΔFosB), a transcription factor derived from the fosB gene (an osteosarcoma viral oncogene) via alternative splicing. ΔFosB protein is currently viewed as a ‘molecular switch’ to repeated stimuli that gradually converts acute responses into relatively stable adaptations underlying long-term neural and behavioral plasticity. ΔFosB has received extensive attention in drug addition, depression, and stress adaptation, but changes in ΔFosB protein expression during pain is not fully understood. In this study we explored ΔFosB expression in the medial prefrontal cortex (mPFC) of rats experiencing chronic or acute stress-induced pain. Our data reveal that chronic pain induced by neonatal colorectal distension, chronic constriction injury (CCI) of the sciatic nerve, or maternal separation was associated with an increase in ΔfosB protein expression in mPFC, but acute application of acetic acid or zymosan did not alter the ΔFosB protein expression. ΔFosB expression in the rat visual cortex, a non pain-related brain region, did not change in response to (CCI) of the sciatic nerve and acetic acid treatment. In conclusion, our results indicate that ΔFosB protein expression is significantly elevated in rats that have experienced chronic pain and stress, but not acute pain. The ΔFosB protein may serve as an important transcription factor for chronic stress-induced pain. Further research is needed to improve the understanding of both the upstream signaling leading to ΔFosB protein expression as well as the regulation of ΔFosB gene expression in cortical neurons. Frontiers Media S.A. 2016-05-30 /pmc/articles/PMC4884751/ /pubmed/27303299 http://dx.doi.org/10.3389/fphar.2016.00138 Text en Copyright © 2016 Wang, Tao, Huang, Wu, Tang, Song, Zhang and Zhang. 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) or licensor 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 Pharmacology
Wang, Hang
Tao, Xinrong
Huang, Si-Ting
Wu, Liang
Tang, Hui-Li
Song, Ying
Zhang, Gongliang
Zhang, Yong-Mei
Chronic Stress Is Associated with Pain Precipitation and Elevation in DeltaFosb Expression
title Chronic Stress Is Associated with Pain Precipitation and Elevation in DeltaFosb Expression
title_full Chronic Stress Is Associated with Pain Precipitation and Elevation in DeltaFosb Expression
title_fullStr Chronic Stress Is Associated with Pain Precipitation and Elevation in DeltaFosb Expression
title_full_unstemmed Chronic Stress Is Associated with Pain Precipitation and Elevation in DeltaFosb Expression
title_short Chronic Stress Is Associated with Pain Precipitation and Elevation in DeltaFosb Expression
title_sort chronic stress is associated with pain precipitation and elevation in deltafosb expression
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884751/
https://www.ncbi.nlm.nih.gov/pubmed/27303299
http://dx.doi.org/10.3389/fphar.2016.00138
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