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Two kinds of transcription factors mediate chronic morphine-induced decrease in miR-105 in medial prefrontal cortex of rats
Chronic morphine administration alters gene expression in different brain regions, an effect which may contribute to plastic changes associated with addictive behavior. This change in gene expression is most possibly mediated by addictive drug-induced epigenetic remodeling of gene expression program...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622915/ https://www.ncbi.nlm.nih.gov/pubmed/36316324 http://dx.doi.org/10.1038/s41398-022-02222-3 |
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author | Zhang, Junfang Guo, Xinli Cai, Zhangyin Pan, Yan Yang, Hao Fu, Yali Cao, Zixuan Wen, Yaxian Lei, Chao Chu, Chenshan Yuan, Yu Cui, Dongyang Gao, Pengyu Lai, Bin Zheng, Ping |
author_facet | Zhang, Junfang Guo, Xinli Cai, Zhangyin Pan, Yan Yang, Hao Fu, Yali Cao, Zixuan Wen, Yaxian Lei, Chao Chu, Chenshan Yuan, Yu Cui, Dongyang Gao, Pengyu Lai, Bin Zheng, Ping |
author_sort | Zhang, Junfang |
collection | PubMed |
description | Chronic morphine administration alters gene expression in different brain regions, an effect which may contribute to plastic changes associated with addictive behavior. This change in gene expression is most possibly mediated by addictive drug-induced epigenetic remodeling of gene expression programs. Our previous studies showed that chronic morphine-induced decrease of miR-105 in the medial prefrontal cortex (mPFC) contributed to context-induced retrieval of morphine withdrawal memory. However, how chronic morphine treatment decreases miR-105 in the mPFC still remains unknown. The present study shows that chronic morphine induces addiction-related change in miR-105 in the mPFC via two kinds of transcription factors: the first transcription factor is CREB activated by mu receptors-ERK-p90RSK signaling pathway and the second transcription factor is glucocorticoid receptor (GR), which as a negative transcription factor, mediates chronic morphine-induced decrease in miR-105 in the mPFC of rats. |
format | Online Article Text |
id | pubmed-9622915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96229152022-11-02 Two kinds of transcription factors mediate chronic morphine-induced decrease in miR-105 in medial prefrontal cortex of rats Zhang, Junfang Guo, Xinli Cai, Zhangyin Pan, Yan Yang, Hao Fu, Yali Cao, Zixuan Wen, Yaxian Lei, Chao Chu, Chenshan Yuan, Yu Cui, Dongyang Gao, Pengyu Lai, Bin Zheng, Ping Transl Psychiatry Article Chronic morphine administration alters gene expression in different brain regions, an effect which may contribute to plastic changes associated with addictive behavior. This change in gene expression is most possibly mediated by addictive drug-induced epigenetic remodeling of gene expression programs. Our previous studies showed that chronic morphine-induced decrease of miR-105 in the medial prefrontal cortex (mPFC) contributed to context-induced retrieval of morphine withdrawal memory. However, how chronic morphine treatment decreases miR-105 in the mPFC still remains unknown. The present study shows that chronic morphine induces addiction-related change in miR-105 in the mPFC via two kinds of transcription factors: the first transcription factor is CREB activated by mu receptors-ERK-p90RSK signaling pathway and the second transcription factor is glucocorticoid receptor (GR), which as a negative transcription factor, mediates chronic morphine-induced decrease in miR-105 in the mPFC of rats. Nature Publishing Group UK 2022-10-31 /pmc/articles/PMC9622915/ /pubmed/36316324 http://dx.doi.org/10.1038/s41398-022-02222-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Junfang Guo, Xinli Cai, Zhangyin Pan, Yan Yang, Hao Fu, Yali Cao, Zixuan Wen, Yaxian Lei, Chao Chu, Chenshan Yuan, Yu Cui, Dongyang Gao, Pengyu Lai, Bin Zheng, Ping Two kinds of transcription factors mediate chronic morphine-induced decrease in miR-105 in medial prefrontal cortex of rats |
title | Two kinds of transcription factors mediate chronic morphine-induced decrease in miR-105 in medial prefrontal cortex of rats |
title_full | Two kinds of transcription factors mediate chronic morphine-induced decrease in miR-105 in medial prefrontal cortex of rats |
title_fullStr | Two kinds of transcription factors mediate chronic morphine-induced decrease in miR-105 in medial prefrontal cortex of rats |
title_full_unstemmed | Two kinds of transcription factors mediate chronic morphine-induced decrease in miR-105 in medial prefrontal cortex of rats |
title_short | Two kinds of transcription factors mediate chronic morphine-induced decrease in miR-105 in medial prefrontal cortex of rats |
title_sort | two kinds of transcription factors mediate chronic morphine-induced decrease in mir-105 in medial prefrontal cortex of rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622915/ https://www.ncbi.nlm.nih.gov/pubmed/36316324 http://dx.doi.org/10.1038/s41398-022-02222-3 |
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