Cargando…

Xiao Yao San against Corticosterone-Induced Stress Injury via Upregulating Glucocorticoid Receptor Reaction Element Transcriptional Activity

Previous studies have revealed that uncontrollable stress can impair the synaptic plasticity and firing property of hippocampal neurons, which influenced various hippocampal-dependent tasks including memory, cognition, behavior, and mood. In this work, we had investigated the effects and mechanisms...

Descripción completa

Detalles Bibliográficos
Autores principales: Cao, Guoping, Gong, Shenglan, Zhang, Fengxue, Fu, Wenjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086362/
https://www.ncbi.nlm.nih.gov/pubmed/27822288
http://dx.doi.org/10.1155/2016/5850739
_version_ 1782463723541102592
author Cao, Guoping
Gong, Shenglan
Zhang, Fengxue
Fu, Wenjun
author_facet Cao, Guoping
Gong, Shenglan
Zhang, Fengxue
Fu, Wenjun
author_sort Cao, Guoping
collection PubMed
description Previous studies have revealed that uncontrollable stress can impair the synaptic plasticity and firing property of hippocampal neurons, which influenced various hippocampal-dependent tasks including memory, cognition, behavior, and mood. In this work, we had investigated the effects and mechanisms of the Chinese herbal medicine Xiao Yao San (XYS) against corticosterone-induced stress injury in primary hippocampal neurons (PHN) cells. We found that XYS and RU38486 could increase cell viabilities and decrease cell apoptosis by MTT, immunofluorescence, and flow cytometry assays. In addition, we observed that XYS notably inhibited the nuclear translocation of GR and upregulated the mRNA and protein expressions levels of Caveolin-1, GR, BDNF, TrkB, and FKBP4. However, XYS downregulated the FKBP51 expressions. Furthermore, the results of the electrophoretic mobility shift assay (EMSA) and double luciferase reporter gene detection indicated that FKBP4 promotes the transcriptional activity of GR reaction element (GRE) by binding with GR, and FKBP51 processed the opposite action. The in vivo experiment also proved the functions of XYS. These results suggested that XYS showed an efficient neuroprotection against corticosterone-induced stress injury in PHN cells by upregulating GRE transcriptional activity, which should be developed as a potential candidate for treating stress injury in the future.
format Online
Article
Text
id pubmed-5086362
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-50863622016-11-07 Xiao Yao San against Corticosterone-Induced Stress Injury via Upregulating Glucocorticoid Receptor Reaction Element Transcriptional Activity Cao, Guoping Gong, Shenglan Zhang, Fengxue Fu, Wenjun Evid Based Complement Alternat Med Research Article Previous studies have revealed that uncontrollable stress can impair the synaptic plasticity and firing property of hippocampal neurons, which influenced various hippocampal-dependent tasks including memory, cognition, behavior, and mood. In this work, we had investigated the effects and mechanisms of the Chinese herbal medicine Xiao Yao San (XYS) against corticosterone-induced stress injury in primary hippocampal neurons (PHN) cells. We found that XYS and RU38486 could increase cell viabilities and decrease cell apoptosis by MTT, immunofluorescence, and flow cytometry assays. In addition, we observed that XYS notably inhibited the nuclear translocation of GR and upregulated the mRNA and protein expressions levels of Caveolin-1, GR, BDNF, TrkB, and FKBP4. However, XYS downregulated the FKBP51 expressions. Furthermore, the results of the electrophoretic mobility shift assay (EMSA) and double luciferase reporter gene detection indicated that FKBP4 promotes the transcriptional activity of GR reaction element (GRE) by binding with GR, and FKBP51 processed the opposite action. The in vivo experiment also proved the functions of XYS. These results suggested that XYS showed an efficient neuroprotection against corticosterone-induced stress injury in PHN cells by upregulating GRE transcriptional activity, which should be developed as a potential candidate for treating stress injury in the future. Hindawi Publishing Corporation 2016 2016-10-16 /pmc/articles/PMC5086362/ /pubmed/27822288 http://dx.doi.org/10.1155/2016/5850739 Text en Copyright © 2016 Guoping Cao et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cao, Guoping
Gong, Shenglan
Zhang, Fengxue
Fu, Wenjun
Xiao Yao San against Corticosterone-Induced Stress Injury via Upregulating Glucocorticoid Receptor Reaction Element Transcriptional Activity
title Xiao Yao San against Corticosterone-Induced Stress Injury via Upregulating Glucocorticoid Receptor Reaction Element Transcriptional Activity
title_full Xiao Yao San against Corticosterone-Induced Stress Injury via Upregulating Glucocorticoid Receptor Reaction Element Transcriptional Activity
title_fullStr Xiao Yao San against Corticosterone-Induced Stress Injury via Upregulating Glucocorticoid Receptor Reaction Element Transcriptional Activity
title_full_unstemmed Xiao Yao San against Corticosterone-Induced Stress Injury via Upregulating Glucocorticoid Receptor Reaction Element Transcriptional Activity
title_short Xiao Yao San against Corticosterone-Induced Stress Injury via Upregulating Glucocorticoid Receptor Reaction Element Transcriptional Activity
title_sort xiao yao san against corticosterone-induced stress injury via upregulating glucocorticoid receptor reaction element transcriptional activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086362/
https://www.ncbi.nlm.nih.gov/pubmed/27822288
http://dx.doi.org/10.1155/2016/5850739
work_keys_str_mv AT caoguoping xiaoyaosanagainstcorticosteroneinducedstressinjuryviaupregulatingglucocorticoidreceptorreactionelementtranscriptionalactivity
AT gongshenglan xiaoyaosanagainstcorticosteroneinducedstressinjuryviaupregulatingglucocorticoidreceptorreactionelementtranscriptionalactivity
AT zhangfengxue xiaoyaosanagainstcorticosteroneinducedstressinjuryviaupregulatingglucocorticoidreceptorreactionelementtranscriptionalactivity
AT fuwenjun xiaoyaosanagainstcorticosteroneinducedstressinjuryviaupregulatingglucocorticoidreceptorreactionelementtranscriptionalactivity