Cargando…

Paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder

OBJECTIVE(S): To investigate the effects of paeoniflorin (PEF) on the hypothalamic-pituitary-adrenal (HPA) axis feedback function of post-traumatic stress disorder (PTSD). MATERIALS AND METHODS: Single-prolonged stress (SPS) was used to establish a PTSD-like rat model. The contents of plasma cortico...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Jie, Ye, Weiqiong, Li, Ling, Su, Junfang, Huang, Yunling, Liu, Lingyun, Wu, Lili, Yan, Can
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239430/
https://www.ncbi.nlm.nih.gov/pubmed/32489558
http://dx.doi.org/10.22038/ijbms.2020.41214.9738
_version_ 1783536687538765824
author Chen, Jie
Ye, Weiqiong
Li, Ling
Su, Junfang
Huang, Yunling
Liu, Lingyun
Wu, Lili
Yan, Can
author_facet Chen, Jie
Ye, Weiqiong
Li, Ling
Su, Junfang
Huang, Yunling
Liu, Lingyun
Wu, Lili
Yan, Can
author_sort Chen, Jie
collection PubMed
description OBJECTIVE(S): To investigate the effects of paeoniflorin (PEF) on the hypothalamic-pituitary-adrenal (HPA) axis feedback function of post-traumatic stress disorder (PTSD). MATERIALS AND METHODS: Single-prolonged stress (SPS) was used to establish a PTSD-like rat model. The contents of plasma corticosterone (CORT), adrenocorticotropin hormone (ACTH) and corticotropin-releasing hormone (CRH) were measured by ELISA. Glucocorticoid receptor (GR), mineralocorticoid receptor (MR), adrenocorticotropic hormone-releasing factor I receptor (CRF1R), and adrenocorticotropic hormone-releasing factor II receptor (CRF2R) in the hippocampus and amygdala were measured by RT-PCR and immunohistochemistry. RESULTS: The results showed that on day 8 after SPS, model rats showed enhanced HPA axis negative feedback lasting to day 29. On day 29, plasma CORT levels increased in model rats, while plasma CRH levels had no significant difference on days 8, 22, and 29. The expression of GR and MR of model rats significantly increased in the hippocampus, while the expression of GR, MR, and CRF1R significantly decreased in the amygdala. After 14 days of continuous administration of PEF, the enhanced negative feedback was inhibited, and the plasma CORT level significantly reduced after 21 days of administration. Moreover, PEF could significantly decrease the expression of GR and MR in the hippocampus, and increase the expression of GR, MR, and CRF1R significantly in the amygdala. CONCLUSION: PEF could regulate HPA axis dysfunction in a rat model of PTSD, which may be related to regulating expression of GR and MR in the hippocampus and amygdala and regulating expression of CRF1R in the amygdala.
format Online
Article
Text
id pubmed-7239430
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Mashhad University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-72394302020-06-01 Paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder Chen, Jie Ye, Weiqiong Li, Ling Su, Junfang Huang, Yunling Liu, Lingyun Wu, Lili Yan, Can Iran J Basic Med Sci Original Article OBJECTIVE(S): To investigate the effects of paeoniflorin (PEF) on the hypothalamic-pituitary-adrenal (HPA) axis feedback function of post-traumatic stress disorder (PTSD). MATERIALS AND METHODS: Single-prolonged stress (SPS) was used to establish a PTSD-like rat model. The contents of plasma corticosterone (CORT), adrenocorticotropin hormone (ACTH) and corticotropin-releasing hormone (CRH) were measured by ELISA. Glucocorticoid receptor (GR), mineralocorticoid receptor (MR), adrenocorticotropic hormone-releasing factor I receptor (CRF1R), and adrenocorticotropic hormone-releasing factor II receptor (CRF2R) in the hippocampus and amygdala were measured by RT-PCR and immunohistochemistry. RESULTS: The results showed that on day 8 after SPS, model rats showed enhanced HPA axis negative feedback lasting to day 29. On day 29, plasma CORT levels increased in model rats, while plasma CRH levels had no significant difference on days 8, 22, and 29. The expression of GR and MR of model rats significantly increased in the hippocampus, while the expression of GR, MR, and CRF1R significantly decreased in the amygdala. After 14 days of continuous administration of PEF, the enhanced negative feedback was inhibited, and the plasma CORT level significantly reduced after 21 days of administration. Moreover, PEF could significantly decrease the expression of GR and MR in the hippocampus, and increase the expression of GR, MR, and CRF1R significantly in the amygdala. CONCLUSION: PEF could regulate HPA axis dysfunction in a rat model of PTSD, which may be related to regulating expression of GR and MR in the hippocampus and amygdala and regulating expression of CRF1R in the amygdala. Mashhad University of Medical Sciences 2020-04 /pmc/articles/PMC7239430/ /pubmed/32489558 http://dx.doi.org/10.22038/ijbms.2020.41214.9738 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Chen, Jie
Ye, Weiqiong
Li, Ling
Su, Junfang
Huang, Yunling
Liu, Lingyun
Wu, Lili
Yan, Can
Paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder
title Paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder
title_full Paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder
title_fullStr Paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder
title_full_unstemmed Paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder
title_short Paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder
title_sort paeoniflorin regulates the hypothalamic-pituitary-adrenal axis negative feedback in a rat model of post-traumatic stress disorder
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239430/
https://www.ncbi.nlm.nih.gov/pubmed/32489558
http://dx.doi.org/10.22038/ijbms.2020.41214.9738
work_keys_str_mv AT chenjie paeoniflorinregulatesthehypothalamicpituitaryadrenalaxisnegativefeedbackinaratmodelofposttraumaticstressdisorder
AT yeweiqiong paeoniflorinregulatesthehypothalamicpituitaryadrenalaxisnegativefeedbackinaratmodelofposttraumaticstressdisorder
AT liling paeoniflorinregulatesthehypothalamicpituitaryadrenalaxisnegativefeedbackinaratmodelofposttraumaticstressdisorder
AT sujunfang paeoniflorinregulatesthehypothalamicpituitaryadrenalaxisnegativefeedbackinaratmodelofposttraumaticstressdisorder
AT huangyunling paeoniflorinregulatesthehypothalamicpituitaryadrenalaxisnegativefeedbackinaratmodelofposttraumaticstressdisorder
AT liulingyun paeoniflorinregulatesthehypothalamicpituitaryadrenalaxisnegativefeedbackinaratmodelofposttraumaticstressdisorder
AT wulili paeoniflorinregulatesthehypothalamicpituitaryadrenalaxisnegativefeedbackinaratmodelofposttraumaticstressdisorder
AT yancan paeoniflorinregulatesthehypothalamicpituitaryadrenalaxisnegativefeedbackinaratmodelofposttraumaticstressdisorder