Cargando…

Bavachalcone Enhances RORα Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells

The circadian clock regulates many aspects of (patho)physiology in the central nervous system and in the peripheral tissues. RAR-related orphan receptor α (RORα), an orphan nuclear receptor, is involved in circadian rhythm regulation, including regulation of cardiovascular function. Bavachalcone, a...

Descripción completa

Detalles Bibliográficos
Autores principales: Dang, Yanqi, Ling, Shuang, Ma, Jing, Ni, Rongzhen, Xu, Jin-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493309/
https://www.ncbi.nlm.nih.gov/pubmed/26199639
http://dx.doi.org/10.1155/2015/920431
_version_ 1782379891312820224
author Dang, Yanqi
Ling, Shuang
Ma, Jing
Ni, Rongzhen
Xu, Jin-Wen
author_facet Dang, Yanqi
Ling, Shuang
Ma, Jing
Ni, Rongzhen
Xu, Jin-Wen
author_sort Dang, Yanqi
collection PubMed
description The circadian clock regulates many aspects of (patho)physiology in the central nervous system and in the peripheral tissues. RAR-related orphan receptor α (RORα), an orphan nuclear receptor, is involved in circadian rhythm regulation, including regulation of cardiovascular function. Bavachalcone, a prenylchalcone, is a major bioactive chalcone isolated from Psoralea corylifolia. This natural ingredient activated RORα1 luciferase reporter activity on drug screening. In addition, bavachalcone induced RORα1 expression in mRNA and protein levels in a dose-dependent manner and enhanced the circadian amplitude of Bmal1 mRNA expression after serum shock. Moreover, bavachalcone suppressed senescence in human endothelial cells and mRNA expression of p16(ink4a) (a marker of replicative senescence) and IL-1α (a proinflammatory cytokine of the senescence-associated secretory phenotype). These inhibitory effects were partially reversed by the RORα inhibitor VPR-66. Our results demonstrate that bavachalcone, as a natural medicine ingredient, has a pharmacological function in regulating RORα1.
format Online
Article
Text
id pubmed-4493309
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-44933092015-07-21 Bavachalcone Enhances RORα Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells Dang, Yanqi Ling, Shuang Ma, Jing Ni, Rongzhen Xu, Jin-Wen Evid Based Complement Alternat Med Research Article The circadian clock regulates many aspects of (patho)physiology in the central nervous system and in the peripheral tissues. RAR-related orphan receptor α (RORα), an orphan nuclear receptor, is involved in circadian rhythm regulation, including regulation of cardiovascular function. Bavachalcone, a prenylchalcone, is a major bioactive chalcone isolated from Psoralea corylifolia. This natural ingredient activated RORα1 luciferase reporter activity on drug screening. In addition, bavachalcone induced RORα1 expression in mRNA and protein levels in a dose-dependent manner and enhanced the circadian amplitude of Bmal1 mRNA expression after serum shock. Moreover, bavachalcone suppressed senescence in human endothelial cells and mRNA expression of p16(ink4a) (a marker of replicative senescence) and IL-1α (a proinflammatory cytokine of the senescence-associated secretory phenotype). These inhibitory effects were partially reversed by the RORα inhibitor VPR-66. Our results demonstrate that bavachalcone, as a natural medicine ingredient, has a pharmacological function in regulating RORα1. Hindawi Publishing Corporation 2015 2015-06-23 /pmc/articles/PMC4493309/ /pubmed/26199639 http://dx.doi.org/10.1155/2015/920431 Text en Copyright © 2015 Yanqi Dang et al. https://creativecommons.org/licenses/by/3.0/ 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
Dang, Yanqi
Ling, Shuang
Ma, Jing
Ni, Rongzhen
Xu, Jin-Wen
Bavachalcone Enhances RORα Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells
title Bavachalcone Enhances RORα Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells
title_full Bavachalcone Enhances RORα Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells
title_fullStr Bavachalcone Enhances RORα Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells
title_full_unstemmed Bavachalcone Enhances RORα Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells
title_short Bavachalcone Enhances RORα Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells
title_sort bavachalcone enhances rorα expression, controls bmal1 circadian transcription, and depresses cellular senescence in human endothelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493309/
https://www.ncbi.nlm.nih.gov/pubmed/26199639
http://dx.doi.org/10.1155/2015/920431
work_keys_str_mv AT dangyanqi bavachalconeenhancesroraexpressioncontrolsbmal1circadiantranscriptionanddepressescellularsenescenceinhumanendothelialcells
AT lingshuang bavachalconeenhancesroraexpressioncontrolsbmal1circadiantranscriptionanddepressescellularsenescenceinhumanendothelialcells
AT majing bavachalconeenhancesroraexpressioncontrolsbmal1circadiantranscriptionanddepressescellularsenescenceinhumanendothelialcells
AT nirongzhen bavachalconeenhancesroraexpressioncontrolsbmal1circadiantranscriptionanddepressescellularsenescenceinhumanendothelialcells
AT xujinwen bavachalconeenhancesroraexpressioncontrolsbmal1circadiantranscriptionanddepressescellularsenescenceinhumanendothelialcells