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Cited 30 time in webofscience Cited 31 time in scopus
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Transcriptional up-regulation of antioxidant genes by PPAR delta inhibits angiotensin II-induced premature senescence in vascular smooth muscle cells

Authors
Kim, Hyo JungHam, Sun AhPaek, Kyung ShinHwang, Jung SeokJung, Si YoungKim, Min YoungJin, HannaKang, Eun SilWoo, Im SunKim, Hye JungLee, Jae HeunChang, Ki ChurlHan, Chang WooSeo, Han Geuk
Issue Date
25-Mar-2011
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Angiotensin II; Antioxidant genes; Senescence; PPAR delta; ROS
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.406, no.4, pp 564 - 569
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
406
Number
4
Start Page
564
End Page
569
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/23800
DOI
10.1016/j.bbrc.2011.02.091
ISSN
0006-291X
1090-2104
Abstract
This study evaluated peroxisome proliferator-activated receptor (PPAR) delta as a potential target for therapeutic intervention in Ang II-induced senescence in human vascular smooth muscle cells (hVSMCs). Activation of PPAR delta by GW501516, a specific agonist of PPAR delta, significantly inhibited the Ang II-induced premature senescence of hVSMCs. Agonist-activated PPAR delta suppressed the generation of Ang II-triggered reactive oxygen species (ROS) with a concomitant reduction in DNA damage. Notably, GW501516 up-regulated the expression of antioxidant genes, such as glutathione peroxidase 1, thioredoxin 1, manganese superoxide dismutase and heme oxygenase 1. siRNA-mediated down-regulation of these antioxidant genes almost completely abolished the effects of GW501516 on ROS production and premature senescence in hVSMCs treated with Ang II. Taken together, the enhanced transcription of antioxidant genes is responsible for the PPAR delta-mediated inhibition of premature senescence through sequestration of ROS in hVSMCs treated with Ang II. (C) 2011 Elsevier Inc. All rights reserved.
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