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Glossogyne tenuifolia Attenuates Proliferation and Migration of Vascular Smooth Muscle Cells

Authors :
Shih-Wei Wang
Yung-Chuan Lu
Tzu-Hsien Chang
Chi-Chang Chang
Chin-Feng Hsuan
Jer-Yiing Houng
I-Ting Tsai
Ya-Ling Chen
Source :
Molecules, Volume 25, Issue 24, Molecules, Vol 25, Iss 5832, p 5832 (2020)
Publication Year :
2020
Publisher :
MDPI, 2020.

Abstract

The proliferation and migration of vascular smooth muscle cells (VSMCs) are essential in the pathogenesis of various vascular diseases, such as atherosclerosis and restenosis. Among the mediators of VSMC during atherosclerosis development, platelet-derived growth factor (PDGF)-BB is a potent mitogen for VSMCs and greatly contributes to the intimal accumulation of VSMCs. Glossogyne tenuifolia (GT, Xiang-Ru) is a traditional antipyretic and hepatoprotective herb from Penghu Island, Taiwan. This study evaluated the inhibitory effect of GT ethanol extract (GTE) and GT water extract (GTW) on proliferative and migratory activities in PDGF-BB-induced VSMCs. The experimental results demonstrated that GTE significantly inhibited the PDGF-BB-stimulated VSMC proliferation and migration, as shown by MTT, wound healing, and Boyden chamber assays. GTE was found to have a much more potent inhibitory activity than GTW. Based on the Western blot analysis, GTE significantly blocked the PDGF-BB-induced phosphorylation of NF-&kappa<br />B and mitogen-activated protein kinase (MAPK) pathways, including extracellular signal-regulated kinase (ERK), p38, and JNK, in VSMCs. In addition, GTE retarded the PDGF-BB-mediated migration through the suppression of matrix metalloproteinase (MMP)-2 and MMP-9 expression in VSMCs. Three main ingredients of GT&mdash<br />chlorogenic acid, luteolin-7-glucoside, and luteolin&mdash<br />all showed significant anti-proliferative effects on PDGF-BB-induced VSMCs. As a whole, our findings indicated that GTE has the potential to be a therapeutic agent to prevent or treat restenosis or atherosclerosis.

Details

Language :
English
ISSN :
14203049
Volume :
25
Issue :
24
Database :
OpenAIRE
Journal :
Molecules
Accession number :
edsair.doi.dedup.....255e75cb55b49926b4cdc3ec0b4aecfe