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Protocatechuic aldehyde inhibits migration and proliferation of vascular smooth muscle cells and intravascular thrombosis.

Authors
 Chang Yoon Moon  ;  Cheol Ryong Ku  ;  Yoon Hee Cho  ;  Eun Jig Lee 
Citation
 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Vol.423(1) : 116-121, 2012 
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN
 0006-291X 
Issue Date
2012
MeSH
Animals ; Anticoagulants/pharmacology* ; Antioxidants/pharmacology* ; Benzaldehydes/pharmacology* ; Blood Platelets/drug effects ; Catechols/pharmacology* ; Cell Movement/drug effects* ; Cell Proliferation/drug effects* ; Cells, Cultured ; MAP Kinase Signaling System/drug effects ; Male ; Muscle, Smooth, Vascular/cytology ; Muscle, Smooth, Vascular/drug effects* ; Muscle, Smooth, Vascular/metabolism ; Myocytes, Smooth Muscle/drug effects* ; Myocytes, Smooth Muscle/metabolism ; Myocytes, Smooth Muscle/physiology ; Proto-Oncogene Proteins c-akt ; Rats ; Rats, Sprague-Dawley ; Reactive Oxygen Species/antagonists & inhibitors ; Reactive Oxygen Species/metabolism ; S Phase Cell Cycle Checkpoints/drug effects ; Thrombosis/blood ; Thrombosis/physiopathology*
Keywords
Protocatechuic aldehyde ; Anti-oxidant ; Atherosclerosis ; Migration ; Proliferation ; Anti-platelet ; PDGF
Abstract
The migration and proliferation of vascular smooth muscle cells (VSMCs) and formation of intravascular thrombosis play crucial roles in the development of atherosclerotic lesions. This study examined the effects of protocatechuic aldehyde (PCA), a compound isolated from the aqueous extract of the root of Salvia miltiorrhiza, an herb used in traditional Chinese medicine to treat a variety of vascular diseases, on the migration and proliferation of VSMCs and platelets due to platelet-derived growth factor (PDGF). DNA 5-bromo-2'-deoxy-uridine (BrdU) incorporation and wound-healing assays indicated that PCA significantly attenuated PDGF-induced proliferation and migration of VSMCs at a pharmacologically relevant concentration (100 μM). On a molecular level, we observed down-regulation of the phosphatidylinositol 3-kinase (PI3K)/Akt and the mitogen-activated protein kinase (MAPK) pathways, both of which regulate key enzymes associated with migration and proliferation. We also found that PCA induced S-phase arrest of the VSMC cell cycle and suppressed cyclin D2 expression. In addition, PCA inhibited PDGF-BB-stimulated reactive oxygen species production in VSMCs, indicating that PCA's antioxidant properties may contribute to its suppression of PDGF-induced migration and proliferation in VSMCs. Finally, PCA exhibited an anti-thrombotic effect related to its inhibition of platelet aggregation, confirmed with an aggregometer. Together, these findings suggest a potential therapeutic role of PCA in the treatment of atherosclerosis and angioplasty-induced vascular restenosis.
Full Text
http://www.sciencedirect.com/science/article/pii/S0006291X12009825
DOI
22640742
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
Yonsei Authors
Ku, Cheol Ryong(구철룡) ORCID logo https://orcid.org/0000-0001-8693-9630
Lee, Eun Jig(이은직) ORCID logo https://orcid.org/0000-0002-9876-8370
Cho, Yoon Hee(조윤희)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/89699
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