Xanthohumol Blocks Proliferation and Migration of Vascular Smooth Muscle Cellsin Vitroand Reduces Neointima Formationin Vivo
Author(s) -
Rongxia Liu,
Elke H. Heiß,
Daniel Schachner,
Baohong Jiang,
Wanhui Liu,
Johannes M. Breuss,
Verena M. Dirsch,
Atanas G. Atanasov
Publication year - 2017
Publication title -
journal of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 139
eISSN - 1520-6025
pISSN - 0163-3864
DOI - 10.1021/acs.jnatprod.7b00268
Subject(s) - neointima , vascular smooth muscle , in vivo , xanthohumol , platelet derived growth factor receptor , microbiology and biotechnology , in vitro , cell growth , platelet derived growth factor , chemistry , biology , growth factor , pharmacology , biochemistry , medicine , endocrinology , smooth muscle , restenosis , ecology , receptor , key (lock) , stent
Xanthohumol (1) is a principal prenylated chalcone found in hops. The aim of this study was to examine its influence on platelet-derived growth factor (PDGF)-BB-triggered vascular smooth muscle cell (VSMC) proliferation and migration in vitro and on experimentally induced neointima formation in vivo. Quantification of resazurin conversion indicated that 1 can inhibit PDGF-BB-induced VSMC proliferation concentration-dependently (IC 50 = 3.49 μM). Furthermore, in a wound-healing assay 1 potently suppresses PDGF-BB-induced VSMC migration at 15 μM. Tested in a mouse femoral artery cuff model, 1 significantly reduces neointima formation. Taken together, we show that 1 represses PDGF-BB-induced VSMC proliferation and migration in vitro as well as neointima formation in vivo. This novel activity suggests 1 as an interesting candidate for further studies addressing a possible therapeutic application to counteract vascular proliferative disease.
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