KR 31372, a benzopyran derivative, inhibits oxidized LDL-stimulated proliferation and migration of vascular smooth muscle cells

被引:4
|
作者
Kim, HH
Ha, HJ
Kim, SO
Kim, SK
Yoo, SE
Hong, KW [1 ]
机构
[1] Pusan Natl Univ, Coll Med, Dept Pharmacol, Pusan 609735, South Korea
[2] Yonsei Univ, Seoul 120749, South Korea
[3] Dongbu Hannong Chem Co, Cent Res Inst, Daejon, South Korea
[4] Korea Res Inst Chem Technol, Daejon, South Korea
关键词
KR; 31372; K+ channels; oxidized LDL; migration; antioxidation; PDGF-BB;
D O I
10.1111/j.1472-8206.2000.tb00429.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
KR 31372 is a benzopyran derivative. Both [H-3]thymidine incorporation and migrations (chemotactic and wound-edge) of cultured smooth muscle cells (SMCs) were greatly stimulated by oxidized low-density lipoprotein (LDL). These effects were significantly suppressed by KR 31372 (10(-7)-10(-6) M) and PDGF-BB antibody (10(-8)-10(-6) M). Preincubation with KR 31372 led to a decrease in the synthesis of PDGF-BB-like immunoreactivity (PDGF-BB-LI) that had been stimulated by oxidized LDL. Otherwise, KR 31372 and probucol strongly inhibited the production of thiobarbituric acid reactive substances (TBARS) caused by the incubation of LDL with Cu2+ ion, and significantly reduced the intracellular oxidative stress when stimulated with H2O2. Taken together, it is suggested that KR 31372 may inhibit the oxidized LDL-stimulated syntheses of DNA and PDGF-BB, and migration of the SMCs, in part, via the antioxidant activity. (C) 2000 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:469 / 476
页数:8
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