YC-1, a benzyl indazole derivative, stimulates vascular cGMP and inhibits neointima formation

被引:38
作者
Tulis, DA [1 ]
Durante, W
Peyton, KJ
Chapman, GB
Evans, AJ
Schafer, AI
机构
[1] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pharmacol, Houston, TX 77030 USA
[3] Vet Affairs Med Ctr, Houston, TX 77030 USA
关键词
YC-1; balloon angioplasty; stenosis; neointima;
D O I
10.1006/bbrc.2000.3942
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The pathobiologic process of arterial stenosis following balloon angioplasty continues to be an enigmatic problem in clinical settings. This research project investigates the ability of YC-1, a benzyl indazole derivative that sensitizes sGC/cGMP, to stimulate endogenous cGMP and attenuate balloon injury-induced neointima (NI) formation in the rat carotid artery. Northern and Western blot analyses revealed enhanced acute expression of iNOS and inducible heme oxygenase (HO-1) mRNA and protein in the injured artery. The contralateral uninjured artery also demonstrated acute HO-1 mRNA and protein induction without detectable iNOS expression. Perivascular application of YC-1 immediately following injury significantly stimulated acute vessel wall cGMP compared to untreated controls. YC-1 treated sections demonstrated significant reduction in NI area (-74%), NI area/medial wall area (-72%), and NI thickness (-76%) 2 weeks post-injury. These results directly implicate YC-1 as a potent new therapeutic agent capable of reducing post-angioplasty stenosis through endogenous CO- and/or NO-mediated, cGMP-dependent processes. (C) 2000 Academic Press.
引用
收藏
页码:646 / 652
页数:7
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