ملخص
Reduced nitric oxide bioavailability caused by endothelial dysfunction or damage is a contributory factor in the initiation and progression of a number of cardiovascular diseases. Delivery of exogenous nitric oxide is an attractive therapeutic option, but current agents lack selectivity for areas of endothelial damage. We tested the hypothesis that a novel nitric oxide donor drug, N-(S-nitroso-N-acetylpenicillamine)-2-amino-2-deoxy-1,3,4,6-tetra-O-acet yl-P-glucopyranose [RIG200], which has selective effects in endothelium-denuded isolated arteries in vitro, would exert similar effects in dorsal hand veins with experimentally damaged endothelium in vivo.
| اللغة الأصلية | English |
|---|---|
| الصفحات (من إلى) | 75-81 |
| عدد الصفحات | 7 |
| دورية | Clinical Pharmacology and Therapeutics |
| مستوى الصوت | 68 |
| رقم الإصدار | 1 |
| المعرِّفات الرقمية للأشياء | |
| حالة النشر | Published - 2000 |