INHIBITION OF PLATELET ACTIVITY BY S-NITROSOGLUTATHIONE DURING CORONARY ANGIOPLASTY

被引:178
作者
LANGFORD, EJ
BROWN, AS
WAINWRIGHT, RJ
DEBELDER, AJ
THOMAS, MR
SMITH, REA
RADOMSKI, MW
MARTIN, JF
MONCADA, S
机构
[1] UNIV LONDON KINGS COLL,SCH MED & DENT,DEPT MED,LONDON SE5 9PJ,ENGLAND
[2] UNIV LONDON KINGS COLL HOSP,DEPT CARDIOL,LONDON,ENGLAND
[3] WELLCOME RES LABS,BECKENHAM BR3 3BS,KENT,ENGLAND
关键词
D O I
10.1016/S0140-6736(94)90287-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Platelet activation is associated with acute vessel occlusion and chronic restenosis after percutaneous transluminal coronary angioplasty (PTCA), Organic nitrates, which act by releasing the vasodilator and anti-platelet agent nitric oxide (NO), have a predominantly vasodilator action and cause hypotension at doses required to inhibit platelet activation. S-nitrosoglutathione (GSNO) is an NO donor with a preferential action on platelets. We investigated platelet activation in patients undergoing PTCA and the effect of GSNO. Blood was sampled from the coronary sinus to measure platelet surface expression of P-selectin and glycoprotein IIb/IIIa as indices of platelet activation. In 7 control patients, PTCA caused a rise in platelet surface expression of P-selectin and glycoprotein IIb/IIIa, which was maximal 5 minutes after PTCA, indicating increased platelet activation despite treatment with aspirin, glyceryl trinitrate, and heparin. 6 patients received an intracoronary infusion of GSNO, starting 10 min before PTCA. GSNO significantly inhibited the PTCA-induced increase in platelet surface expression of P-selectin and glycoprotein IIb/IIIa without altering blood pressure. These findings show that platelets are activated following PTCA and that GSNO can prevent this activation.
引用
收藏
页码:1458 / 1460
页数:3
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