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Ro 44-9883,一种新型非肽类糖蛋白IIb-糖蛋白IIIa拮抗剂,可防止豚鼠体外循环模型中的血小板损失。

Ro 44-9883, a new non-peptidic GPIIb-GPIIIa antagonist prevents platelet loss in a guinea pig model of extracorporeal circulation.

作者信息

Carteaux J P, Steiner B, Roux S

机构信息

Pharma Division, Hoffmann-La Roche Ltd, Basel, Switzerland.

出版信息

Thromb Haemost. 1993 Nov 15;70(5):817-21.

PMID:8128440
Abstract

Extensive contact between blood and artificial surfaces causes platelet activation and depletion. The aim of the present study was to test the efficacy of Ro 44-9883, a potent and selective peptidomimetic GPIIb-IIIa antagonist, in preventing platelet loss in guinea pigs undergoing extracorporeal circulation (ECC) with bubble oxygenation. In 15 guinea pigs, an arterio-arterial shunt was created and perfused for 1 h from the aortic arch to the descending aorta. The guinea pigs were divided into three groups: A control group receiving only heparin as an i.v. bolus, a low dose-treated group and a high dose-treated group receiving in addition to heparin and before starting ECC, 1 or 7 mg/kg Ro 44-9883 as an i.v. bolus, respectively. In the control group, the platelet count at 30 and 60 min of ECC was dramatically decreased (35 +/- 4% and 25 +/- 3% of initial value). In the low dose-treated group, Ro 44-9883 partially prevented the drop in platelet count (69 +/- 8% and 54 +/- 9%; p < 0.05) whereas in the high dose-treated group, the platelet count was normal at 30 min (97 +/- 8%) and only slightly decreased at 60 min (80 +/- 7%). Mean arterial pressure and hematocrit were not significantly different between groups during the experiment. We conclude that i) ECC in guinea pigs provides an interesting in-vivo model for studying platelet loss by contact activation and ii) Ro 44-9883 prevents platelet loss during ECC in a dose dependent manner.

摘要

血液与人工表面的广泛接触会导致血小板活化和消耗。本研究的目的是测试一种强效且选择性的肽模拟物GPIIb-IIIa拮抗剂Ro 44-9883在预防豚鼠体外循环(ECC)气泡氧合过程中血小板损失方面的疗效。在15只豚鼠中,建立了动脉-动脉分流,并从主动脉弓到降主动脉灌注1小时。豚鼠被分为三组:对照组仅静脉推注肝素;低剂量治疗组和高剂量治疗组,除肝素外,在开始ECC前分别静脉推注1或7 mg/kg Ro 44-9883。在对照组中,ECC 30分钟和60分钟时血小板计数显著下降(分别为初始值的35±4%和25±3%)。在低剂量治疗组中,Ro 44-9883部分预防了血小板计数的下降(分别为69±8%和54±9%;p<0.05),而在高剂量治疗组中,30分钟时血小板计数正常(97±8%),60分钟时仅略有下降(80±7%)。实验期间各组间平均动脉压和血细胞比容无显著差异。我们得出结论:i)豚鼠的ECC为研究接触激活导致的血小板损失提供了一个有趣的体内模型;ii)Ro 44-9883以剂量依赖的方式预防ECC期间的血小板损失。

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