Löbel P, Schrör E, Schrör K
Institut für Pharmakologie, Universität Düsseldorf, F.R.G.
Biomed Biochim Acta. 1988;47(10-11):S86-9.
The effect of a thromboxane receptor antagonist (Daltroban, BM 13.505) on platelet function, vascular PGI2 formation and the severity of atherosclerotic lesions was studied in rabbits, fed for 4 months a cholesterol rich (1%) diet. Daltroban (10 mg/kg x day) significantly antagonized the hypercholesterolemia induced enhanced platelet aggregability, thromboxane formation and ATP secretion. The vascular PGI2 biosynthesis ("basal" or bradykinin stimulated), the number of PGI2 receptors on platelet membranes and the atherosclerotic plaque formation in the aorta were not affected by Daltroban. We suggest that in addition to a reduction of platelet hyperreactivity, protection of the vessel wall appears to be required for prevention of atherosclerosis in this model.
研究了血栓素受体拮抗剂(达曲班,BM 13.505)对喂食富含1%胆固醇饮食4个月的家兔血小板功能、血管前列环素(PGI2)生成及动脉粥样硬化病变严重程度的影响。达曲班(10毫克/千克/天)显著拮抗了高胆固醇血症诱导的血小板聚集性增强、血栓素生成及ATP分泌。血管PGI2生物合成(“基础”或缓激肽刺激的)、血小板膜上PGI2受体数量及主动脉粥样硬化斑块形成均未受达曲班影响。我们认为,在此模型中,除降低血小板高反应性外,预防动脉粥样硬化似乎还需要保护血管壁。