De La Cruz J P, Cámara S, Frutos M A, Sánchez De La Cuesta F
Department of Pharmacology and Therapeutics, School of Medicine, University of Málaga, Spain.
Eur J Clin Pharmacol. 1992;43(3):307-9. doi: 10.1007/BF02333029.
The antiproteinuric effect of the antiplatelet agent dipyridamole has been assessed after inhibition of thromboxane B2 (TxB2) synthesis in 8 patients with confirmed membranous glomerulonephritis. There were three study periods, each of 30 days, and 45 days apart, namely a washout period, treatment with dipyridamole 300 mg/d, and dipyridamole 225 mg/d plus aspirin 150 mg/d. On Days 1 and 30 of each study period serum and urine creatinine, 24-h excretion of protein, creatinine clearance, platelet aggregometry on whole blood and serum TxB2 were measured. Treatment with dipyridamole alone or with aspirin produced significant inhibition of platelet aggregation and a fall in 24-h protein excretion; the latter amounted to 54% with dipyridamole alone and 56% with dipyridamole plus aspirin (NS). Dipyridamole plus aspirin caused an 82% reduction in serum TxB2.
在8例确诊为膜性肾小球肾炎的患者中,抑制血栓素B2(TxB2)合成后,评估了抗血小板药物双嘧达莫的抗蛋白尿作用。研究分为三个阶段,每个阶段30天,间隔45天,分别为洗脱期、双嘧达莫300mg/d治疗期、双嘧达莫225mg/d加阿司匹林150mg/d治疗期。在每个研究阶段的第1天和第30天,测量血清和尿肌酐、24小时蛋白排泄量、肌酐清除率、全血血小板聚集率和血清TxB2。单独使用双嘧达莫或与阿司匹林联合治疗均能显著抑制血小板聚集,并使24小时蛋白排泄量下降;单独使用双嘧达莫时下降了54%,双嘧达莫加阿司匹林时下降了56%(无显著性差异)。双嘧达莫加阿司匹林使血清TxB2降低了82%。