Zhao X, Zhang Y H, Feng H F
Department of Cardiology, First Teaching Hospital, Third Military Medical College, Chongqing.
Zhonghua Nei Ke Za Zhi. 1990 Aug;29(8):476-8, 510-1.
Sixty patients with coronary artery disease (CAD) were investigated in a randomized, placebo-controlled study. Therapeutic dose of diltiazem markedly inhibited the production of whole blood thromboxane A2(TXA2), but had no effect on the production of prostacyclin(PGI2). Both aspirin 20mg/d and diltiazem plus aspirin had marked inhibitive effects on both TXA2 and PGI2. The order of potency of the three regimens in decreasing TXA2/PGI2 ratio was diltiazem plus aspirin greater than diltiazem greater than aspirin. Diltiazem, aspirin and combination of both all decreased significantly serum lipid peroxides level, but had no effect on serum superoxide dismutase concentration. The results indicate that both therapeutic dose of diltiazem and low-dose of aspirin may modulate TXA2/PGI2 balance and inhibit lipid peroxidation in CAD and that the combination of both drugs may result in best therapeutic effect.
在一项随机、安慰剂对照研究中,对60例冠心病(CAD)患者进行了调查。治疗剂量的地尔硫卓显著抑制全血血栓素A2(TXA2)的产生,但对前列环素(PGI2)的产生没有影响。阿司匹林20mg/d以及地尔硫卓加阿司匹林对TXA2和PGI2均有显著抑制作用。三种治疗方案降低TXA2/PGI2比值的效力顺序为地尔硫卓加阿司匹林大于地尔硫卓大于阿司匹林。地尔硫卓、阿司匹林以及二者联用均显著降低血清脂质过氧化物水平,但对血清超氧化物歧化酶浓度没有影响。结果表明,治疗剂量的地尔硫卓和低剂量阿司匹林均可调节CAD患者的TXA2/PGI2平衡并抑制脂质过氧化,且两种药物联用可能产生最佳治疗效果。