Hermán F, Malomvölgyi B, Hadházy P, Magyar K
Department of Pharmacodynamics, Semmelweis University of Medicine, Budapest, Hungary.
Biomed Biochim Acta. 1988;47(10-11):S113-6.
Chinoin-7284 and Chinoin-7384 are chemically stable derivatives of prostacyclin. We compared the hypotensive and antiaggregatory effects of PGI2 and the two analogues using our computerized aggregometric system. The in vivo antiaggregatory activity was measured with a modified filtration pressure technique in anaesthetized beagle dogs: The change in arterial blood pressure was measured simultaneously. The dose-response relationship and the duration of action of prostacyclin and their analogues following bolus administration have been determined. The molar dose of PGI2, CH-7284 and CH-7384 that produced 25 mmHg reduction in filtration pressure were 0.3 +/- 0.06 nmol/kg; 7.37 +/- 0.94 nmol/kg; 17.19 +/- 1.76 nmol/kg respectively (n = 6). The molar doses that produced the same decrease in mean arterial pressure were 0.61 +/- 0.06 nmol/kg; 15.59 +/- 4.73 nmol/kg; 21.05 +/- 7.20 nmol/kg respectively (n = 6). There were no significant differences between equipotent doses of prostacyclin and its analogues with respect to the duration of antiaggregatory and hypotensive action. The in vivo selectivity ratios (hypotensive potency/antiaggregatory potency) of PGI2, CH-7284 and CH-7384 were 0.49, 0.47 and 0.85 respectively. The results indicate that these two PGI2 analogues have the same character as regards the in vivo duration of actions and in vivo selectivity, as has the parent compound.
奇诺因 -7284 和奇诺因 -7384 是前列环素的化学稳定衍生物。我们使用计算机化凝集测定系统比较了前列环素(PGI2)和这两种类似物的降压及抗聚集作用。在麻醉的比格犬中,采用改良的滤过压技术测量体内抗聚集活性,同时测量动脉血压变化。确定了推注给药后前列环素及其类似物的剂量 - 反应关系和作用持续时间。使滤过压降低 25 mmHg 的 PGI2、CH -7284 和 CH -7384 的摩尔剂量分别为 0.3±0.06 nmol/kg、7.37±0.94 nmol/kg、17.19±1.76 nmol/kg(n = 6)。使平均动脉压产生相同降低的摩尔剂量分别为 0.61±0.06 nmol/kg、15.59±4.73 nmol/kg、21.05±7.20 nmol/kg(n = 6)。在等效剂量下,前列环素及其类似物在抗聚集和降压作用持续时间方面无显著差异。PGI2、CH -7284 和 CH -7384 的体内选择性比率(降压效力/抗聚集效力)分别为 0.49、0.47 和 0.85。结果表明,这两种 PGI2 类似物在体内作用持续时间和体内选择性方面与母体化合物具有相同的特性。