Koper J W, Molijn G J, van Uffelen C J, Stigter E, Lamberts S W
Department of Internal Medicine III, Erasmus University Rotterdam, The Netherlands.
Life Sci. 1997;60(9):617-24. doi: 10.1016/s0024-3205(96)00698-4.
The antiglucocorticoid action of the antiprogestin RU 38486 has interfered with its successful clinical application in long-term treatment. Several new antiprogestins (Org 31710, Org 31806 and ZK 98299) have recently been developed with the aim to eliminate this side-effect. We have used a human lymphocyte proliferation assay to estimate the antiglucocorticoid potency of RU 38486 and the newer antiprogestins. In this assay 100 nmol/L RU 38486 shifted the dexamethasone inhibition curve by at least one order of magnitude. The other antiprogestins showed no effect at 100 nmol/L. RU 38486 (30 nmol/L) was able to antagonize 1000 nmol/L dexamethasone. The other antiprogestins showed only slight effects even at 1000 nmol/L. We conclude that the new antiprogestins have antiglucocorticoid effects that are one to two orders of magnitude lower than that of RU 38486. This may make them more suitable than RU 38486 for application in long-term antiprogestin treatment.
抗孕激素RU 38486的抗糖皮质激素作用妨碍了其在长期治疗中的成功临床应用。最近已研发出几种新型抗孕激素(Org 31710、Org 31806和ZK 98299),旨在消除这种副作用。我们使用人淋巴细胞增殖试验来评估RU 38486和新型抗孕激素的抗糖皮质激素效力。在该试验中,100 nmol/L的RU 38486使地塞米松抑制曲线至少偏移一个数量级。其他抗孕激素在100 nmol/L时无作用。30 nmol/L的RU 38486能够拮抗1000 nmol/L的地塞米松。其他抗孕激素即使在1000 nmol/L时也仅显示出轻微作用。我们得出结论,新型抗孕激素的抗糖皮质激素作用比RU 38486低一至两个数量级。这可能使它们比RU 38486更适合用于长期抗孕激素治疗。