Pulkkinen M O, Piiroinen O, Vainikka J
Department of Obstetrics and Gynecology, University of Turku, Finland.
Arch Gynecol Obstet. 1989;244(2):75-8. doi: 10.1007/BF00931376.
In the 72 h after a single oral dose of 400 mg of the antiprogesterone mifepristone, 12 out of 14 first and one second trimester fetuses had a slight increase in heart rate; 2 fetuses died and one aborted. During the same 72 h, uterine activity increased moderately, and was physiological with no increase in resting pressure. The treatment sensitized the uterus to prostaglandin (PG) about ten-fold. A low, 0.05 mg IM, dose of sulprostone caused the demise of 5 more fetuses and caused the onset of clinical abortion in less than 2 h. After a relatively short hypertonic phase uterine resting pressure fell to normal levels and active contractions occurred leading to expulsion of uterine contents. The plasma level of progesterone (P) remained unaltered after mifepristone treatment, but the levels of estradiol 17b (E2) and cortisol increased. The plasma level of mifepristone was 1640 +/- 424 ng. ml -1 at 72 h, and the substance was still detectable after one week.
单次口服400毫克抗孕激素米非司酮后的72小时内,14例孕早期胎儿中的12例以及1例孕中期胎儿心率略有增加;2例胎儿死亡,1例流产。在同一72小时内,子宫活动适度增加,为生理性增加,静息压力未升高。该治疗使子宫对前列腺素(PG)的敏感性提高了约10倍。低剂量(0.05毫克,肌肉注射)的硫前列酮导致另外5例胎儿死亡,并在不到2小时内引发临床流产。经过相对较短的高张期后,子宫静息压力降至正常水平,并出现主动收缩,导致子宫内容物排出。米非司酮治疗后孕酮(P)的血浆水平保持不变,但雌二醇17β(E2)和皮质醇水平升高。72小时时米非司酮的血浆水平为1640±424纳克·毫升-1,一周后仍可检测到该物质。