Toppozada M, El-Sokkary H, El-Abd M, El-Fazary A, El-Rahman H A
Prostaglandins Med. 1981 Feb;6(2):203-11. doi: 10.1016/0161-4630(81)90090-2.
Previous data in the human generally indicate that therapeutic doses of prostaglandins (PGs) are not luteolytic. In an attempt to evaluate whether a high dose infusion (approx. 5 microgram/min for 6 hours) of a potent PG (15-methyl PGF2 alph) analogue is luteolytic, 15-methyl PGF2 alpha was administrated in the mid-luteal phase of 10 normally menstruating volunteers. The infusion induced a significant and sustained luteolytic response in 8 subjects as evidenced by a drop in progesterone levels and premature menstrual-like bleeding. In the other two cases luteal recovery was apparent from the regained normal plasma levels of progesterone and a normal cycle length. Thus, it can be concluded that luteolysis can be induced in humans by this PG provided that high dose infusions are utilized which also cause a lot of undesirable side-effects.
以往在人体中的数据一般表明,治疗剂量的前列腺素(PGs)不会引起黄体溶解。为了评估高剂量输注(约5微克/分钟,持续6小时)一种强效PG(15-甲基PGF2α)类似物是否会引起黄体溶解,在10名正常月经周期的志愿者的黄体中期给予15-甲基PGF2α。输注导致8名受试者出现显著且持续的黄体溶解反应,这可通过孕酮水平下降和类似月经提前出血得以证明。在另外两例中,从孕酮血浆水平恢复正常和月经周期长度正常可明显看出黄体恢复。因此,可以得出结论,只要使用高剂量输注,这种PG就能在人体中诱导黄体溶解,而高剂量输注也会引起许多不良副作用。