Check J H, Adelson H G
UMONJ, Robert Wood Johnson Medical School, Camden.
Int J Fertil. 1990 Nov-Dec;35(6):343-6.
Leuprolide acetate was used to suppress the endogenous gonadotropins in order to prevent premature luteinization in two women under ovulation induction therapy. One patient had previously developed premature luteinization with clomiphene citrate, but consistently produced only one mature follicle with hMG therapy. However, when leuprolide acetate was started prior to hMG during an attempt for in vitro fertilization, it failed to stimulate even a mild rise in her serum estradiol. The other patient, who was not able to make a mature follicle with hMG alone because of premature luteinization, was enabled to make mature follicles with leuprolide therapy alone (without hMG). The exact mechanism for these totally different responses to leuprolide acetate in two perimenopausal women is not known.
醋酸亮丙瑞林被用于抑制内源性促性腺激素,以防止两名接受促排卵治疗的女性发生过早黄素化。一名患者此前使用枸橼酸氯米芬时出现过早黄素化,但使用人绝经期促性腺激素(hMG)治疗时始终仅产生一个成熟卵泡。然而,在一次体外受精尝试中,当在hMG治疗前开始使用醋酸亮丙瑞林时,甚至未能刺激她的血清雌二醇出现轻度升高。另一名患者因过早黄素化单独使用hMG无法形成成熟卵泡,而单独使用亮丙瑞林治疗(不使用hMG)则能够形成成熟卵泡。两名围绝经期女性对醋酸亮丙瑞林产生这些完全不同反应的确切机制尚不清楚。