Montz F J, Wolff A J, Gambone J C
Department of Obstetrics and Gynecology, University of California, Los Angeles 90024-1740.
Cancer Res. 1991 Apr 15;51(8):2124-6.
Premature ovarian failure and reduced fecundity are well-documented consequences of cytotoxic chemotherapy used to treat patients with malignant diseases. To investigate the ability of different hormonal agents to block the effects of cyclophosphamide (CTX) on reproductive function, sexually mature female Long-Evans rats were studied. Model development demonstrated that CTX, 6 mg/kg/day, 5 days/week for 3 weeks, was successful at inducing acyclicity and significantly reducing fertility and fecundity, with acceptable mortality, when compared to higher/lower dosages. Utilizing this model, animals were treated with CTX in combination with an inert vehicle, Lupron, 80 micrograms/kg every 24 h, Lupron, 40 micrograms/kg every 12 h, or s.c. progesterone capsules obtaining serum progesterone levels of 20-30 ng/ml. We concluded that progesterone was able to protect the gonad from the negative effects of CTX, maintaining fertility and fecundity rates not significantly different from those of untreated control animals. Lupron given every 12 h had a similar effect on fertility, but failed to protect fecundity (P less than 0.001).
卵巢早衰和生育力降低是用于治疗恶性疾病患者的细胞毒性化疗的有据可查的后果。为了研究不同激素制剂阻断环磷酰胺(CTX)对生殖功能影响的能力,对性成熟的雌性Long-Evans大鼠进行了研究。模型建立表明,与更高/更低剂量相比,CTX以6mg/kg/天、每周5天、共3周的剂量成功诱导无排卵,并显著降低生育力和繁殖力,且死亡率可接受。利用该模型,动物分别接受CTX与惰性赋形剂、每24小时80微克/千克的亮丙瑞林、每12小时40微克/千克的亮丙瑞林或皮下注射孕酮胶囊(使血清孕酮水平达到20-30纳克/毫升)联合治疗。我们得出结论,孕酮能够保护性腺免受CTX的负面影响,使生育力和繁殖力维持在与未治疗的对照动物无显著差异的水平。每12小时给予亮丙瑞林对生育力有类似影响,但未能保护繁殖力(P<0.001)。