拦截性STS 557在狒狒中的进一步报道。

Endokrinologie Pub Date : 1982-07-01
A Komor, N P Goncharov, M Oettel
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引用次数: 0

摘要

每只动物口服sts557 (17 α -氰甲基-17 β -羟基雌二醇-4,9(10)-二烯-3-酮)或左炔诺孕酮,单次剂量0.4 mg。交配6小时后立即进行处理。左炔诺孕酮组30个对照组(18只动物)9例妊娠(30%),26个对照组(17只动物)3例妊娠(11.5%)。在使用STS 557治疗的46个周期(21只动物)中,仅发生1例妊娠(2.2%)(chi - 2检验:与对照周期相比P < 0.01)。因此,STS 557在非人灵长类动物模型中表现出较高的拦截活性。与左炔诺孕酮相比,STS 557没有降低排卵后血浆黄体酮的升高。
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Further report on the interceptive STS 557 in baboons.

STS 557 (17 alpha-cyanomethyl-17 beta-hydroxy-estra-4,9(10)-diene-3-one) or levonorgestrel was given orally as a single dose of 0.4 mg per animal. Treatment was performed immediately after the 6 h mating period. In 30 control cycles (18 animals) 9 pregnancies (30%) and in 26 cycles (17 animals) with levonorgestrel treatment 3 pregnancies (11.5%) were observed. In 46 cycles (21 animals) with STS 557 treatment only one pregnancy (2.2%) occurred (chi 2-test: P less than 0.01 as compared to control cycles). Therefore, STS 557 showed high interceptive activities in this nonhuman primate model. In contrast with levonorgestrel, STS 557 did not decrease the postovulatory rise of plasma progesterone.

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