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[11-脱氧前列腺素E1合成类似物的促黄体生成和溶黄体特性]

[The luteotropic and luteolytic properties of synthetic analogs of 11-deoxy-PGE1].

作者信息

Saitova M Iu, Bagaeva S G, Zarudiĭ F S, Lazareva D N, Davydova V A

出版信息

Farmakol Toksikol. 1990 Nov-Dec;53(6):27-31.

PMID:2081563
Abstract

The luteotropic and luteolytic properties of synthetic analogues of 11-desoxy-PGE1 were studied. Compounds Nos. 1 and 2 depending on the dose exerted the opposite effect: in low doses--luteotropic, in high doses--luteolytic. Compounds Nos. 3, 4 and 5 in the whole range of doses exhibited only luteolytic properties. The ranges of doses of prostaglandin exerting the luteotropic effect depend on the structural modifications of prostaglandin molecule. The luteolytic effect of synthetic analogue No. 5 was suggested to be determined by its influence on the hypophysis through the change of contents of cyclic nucleotides and gonadotropic hormones. It was demonstrated that the luteolytic effect of compound No. 5 is realized through the central nervous system, in particular, through the hypophysis.

摘要

研究了11-脱氧-PGE1合成类似物的促黄体生成和溶黄体特性。化合物1号和2号根据剂量产生相反的作用:低剂量时为促黄体生成作用,高剂量时为溶黄体作用。化合物3号、4号和5号在整个剂量范围内仅表现出溶黄体特性。发挥促黄体生成作用的前列腺素剂量范围取决于前列腺素分子的结构修饰。有人认为合成类似物5号的溶黄体作用是通过环核苷酸和促性腺激素含量的变化对垂体的影响来决定的。已证明化合物5号的溶黄体作用是通过中枢神经系统,特别是通过垂体实现的。

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