杨波, 曹霖, 方瑞英, 顾芝萍. 抗孕唑对假孕大鼠的溶黄体作用J. 药学学报, 1999, 34(5): 321-324.
引用本文: 杨波, 曹霖, 方瑞英, 顾芝萍. 抗孕唑对假孕大鼠的溶黄体作用J. 药学学报, 1999, 34(5): 321-324.
Cao Lin , Gu Zhiping, Yang Bo Fang Ruiying, . LUTEOLYTIC EFFECT OF DL111-IT IN PSEUDOPREGNANT RATSJ. Acta Pharmaceutica Sinica, 1999, 34(5): 321-324.
Citation: Cao Lin , Gu Zhiping, Yang Bo Fang Ruiying, . LUTEOLYTIC EFFECT OF DL111-IT IN PSEUDOPREGNANT RATSJ. Acta Pharmaceutica Sinica, 1999, 34(5): 321-324.

抗孕唑对假孕大鼠的溶黄体作用

LUTEOLYTIC EFFECT OF DL111-IT IN PSEUDOPREGNANT RATS

  • 摘要: 目的:测定抗孕唑对假孕大鼠黄体和蜕膜的作用,以探索抗孕唑抗早孕作用的机制。方法:用放射免疫法和紫外分光光度计等方法。结果:抗孕唑可缩短大鼠假孕期4.8 d;降低卵巢重量,蛋白含量和血清孕酮浓度;给药5 d后,3β-HSD活性显著低于对照组;20α-HSD的活性则在给药1 d后即非常显著上升;子宫PGF含量也显著升高,而给药5 d后,子宫和血清中的PGF分别为对照组的3.2倍和2.2倍。结论:抗孕唑的溶黄体作用是由于降低假孕大鼠血清孕酮水平和增加PGF含量所致,似乎与胚胎坏死无关。

     

    Abstract: AIM:To observe the luteolytic effects of DL111-IT in pseudopregnant rats. METHODS:Radioimmunoassay was used to estimate serum progesterone concentration and PGF content in uterus and serum; the activities of 3β-HSD and 20α-HSD in ovaries were assayed spectrophotometrically. RESULTS:DL111-IT was shown to shorten normal pseudopregnant period of rats by 4.8 days and decrease ovarian fresh weight, protein content and serum progesterone level dramatically. After im DL111-IT for 5 d, activities of 3β-HSD of pseudopregnant rats decreased 53.8%, while that of 20α-HSD incresed significantly after only one injection of DL111-IT (control: 1.0±0.4 mu.mg-1 protein; treatment: 6.9±1.8 mu.mg-1 protein); PGF concentration in uterus and serum of pseudopregnant rats increased 40.1% and 36.5%, respectively. CONCLUSION:DL111-IT induced luteolysis in pseudopregnant rats.

     

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