Siebers J W, Wuttke W, Engel W
Acta Endocrinol (Copenh). 1977 Sep;86(1):173-9. doi: 10.1530/acta.0.0860173.
During pregnancy, binding of 125I-labelled HCG to the rat ovary increases markedly from the 3rd to the 17th day of pregnancy but is reduced drastically at the end of pregnancy and after delivery. At the 17th day of pregnancy the HCG-binding capacity of the rat ovary is raised 76-fold in comparison to oestrous rats (17th day of pregnancy: 128 X 10(-15) mol/mg wet weight; oestrus: 1.67 X 10(-15) mol/mg wet weight). It is assumed that only LH receptors not occupied by endogenous hormone are covered by our assay. The high number of "free" ovarian HCG receptors during pregnancy apparently represents "Spare" receptors, the functional significance of which remains unclear. It is suggested that the metabolic activity of the ovarian luteal cells during pregnancy is not restricted by the number of HCG receptors present, but through the level of the endogenous gonadotrophic hormone and/or some unknown factors residing in the luteal cell.
在怀孕期间,125I标记的人绒毛膜促性腺激素(HCG)与大鼠卵巢的结合在妊娠第3天到第17天显著增加,但在妊娠末期和分娩后急剧下降。与发情期大鼠相比,妊娠第17天时大鼠卵巢的HCG结合能力提高了76倍(妊娠第17天:128×10⁻¹⁵摩尔/毫克湿重;发情期:1.67×10⁻¹⁵摩尔/毫克湿重)。据推测,我们的检测方法仅覆盖未被内源性激素占据的促黄体生成素(LH)受体。怀孕期间卵巢中大量的“游离”HCG受体显然代表“备用”受体,其功能意义尚不清楚。有人提出,怀孕期间卵巢黄体细胞的代谢活性不受现有HCG受体数量的限制,而是受内源性促性腺激素水平和/或黄体细胞中某些未知因素的影响。