Williams M T, Roth M S, Marsh J M, LeMaire W J
J Clin Endocrinol Metab. 1979 Mar;48(3):437-40. doi: 10.1210/jcem-48-3-437.
The purpose of this study was to determine whether estrogens exerted a direct inhibitory effect on progesterone synthesis in isolated human luteal cells in vitro. It was found that hCG stimulated progesterone synthesis by luteal cells, obtained from corpora lutea of the menstrual cycle, whereas cells isolated from corpora lutea of pregnancy were unresponsive to exogenous hCG. Estradiol markedly inhibited (P less than 0.001) this hCG effect in luteal cells of the menstrual cycle, and this inhibition was dose dependent. Estradiol did not block the stimulation of cAMP accumulated by hCG in the luteal cells of the cycle but did inhibit the stimulatory effect of dibutyryl cAMP on progesterone synthesis. These data suggest that estrogens may directly cause functional luteolysis in the human and that its site of action may be after the accumulation of cAMP.
本研究的目的是确定雌激素在体外对分离出的人黄体细胞孕酮合成是否具有直接抑制作用。研究发现,人绒毛膜促性腺激素(hCG)可刺激从月经周期黄体获取的黄体细胞合成孕酮,而从妊娠黄体分离出的细胞对外源性hCG无反应。雌二醇显著抑制(P<0.001)月经周期黄体细胞的这种hCG效应,且这种抑制呈剂量依赖性。雌二醇并未阻断hCG在周期黄体细胞中积累cAMP的刺激作用,但确实抑制了二丁酰cAMP对孕酮合成的刺激作用。这些数据表明,雌激素可能直接导致人体功能性黄体溶解,其作用位点可能在cAMP积累之后。