Dumesic D A, Goldsmith P C, Jaffe R B
Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco 94143.
J Clin Endocrinol Metab. 1987 Dec;65(6):1147-53. doi: 10.1210/jcem-65-6-1147.
In adult women, estradiol (E2) sensitizes the pituitary to GnRH. To assess whether this effect develops during intrauterine life, dispersed pituitary cells from second trimester male and female fetuses were cultured on extracellular matrix-coated plates. E2 (10(-8) mol/L) exposure for 72 h resulted in a significant increase in LH release when cells were stimulated with GnRH and caused a significant shift to the left of the dose-response curve for GnRH-stimulated LH release [relative potency ratio, 0.33 +/- 0.05 (+/- SE)]. E2-enhanced LH release was not associated with an increase in cell number, total LH content, or percentage of LH-containing cells (immunocytochemistry). The EC50 of GnRH-stimulated LH release and the degree of E2 sensitization were not sex dependent, although female fetal pituitary cells in the absence of E2 had significantly greater LH content and released more LH under basal and GnRH-stimulated conditions than cells from male fetuses. Therefore, E2 sensitization of second trimester human fetal gonadotrophs to GnRH does occur, is not influenced by sex, and may involve an acutely releasable LH pool. At these gestational ages, basal and maximal GnRH-stimulated LH release as well as total LH content are greater in the female than the male. Thus, E2 sensitization of GnRH responsiveness appears to have its origins during intrauterine fetal life.
在成年女性中,雌二醇(E2)使垂体对促性腺激素释放激素(GnRH)敏感。为了评估这种作用是否在子宫内生活期间就已形成,将来自妊娠中期雄性和雌性胎儿的分散垂体细胞培养在细胞外基质包被的培养板上。当用GnRH刺激细胞时,暴露于E2(10^(-8) mol/L)72小时导致促黄体生成素(LH)释放显著增加,并使GnRH刺激的LH释放剂量反应曲线显著左移[相对效价比,0.33±0.05(±标准误)]。E2增强的LH释放与细胞数量、总LH含量或含LH细胞百分比的增加无关(免疫细胞化学)。GnRH刺激的LH释放的半数有效浓度(EC50)和E2致敏程度不依赖于性别,尽管在没有E2的情况下,雌性胎儿垂体细胞的LH含量显著高于雄性胎儿的细胞,并且在基础和GnRH刺激条件下释放的LH更多。因此,妊娠中期人类胎儿促性腺激素细胞对GnRH的E2致敏作用确实存在,不受性别的影响,并且可能涉及一个可急性释放的LH池。在这些胎龄时,雌性的基础和最大GnRH刺激的LH释放以及总LH含量均高于雄性。因此,GnRH反应性的E2致敏作用似乎起源于子宫内胎儿期。