Laboratory of Neuroendocrinology, GIGA Neurosciences, University of Liège, Liège, Belgium.
Institute of Metabolic and Cardiovascular Diseases (I2MC) Equipe 4, Inserm U1297-UPS, CHU, Toulouse 31432, France.
eNeuro. 2024 Oct 23;11(10). doi: 10.1523/ENEURO.0271-23.2024. Print 2024 Oct.
Estrogens act through nuclear and membrane-initiated signaling. Estrogen receptor alpha (ERα) is critical for reproduction, but the relative contribution of its nuclear and membrane signaling to the central regulation of reproduction is unclear. To address this question, two complementary approaches were used: estetrol (E) a natural estrogen acting as an agonist of nuclear ERs, but as an antagonist of their membrane fraction, and the C451A-ERα mouse lacking mERα. E dose- dependently blocks ovulation in female rats, but the central mechanism underlying this effect is unknown. To determine whether E acts centrally to control ovulation, its effect was tested on the positive feedback of estradiol (E) on neural circuits underlying luteinizing hormone (LH) secretion. In ovariectomized females chronically exposed to a low dose of E, estradiol benzoate (EB) alone or combined with progesterone (P) induced an increase in the number of kisspeptin (Kp) and gonadotropin-releasing hormone (GnRH) neurons coexpressing Fos, a marker of neuronal activation. E blocked these effects of EB, but not when combined to P. These results indicate that E blocked the central induction of the positive feedback in the absence of P, suggesting an antagonistic effect of E on mERα in the brain as shown in peripheral tissues. In parallel, as opposed to wild-type females, C451A-ERα females did not show the activation of Kp and GnRH neurons in response to EB unless they are treated with P. Together these effects support a role for membrane-initiated estrogen signaling in the activation of the circuit mediating the LH surge.
雌激素通过核和膜起始信号转导发挥作用。雌激素受体 α (ERα) 对生殖至关重要,但它的核和膜信号转导对生殖的中枢调节的相对贡献尚不清楚。为了解决这个问题,采用了两种互补的方法:雌三醇(E)是一种天然雌激素,作为核 ERs 的激动剂,但作为其膜部分的拮抗剂,以及缺乏 mERα 的 C451A-ERα 小鼠。E 剂量依赖性地阻断雌性大鼠的排卵,但这种作用的中枢机制尚不清楚。为了确定 E 是否通过中枢作用来控制排卵,测试了它对黄体生成素 (LH) 分泌神经回路的雌二醇 (E) 正反馈的影响。在长期暴露于低剂量 E 的去卵巢雌性动物中,苯甲酸雌二醇 (EB) 单独或与孕激素 (P) 联合诱导 kisspeptin (Kp) 和促性腺激素释放激素 (GnRH) 神经元的数量增加,这些神经元共表达 Fos,这是神经元激活的标志物。E 阻断了这些 EB 的作用,但与 P 联合时则不会。这些结果表明,E 在没有 P 的情况下阻断了中枢诱导的正反馈,表明 E 在大脑中的 mERα 上具有拮抗作用,正如在外周组织中所显示的那样。与此同时,与野生型雌性动物相反,C451A-ERα 雌性动物在没有 P 治疗的情况下不会对 EB 产生反应,从而激活 Kp 和 GnRH 神经元。这些效应共同支持膜起始雌激素信号在激活介导 LH 激增的回路中的作用。