Richter T A, Robinson J E, Lozano J M, Evans N P
Laboratory of Neuroendocrinology, The Babraham Institute, Cambridge, UK.
J Neuroendocrinol. 2005 Mar;17(3):161-9. doi: 10.1111/j.1365-2826.2005.01287.x.
Elevated oestradiol concentrations during the follicular phase stimulate a surge in gonadotropin-releasing hormone (GnRH) and luteinising hormone (LH) concentrations, which leads to ovulation. Progesterone can block the oestradiol-induced GnRH/LH surge, but the mechanism that is involved is unclear. We examined the effect of progesterone on oestradiol-induced activation of cells within the ovine hypothalamus/preoptic area (POA) to determine: (i) in which regions progesterone acts to block the GnRH/LH surge and (ii) whether progesterone directly or indirectly prevents activation of oestradiol-responsive cells. Cellular activation was assessed by measuring the number of cells that expressed Fos (an immediate early gene). Exposure to increased oestradiol concentrations in the absence of progesterone (which normally stimulates a LH surge) did not cause any region-specific changes in hypothalamic Fos expression during the activation stage of the LH surge-induction process (Experiment 1). The same treatment significantly increased cellular activation within the POA, lateral septum (LS), and arcuate nucleus at the time of surge onset (Experiment 2). Concurrent exposure to increased oestradiol and progesterone concentrations during the activation stage of the surge-induction process (which normally blocks the LH surge) was associated with significantly reduced cellular activation within the ventromedial hypothalamus and anterior hypothalamic area, relative to the positive controls (oestradiol increment alone) and arcuate nucleus relative to the negative controls (no increment in oestradiol) during the activation stage (Experiment 1). At the time of surge onset (Experiment 2), exposure to progesterone during the activation period prevented the oestradiol-induced increase in cellular activation that occurred in the POA, LS and arcuate nucleus of the positive controls. These results demonstrated that oestradiol and progesterone induced differential region- and time-specific effects on cellular activation within the regions of the ovine brain that generate the preovulatory GnRH/LH surge. Moreover, the lack of cellular activation within the POA, LS and arcuate nucleus at the time of surge onset in animals exposed to progesterone during the activation stage is consistent with the hypothesis that progesterone can block the preovulatory surge by direct inhibition of oestradiol-induced cellular activation in these areas.
卵泡期雌二醇浓度升高会刺激促性腺激素释放激素(GnRH)和促黄体生成素(LH)浓度激增,进而导致排卵。孕酮可阻断雌二醇诱导的GnRH/LH激增,但其涉及的机制尚不清楚。我们研究了孕酮对绵羊下丘脑/视前区(POA)内细胞的雌二醇诱导激活的影响,以确定:(i)孕酮在哪些区域发挥作用来阻断GnRH/LH激增,以及(ii)孕酮是直接还是间接阻止雌二醇反应性细胞的激活。通过测量表达Fos(一种即刻早期基因)的细胞数量来评估细胞激活情况。在LH激增诱导过程的激活阶段,在无孕酮(通常刺激LH激增)的情况下暴露于升高的雌二醇浓度,并未导致下丘脑Fos表达出现任何区域特异性变化(实验1)。相同处理在激增开始时显著增加了POA、外侧隔(LS)和弓状核内的细胞激活(实验2)。在激增诱导过程的激活阶段同时暴露于升高的雌二醇和孕酮浓度(通常阻断LH激增),与阳性对照(仅雌二醇增加)相比,腹内侧下丘脑和下丘脑前区的细胞激活显著减少,与阴性对照(雌二醇无增加)相比,激活阶段弓状核的细胞激活显著减少(实验1)。在激增开始时(实验2),激活期暴露于孕酮可阻止阳性对照的POA、LS和弓状核中出现的雌二醇诱导的细胞激活增加。这些结果表明,雌二醇和孕酮对绵羊大脑中产生排卵前GnRH/LH激增的区域内的细胞激活具有不同的区域和时间特异性影响。此外,在激活阶段暴露于孕酮的动物在激增开始时POA、LS和弓状核内缺乏细胞激活,这与孕酮可通过直接抑制这些区域中雌二醇诱导的细胞激活来阻断排卵前激增的假设一致。