Micevych Paul, Sinchak Kevin, Mills Richard H, Tao Leslie, LaPolt Philip, Lu John K H
Department of Neurobiology, David Geffen School of Medicine at UCLA, Laboratory of Neuroendocrinology, Brain Research Institute, University of California, Los Angeles, Calif., USA.
Neuroendocrinology. 2003 Jul;78(1):29-35. doi: 10.1159/000071703.
As circulating estrogen levels rise on the afternoon of proestrus, they stimulate the hypothalamo-pituitary axis. This estrogen positive feedback is pivotal to stimulate the luteinizing hormone (LH) surge required for ovulation and luteinization of ovarian follicles. In addition to estrogen, pre-LH surge progesterone is critical for an LH surge as was demonstrated by blocking progesterone synthesis. In ovariectomized (OVX) rats treated with trilostane, a blocker of the enzyme 3beta-hydroxysteroid dehydrogenase (3beta-HSD) that catalyzes the conversion of pregnenolone to progesterone, estrogen did not induce an LH surge. Further, estrogen induced an LH surge in OVX and adrenalectomized (ADX) rats, indicating that the source of progesterone was neither the ovary nor adrenal gland. This estrogen-only LH surge was inhibited by pretreatment with trilostane, indicating that although the adrenal gland and ovary were not necessary for positive feedback, progesterone synthesis was critical for estrogen-induced positive feedback in an OVX/ADX rat. This suggested that the LH surge is dependent on the pre-LH surge synthesis of progesterone. Estrogen-induced progesterone receptors in the hypothalamus are vital for the LH surge, so a potential location for progesterone synthesis is the hypothalamus. OVX/ADX female rats were treated with 17beta-estradiol (50 microg) and progesterone levels were assayed by RIA. Progesterone levels were elevated in hypothalamic tissue following estrogen treatment. No increases in tissue progesterone levels were found in parietal cortex, cerebellum, medulla, pituitary or plasma. Additionally, male rats that do not have an estrogen positive feedback-induced LH surge were examined. Castrated/ADX male rats had no increase in hypothalamic progesterone levels after estrogen treatment. Together, these data strongly suggest that estrogen enhances neuroprogesterone synthesis in the hypothalamus that is involved in the positive feedback regulating the LH surge.
在动情前期下午,随着循环雌激素水平升高,它们刺激下丘脑 - 垂体轴。这种雌激素正反馈对于刺激排卵和卵巢卵泡黄素化所需的促黄体生成素(LH)峰至关重要。除了雌激素外,LH峰前的孕酮对于LH峰也很关键,这已通过阻断孕酮合成得到证实。在用曲洛司坦治疗的去卵巢(OVX)大鼠中,曲洛司坦是催化孕烯醇酮转化为孕酮的3β - 羟基类固醇脱氢酶(3β - HSD)的抑制剂,雌激素并未诱导LH峰。此外,雌激素在OVX和肾上腺切除(ADX)大鼠中诱导了LH峰,表明孕酮的来源既不是卵巢也不是肾上腺。这种仅由雌激素诱导的LH峰被曲洛司坦预处理所抑制,表明尽管肾上腺和卵巢对于正反馈不是必需的,但孕酮合成对于OVX/ADX大鼠中雌激素诱导的正反馈至关重要。这表明LH峰依赖于LH峰前孕酮的合成。雌激素诱导的下丘脑孕酮受体对于LH峰至关重要,因此孕酮合成的一个潜在部位是下丘脑。用17β - 雌二醇(50微克)处理OVX/ADX雌性大鼠,并通过放射免疫分析测定孕酮水平。雌激素处理后下丘脑组织中的孕酮水平升高。在顶叶皮质、小脑、延髓、垂体或血浆中未发现组织孕酮水平升高。此外,对没有雌激素正反馈诱导的LH峰的雄性大鼠进行了检查。去势/ADX雄性大鼠在雌激素处理后下丘脑孕酮水平没有增加。总之,这些数据强烈表明雌激素增强了下丘脑中参与调节LH峰正反馈的神经孕酮合成。