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催乳素对雌激素诱导的大鼠下丘脑 - 垂体顺序灌流中促黄体生成素分泌的抑制作用。

Suppressive effect of prolactin on oestrogen-induced secretion of LH by sequentially perifused rat hypothalamus-pituitary.

作者信息

Lee J W, Miyake A, Tasaka K, Otsuka S, Aono T, Kurachi K

出版信息

Acta Endocrinol (Copenh). 1985 Feb;108(2):151-5. doi: 10.1530/acta.0.1080151.

Abstract

The effect of prolactin (Prl) on oestrogen-induced gonadotrophin secretion was examined in vitro in a sequential double chamber perfusion system. As control groups, mediobasal hypothalamus (MBH)-pituitary pairs or pituitaries without the MBHs were perifused with Medium 199. As an experimental group, MBH-pituitary pairs were perifused with Medium 199 containing 1 micrograms/ml of rat Prl. These groups were stimulated with 10(-7) M oestradiol-17 beta (E2) for 30 min, and luteinizing hormone (LH) in the serial fractions of effluent was measured. In the control group of MBH-pituitary pairs perifused with medium without Prl, secretion of LH began to rise within 30 min after the beginning of stimulation, reached a peak 30 min after the end of stimulation and then remained at a plateau for the rest of the experimental period, whereas in the control group of pituitaries alone no significant response was observed. In the experimental group perifused with medium containing Prl, LH-secretion showed peaks 20 and 80 min after the end of E2-stimulation, respectively, and the first peak was significantly (P less than 0.01) less than the level in the control group. These data demonstrate that Prl at this concentration suppressed the rapid LH release induced by E2. Its site of action is suggested to be at the hypothalamic level, and its possible mechanism of action is discussed.

摘要

在体外,采用连续双室灌注系统研究了催乳素(Prl)对雌激素诱导的促性腺激素分泌的影响。作为对照组,将中基底下丘脑(MBH)-垂体对或不含MBH的垂体用199培养基进行灌注。作为实验组,将MBH-垂体对用含有1微克/毫升大鼠Prl的199培养基进行灌注。用10⁻⁷M雌二醇-17β(E2)刺激这些组30分钟,并测定流出液连续部分中的促黄体生成素(LH)。在灌注不含Prl的培养基的MBH-垂体对对照组中,刺激开始后30分钟内LH分泌开始上升,刺激结束后30分钟达到峰值,然后在实验期的剩余时间保持在平台期,而在仅垂体的对照组中未观察到明显反应。在灌注含Prl培养基的实验组中,LH分泌分别在E2刺激结束后20分钟和80分钟出现峰值,且第一个峰值显著低于对照组水平(P<0.01)。这些数据表明,该浓度的Prl抑制了E2诱导的LH快速释放。提示其作用部位在下丘脑水平,并对其可能的作用机制进行了讨论。

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