Drouva S V, Laplante E, Kordon C
Neuroendocrinology. 1983 Nov;37(5):336-41. doi: 10.1159/000123572.
The phasic luteinizing hormone (LH) release observed in ovariectomized (OVX), estrogen-implanted rats was further amplified and advanced when progesterone (P) was given 4 h prior to the gonadotropin surge. In contrast, an inhibitory effect of P on the daily LH surge was observed when P was administered 16-36 h prior to LH peak. In order to determine whether this biphasic action of P is primarily exerted on the release of luteinizing hormone releasing hormone (LHRH), on the pituitary response to LHRH, or on both, mediobasal hypothalamic slices or pituitary fragments of adult OVX rats or of OVX rats pretreated with estrogen alone or in combination with P were tested in a perifusion system. Mediobasal hypothalamic slices were perifused in buffered (pH 7.2) oxygenated Locke's medium containing bacitracin (2 X 10(-5) M). In the absence of estrogen pretreatment, high (56 mM) concentrations of K+ were barely effective in releasing LHRH. Subcutaneous implantation of 17 beta-estradiol for 5 days markedly increased the amplitude of the LHRH secretory response to K+ depolarization. Additional administration of P (25 mg/rat s.c.) 4 h before sacrifice further amplified the K+-induced LHRH release. In contrast, the K+-evoked LHRH secretion was significantly inhibited when P was given 16 or 36 h before. Estradiol thus appears to facilitate the LHRH secretory response to depolarizing stimuli, whereas P either enhances or blocks the induced LHRH release depending upon its time of administration. At the pituitary level, the sensitivity of LHRH-induced LH release was also increased after estrogen pretreatment.(ABSTRACT TRUNCATED AT 250 WORDS)
在去卵巢(OVX)且植入雌激素的大鼠中观察到的促黄体生成素(LH)阶段性释放,在促性腺激素高峰前4小时给予孕酮(P)时会进一步增强并提前出现。相反,当在LH峰值前16 - 36小时给予P时,观察到P对每日LH高峰有抑制作用。为了确定P的这种双相作用主要是作用于促黄体生成素释放激素(LHRH)的释放、垂体对LHRH的反应,还是两者都有作用,在灌注系统中对成年OVX大鼠或仅用雌激素或雌激素与P联合预处理的OVX大鼠的下丘脑中间基底部切片或垂体片段进行了测试。下丘脑中间基底部切片在含有杆菌肽(2×10⁻⁵ M)的缓冲(pH 7.2)充氧洛克氏培养基中进行灌注。在没有雌激素预处理的情况下,高浓度(56 mM)的K⁺对释放LHRH几乎没有效果。皮下植入17β - 雌二醇5天显著增加了LHRH对K⁺去极化分泌反应的幅度。在处死前4小时额外给予P(25 mg/大鼠皮下注射)进一步增强了K⁺诱导的LHRH释放。相反,当在16或36小时前给予P时,K⁺诱发的LHRH分泌显著受到抑制。因此,雌二醇似乎促进了LHRH对去极化刺激的分泌反应,而P根据其给药时间要么增强要么阻断诱导的LHRH释放。在垂体水平,雌激素预处理后LHRH诱导的LH释放的敏感性也增加了。(摘要截短至250字)