Pau K Y, Gliessman P M, Hess D L, Ronnekleiv O K, Levine J E, Spies H G
Division of Reproductive Biology and Behavior, Oregon Regional Primate Research Center, Beaverton 97006.
Brain Res. 1990 May 28;517(1-2):229-35. doi: 10.1016/0006-8993(90)91031-b.
The pattern of hypothalamic gonadotropin-releasing hormone (GnRH) release was examined during estrogen (E)-induced suppression of plasma luteinizing hormone (LH) in ovariectomized (OVX) rhesus macaques. In Expt. 1, 4 OVX macaques were fitted with a jugular catheter and a push-pull cannula (PPC) directed into the median eminence (ME). Push-pull perfusion (PPP) was initiated 10 h before and continued for 10 h after subcutaneous estradiol benzoate (EB) injection (42 micrograms/kg b.wt.). In Expt. 2, 4 additional monkeys were subjected to local intrahypothalamic perfusion with estradiol-17 beta (E2, 3 microM) for the last 10 h of a 20-h PPP. In Expt. 2, OVX animals were challenged with 5 micrograms exogenous GnRH 3 h before and 8 h after EB injection to test for changes in altered LH release. Integrated 10-min ME perfusate and intermittent 10- or 60-min peripheral plasma samples were assayed for GnRH and LH by radioimmunoassay and bioassay, respectively. In addition, 2 other OVX macaques that received similar ME-PPC placement were sacrificed 2 days after the completion of a PPP for immunocytochemical labeling of GnRH neurons at the perfusion site. The results show that after EB, hypothalamic GnRH (MBH-GnRH) release remained unaltered while LH levels declined rapidly (Expt. 1). Similarly, intrahypothalamic perfusion of E2 failed to change the pattern of MBH-GnRH release in any of 4 monkeys (Expt. 2). Conversely, plasma LH release in response to exogenous GnRH was greatly reduced after EB (Expt. 3).(ABSTRACT TRUNCATED AT 250 WORDS)
在雌激素(E)诱导的去卵巢(OVX)恒河猴血浆促黄体生成素(LH)抑制过程中,研究了下丘脑促性腺激素释放激素(GnRH)的释放模式。在实验1中,4只去卵巢猕猴安装了颈静脉导管和指向正中隆起(ME)的推挽式套管(PPC)。在皮下注射苯甲酸雌二醇(EB,42微克/千克体重)前10小时开始推挽式灌注(PPP),并在注射后持续10小时。在实验2中,另外4只猴子在20小时PPP的最后10小时接受下丘脑内局部灌注17β-雌二醇(E2,3微摩尔)。在实验2中,去卵巢动物在EB注射前3小时和注射后8小时用5微克外源性GnRH进行刺激,以测试LH释放变化。分别通过放射免疫测定法和生物测定法对10分钟的ME灌流液和间歇性10或60分钟的外周血浆样本进行GnRH和LH测定。此外,在完成PPP后2天,处死另外2只接受类似ME-PPC放置的去卵巢猕猴,对灌注部位的GnRH神经元进行免疫细胞化学标记。结果显示,注射EB后,下丘脑GnRH(MBH-GnRH)释放未改变,而LH水平迅速下降(实验1)。同样,4只猴子中的任何一只在下丘脑内灌注E2后,MBH-GnRH释放模式均未改变(实验2)。相反,注射EB后,对外源性GnRH的血浆LH释放反应大大降低(实验3)。(摘要截断于250字)