He J R, Molnar J, Barraclough C A
Department of Physiology, School of Medicine, University of Maryland, Baltimore 21201-1559.
Brain Res Mol Brain Res. 1993 Oct;20(1-2):71-8. doi: 10.1016/0169-328x(93)90111-2.
In these studies we examined the temporal effects of intracerebroventricular (i.c.v.) infusions of norepinephrine (NE) on plasma LH and on LHRH mRNA levels in the organum vasculosum of the lamina terminalis (OVLT) and in neurons located in the rostral (r), middle (m) and caudal (c) preoptic areas (POA) of ovariectomized, estrogen-treated rats. Thereafter, we compared these responses to those which occur in androgen-sterilized rats (ASR). NE infusions not only increased plasma LH concentrations but within 1 h after NE, LHRH mRNA levels also were increased significantly in the OVLT and rPOA but not in the mPOA or cPOA. By 4 h, these message levels still were elevated in the OVLT and rPOA and they now also were significantly higher than control values in the mPOA and cPOA. While NE also increased LH secretion in ASR, the plasma LH concentrations obtained were markedly blunted compared to control values. Moreover, NE infusions did not alter single cell levels of LHRH mRNA in any region of the rostral hypothalamus. Previously, we have reported that morphine (s.c.) markedly amplifies NE-induced LH release and questioned whether these responses are accompanied by concomitant augmented increases in LHRH mRNA levels. Morphine alone did not affect basal LHRH mRNA or plasma LH levels. However, when rats were pretreated with morphine (-15 min) and NE was infused i.c.v. at 0 time, significant amplification of LH release occurred but, unexpectedly, morphine completely blocked NE-induced increases in LHRH mRNA levels in all of the neurons we examined. Morphine also amplified LH release in ASR but these responses were significantly less than those obtained in control rats.(ABSTRACT TRUNCATED AT 250 WORDS)
在这些研究中,我们检测了向去卵巢并经雌激素处理的大鼠脑室内注射去甲肾上腺素(NE)对血浆促黄体生成素(LH)以及终板血管器(OVLT)和位于视前区头端(r)、中间(m)及尾端(c)的神经元中促性腺激素释放激素(LHRH)mRNA水平的时间效应。之后,我们将这些反应与雄激素绝育大鼠(ASR)的反应进行了比较。注射NE不仅使血浆LH浓度升高,而且在注射NE后1小时内,OVLT和视前区头端(rPOA)中的LHRH mRNA水平也显著升高,但视前区中间(mPOA)和尾端(cPOA)则未升高。到4小时时,OVLT和rPOA中的这些信息水平仍然升高,并且此时它们也显著高于mPOA和cPOA中的对照值。虽然NE也增加了ASR中的LH分泌,但与对照值相比,所测得的血浆LH浓度明显降低。此外,注射NE并未改变视前区头端下丘脑任何区域中LHRH mRNA的单细胞水平。此前,我们曾报道吗啡(皮下注射)可显著增强NE诱导的LH释放,并质疑这些反应是否伴随着LHRH mRNA水平的相应增加。单独使用吗啡并不影响基础LHRH mRNA或血浆LH水平。然而,如果大鼠预先注射吗啡(-15分钟)并在0时刻脑室内注射NE,则会出现LH释放的显著增强,但出乎意料的是,吗啡完全阻断了我们所检测的所有神经元中NE诱导的LHRH mRNA水平的升高。吗啡也增强了ASR中的LH释放,但这些反应明显小于在对照大鼠中所获得的反应。(摘要截选至250字)