Sagrillo C A, Selmanoff M
Center for Studies in Reproduction, Department of Physiology, University of Maryland, School of Medicine, 655 West Baltimore Street, Baltimore, MD 21201-1559, USA.
Brain Res Mol Brain Res. 1998 Oct 30;61(1-2):62-8. doi: 10.1016/s0169-328x(98)00198-3.
Prolactin (PRL) exerts a short-loop negative feedback effect on hypothalamic neurons which control its secretion from the anterior pituitary gland. The purpose of this study was to identify the location of hypothalamic neurons which respond to acute PRL exposure. Increasing evidence indicates that excitation of neurons often results in the rapid transcription of immediate early genes (IEGs). In the present study, quantitative in situ hybridization histochemistry (ISHH) was used to visualize the induction of mRNAs for four different IEGs: zif/268 (NGF1-A), nur/77 (NGF1-B), c-fos and c-jun. Three groups of male rats were compared: unmanipulated controls, rats injected s.c. with 2.4 mg ovine PRL (oPRL) suspended in polyvinylpyrrolidone (PVP), and PVP-injected controls. Animals were decapitated 0, 0.5, 1, 2, 3 or 4 h following injection. In all rats, the four probes labeled cells within the cortex, particularly the cingulate and piriform cortices, the hippocampus and the striatum. In the arcuate nucleus, there was a modest increase in the average number of cells/animal which expressed zif/268 mRNA following the injection of PVP and oPRL at all times studied. The average area of grains/cell representing zif/268 message also increased following the injection stimulus. The number of neurons expressing nur/77 mRNA was greater in PRL-treated rats compared with PVP-treated controls 0.5 and 1 h following injection. Nur/77-labeled neurons were co-extensive with the tuberoinfundibular dopaminergic (TIDA) neurons. The data suggest that cells located within the arcuate nucleus are involved in mediating PRL autofeedback on the brain.
催乳素(PRL)对控制其从前脑垂体分泌的下丘脑神经元发挥短环负反馈作用。本研究的目的是确定对急性PRL暴露有反应的下丘脑神经元的位置。越来越多的证据表明,神经元的兴奋通常会导致即刻早期基因(IEGs)的快速转录。在本研究中,定量原位杂交组织化学(ISHH)用于可视化四种不同IEGs的mRNA诱导情况:zif/268(NGF1-A)、nur/77(NGF1-B)、c-fos和c-jun。比较了三组雄性大鼠:未处理的对照组、皮下注射悬浮于聚乙烯吡咯烷酮(PVP)中的2.4mg绵羊PRL(oPRL)的大鼠以及注射PVP的对照组。在注射后0、0.5、1、2、3或4小时将动物断头。在所有大鼠中,这四种探针标记了皮质内的细胞,特别是扣带回和梨状皮质、海马体和纹状体。在弓状核中,在所有研究时间点,注射PVP和oPRL后,表达zif/268 mRNA的细胞/动物平均数量有适度增加。代表zif/268信息的颗粒/细胞平均面积在注射刺激后也增加。与注射PVP的对照组相比,PRL处理的大鼠在注射后0.5和1小时表达nur/77 mRNA的神经元数量更多。Nur/77标记的神经元与结节漏斗多巴胺能(TIDA)神经元共同分布。数据表明,位于弓状核内的细胞参与介导PRL对大脑的自身反馈。