Housham S J, Terenzi M G, Ingram C D
Department of Anatomy, University of Bristol, U.K.
Neuroscience. 1997 Nov;81(2):479-88. doi: 10.1016/s0306-4522(97)00202-9.
Oxytocin acts within the limbic system (bed nuclei of the stria terminalis and ventrolateral septum) to induce maternal behaviour and to facilitate neuroendocrine activity at specific times during the peripartum period. Studies were undertaken to determine whether the timing of these effects arises from modulation of the oxytocin-induced excitation of limbic neurons. Extracellular activity of single units was recorded on urethane-anaesthetized rats and neurons were tested for responses to intracerebroventricular injection of 1.1 ng oxytocin. In the first part, animals were recorded on days 19 and 22 of pregnancy and on days 3 and 5 of lactation. No significant differences in the basal firing rates or in the proportion of oxytocin-responsive neurons were detected, but responses by neurons on day 22 of pregnancy occurred after a significant delay (10.7 +/- 2.0 min), resulting in a smaller overall response compared to the other groups. These differences in the pattern of response were not due to changes in density of oxytocin binding in the limbic areas studied, since autoradiographic detection of oxytocin binding sites using the iodinated antagonist [125I]d(CH2)5[Tyr(Me)2, Thr4, Orn3, Tyr-NH2(9)]-vasotocin showed no differences between the pregnant and postpartum animals. In the second part, parturient animals (day 22 of pregnancy) received intravenous injection of the long-acting opioid antagonist naltrexone, or unilateral knife-cut lesions to the stria terminalis, a source of inhibitory inputs (including enkephalinergic) to the bed nuclei of the stria terminalis and ventrolateral septum. Both treatments abolished the characteristic delay of oxytocin-induced excitation in non-treated animals on day 22 of pregnancy, and increased the overall excitatory response. Thus, during the peripartum period, a population of limbic neurons sensitive to oxytocin display a dynamically changing pattern of excitatory responses, apparently modulated by an endogenous opioid cone and independent of changes in oxytocin receptor expression. The attenuated neuronal response to central oxytocin seen on the day of parturition could account for the absence of a facilitatory effect of oxytocin on neuroendocrine activity at this time.
催产素作用于边缘系统(终纹床核和腹外侧隔区),以诱导母性行为,并在围产期的特定时间促进神经内分泌活动。开展了多项研究,以确定这些效应的时间安排是否源于催产素诱导的边缘神经元兴奋的调节。在乌拉坦麻醉的大鼠身上记录单个神经元的细胞外活动,并测试神经元对脑室内注射1.1纳克催产素的反应。在第一部分中,在妊娠第19天和第22天以及哺乳第3天和第5天对动物进行记录。未检测到基础放电率或催产素反应性神经元比例的显著差异,但妊娠第22天的神经元反应出现了显著延迟(10.7±2.0分钟),与其他组相比,总体反应较小。反应模式的这些差异并非由于所研究边缘区域中催产素结合密度的变化,因为使用碘化拮抗剂[125I]d(CH2)5[Tyr(Me)2, Thr4, Orn3, Tyr-NH2(9)]-血管加压素进行的催产素结合位点的放射自显影检测显示,妊娠动物和产后动物之间没有差异。在第二部分中,分娩动物(妊娠第22天)接受长效阿片类拮抗剂纳曲酮的静脉注射,或对终纹进行单侧刀切损伤,终纹是向终纹床核和腹外侧隔区提供抑制性输入(包括脑啡肽能输入)的来源。两种处理均消除了未处理动物在妊娠第22天催产素诱导兴奋的特征性延迟,并增加了总体兴奋反应。因此,在围产期,一群对催产素敏感的边缘神经元表现出动态变化的兴奋反应模式,显然受内源性阿片类物质的调节,且与催产素受体表达的变化无关。分娩当天观察到的神经元对中枢催产素的反应减弱,可能解释了此时催产素对神经内分泌活动缺乏促进作用的原因。