Larsen P J, Jukes K E, Chowdrey H S, Lightman S L, Jessop D S
Department of Anatomy, University of Copenhagen, Denmark.
Endocrinology. 1994 Apr;134(4):1635-9. doi: 10.1210/endo.134.4.8137725.
Neuropeptide-Y (NPY) is colocalized with vasopressin and oxytocin in magnocellular neurons of the hypothalamo-neurohypophysial system, and a very high density of NPY-binding sites is present within the neurohypophysis. To investigate the possibility that NPY exerts a modulatory role on the release of neurohypophysial hormones, we have studied the actions of NPY on potassium-evoked release of vasopressin and oxytocin from the rat neurointermediate lobe in vitro. NPY dose-dependently potentiated vasopressin release evoked by high extracellular potassium (56 mM), with a maximal enhancement of 223% (10(-7) M NPY). A similar effect was obtained with the Y2-selective agonist NPY-(13-36). In contrast, no effect on the potassium-evoked release of oxytocin was observed at this concentration. In the absence of Ca2+ in the incubation medium, NPY did not potentiate vasopressin secretion, indicating that the effect of NPY on potassium-evoked secretion of neurohypophysial vasopressin is critically dependent on extracellular calcium ions. The number of neurohypophysial NPY-binding sites is drastically down-regulated in animals subjected to chronic osmotic stimulation. In the present study, it was observed that the potentiating effect of NPY on vasopressin secretion was completely abolished in neurointermediate lobes recovered from animals that had been drinking 2% NaCl for 12 days, reflecting the concomitant down-regulation of neurohypophysial NPY-binding sites observed during this state. Finally, it was confirmed that stimulation by high K+ significantly evoked the release of endogenous NPY from neurointermediate lobes of the pituitary gland. The present results provide evidence that NPY selectively and potently enhances evoked vasopressin secretion. Considering the coexistence of the two neuropeptides in magnocellular hypothalamo-neurohypophysial neurons, this action is likely to be part of an autostimulatory feedforward loop. NPY may be an important component in the mechanisms associated with the control of body fluid homeostasis.
神经肽Y(NPY)与血管加压素和催产素在下丘脑-神经垂体系统的大细胞神经元中共同定位,并且神经垂体中存在非常高密度的NPY结合位点。为了研究NPY对神经垂体激素释放发挥调节作用的可能性,我们在体外研究了NPY对大鼠神经中间叶钾离子诱发的血管加压素和催产素释放的作用。NPY剂量依赖性地增强了高细胞外钾(56 mM)诱发的血管加压素释放,最大增强幅度为223%(10⁻⁷ M NPY)。Y2选择性激动剂NPY-(13 - 36)也得到了类似的效果。相比之下,在此浓度下未观察到对钾离子诱发的催产素释放有影响。在孵育培养基中不存在Ca²⁺的情况下,NPY不能增强血管加压素分泌,这表明NPY对神经垂体血管加压素钾离子诱发分泌的作用严重依赖于细胞外钙离子。在经受慢性渗透刺激的动物中,神经垂体NPY结合位点的数量急剧下调。在本研究中,观察到从饮用2% NaCl 12天的动物中回收的神经中间叶中,NPY对血管加压素分泌的增强作用完全消失,这反映了在此状态下观察到的神经垂体NPY结合位点的伴随下调。最后,证实高K⁺刺激显著诱发了垂体神经中间叶内源性NPY的释放。目前的结果提供了证据表明NPY选择性且有力地增强诱发的血管加压素分泌。考虑到这两种神经肽在下丘脑-神经垂体大细胞神经元中共存,这种作用可能是自刺激前馈回路的一部分。NPY可能是与体液稳态控制相关机制中的一个重要组成部分。