Neural Regulation of Vasopressin Release

加压素释放的神经调节

• 批准号: 7098257
• 负责人: J Thomas Cunningham
• 金额: $ 29.2万
• 依托单位: UNIVERSITY OF TEXAS HLTH SCIENCE CENTER
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-09-15 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7098257
• 关键词: afferent nerve; blood volume; chorda tympani; cranial nerves; electrolyte balance; electrophysiology; enteric nervous system; facial nerve; histochemistry /cytochemistry; hormone regulation /control mechanism; hyponatremia; immunocytochemistry; laboratory rat; laryngeal nerves; neurons; neuroregulation; oxytocin; paraventricular nucleus; pathologic process; solitary tract nucleus; supraoptic nucleus; vagus nerve; vasopressins; water; water drinking behavior

DESCRIPTION (provided by applicant): The long-term goal of this research program is to determine the central pathways that regulate vasopressin release in order to understand how their dysfunction might contribute to pathophysiology. The regulation of vasopressin release may be of particular importance in understanding dilutional hyponatremia, a common hydromineral imbalance that increases the morbidity and mortality of patients with congestive heart failure. Normally, vasopressin release is transiently inhibited by water intake, and the failure of water intake to suppress circulating vasopressin could contribute to dilutional hyponatremia. The central nervous system mechanisms that mediate the inhibition of vasopressin by water intake are not known. Purpose: Previous studies indicate that afferents from the oropharyngeal cavity and the gastrointestinal system inhibit vasopressin release associated with water intake. The goal of this proposal is to define the role of oropharyngeal factors in the neural network that influences the release of vasopressin and oxytocin following water intake. Specific Aims: 1. To determine the contribution of gustatory and oropharyngeal afferents in the inhibition of vasopressin release by water intake. Hypothesis: The inhibition of vasopressin release by water intake involves oropharyngeal afferents from the IXth and Xth cranial nerves but not gustatory afferents of the Vllth cranial nerve. 2. Experiments will evaluate the contribution of the nucleus of the solitary tract (NTS) in the inhibition of vasopressin neurons in the rat supraoptic nucleus (SON) by water intake. Hypothesis: The inhibitory effects of water intake on SON neurons are mediated through NTS neurons that project to the parabrachial nucleus. 3. Test the role of the parabrachial nucleus (PBN) in the inhibition of vasopressin release by water intake. Hypothesis: The PBN is required for water intake to inhibit vasopressin release. 4. Test the role of the perinuclear zone (PNZ) of the SON in the inhibition of vasopressin neurons associated with water intake. Hypothesis: The PBN acts on the SON through the PNZ to inhibit vasopressin release following water intake. Methods: The studies will employ in vivo single unit electrophysiological recording with juxtacellular labeling, c-Fos immunocytochemistry in combination with retrograde track tracing and in situ hybridization histochemistry, and lesion studies with measurements of plasma vasopressin and oxytocin to test these hypotheses. Benefits: The results will provide new information regarding the control of vasopressin secretion and how these systems contribute to pathophysiology.

描述（由申请人提供）：本研究计划的长期目标是确定调节加压素释放的中枢通路，以了解其功能障碍如何导致病理生理学。加压素释放的调节对于了解稀释性低钠血症可能特别重要，稀释性低钠血症是一种常见的水矿物质失衡，会增加充血性心力衰竭患者的发病率和死亡率。正常情况下，加压素释放被水摄入短暂抑制，水摄入抑制循环加压素的失败可能导致稀释性低钠血症。介导水摄入抑制加压素的中枢神经系统机制尚不清楚。目的：先前的研究表明，来自口咽腔和胃肠道系统的传入抑制与水摄入相关的加压素释放。这项建议的目的是确定口咽因素在神经网络中的作用，影响水摄入后加压素和催产素的释放。具体目标：1。确定味觉和口咽传入在饮水抑制加压素释放中的作用。假设：水摄入对加压素释放的抑制涉及来自第IX和第X脑神经的口咽传入，但不涉及第VII脑神经的味觉传入。2.本实验旨在研究饮水对大鼠视上核（SON）内加压素神经元的抑制作用，并探讨孤束核（NTS）在其中的作用。假设：饮水对SON神经元的抑制作用是通过投射到臂旁核的NTS神经元介导的。3.测试臂旁核（PBN）在水摄入抑制加压素释放中的作用。假设：PBN是水摄入所必需的，以抑制加压素释放。4.测试SON核周区（PNZ）在抑制与水摄入相关的加压素神经元中的作用。假设：PBN通过PNZ作用于SON以抑制水摄入后的加压素释放。研究方法：这些研究将采用在体单单位电生理记录与神经细胞标记，c-Fos免疫细胞化学结合逆行追踪和原位杂交组织化学，和病变研究与测量血浆加压素和催产素，以测试这些假设。益处：该结果将提供关于加压素分泌控制以及这些系统如何促进病理生理学的新信息。