Physiology of the Prolactin Releasing Peptides

催乳素释放肽的生理学

• 批准号: 7395023
• 负责人: Willis K. Samson
• 金额: $ 30.6万
• 依托单位: SAINT LOUIS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2001
• 资助国家: 美国
• 起止时间: 2001-06-01 至 2011-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7395023
• 关键词: Address; Adenylate Cyclase; Affect; Agreement; American; American Heart Association; Amides; Animals; Anterior Pituitary Gland; Antihypertensive Agents; Antisense Oligonucleotides; Argipressin; Attention; Autonomic nervous system; Baroreflex; Behavioral; Blood Pressure; Blood Pressure Monitors; Blood Volume; Brain; Brain Stem; CCL4 gene; Cardiovascular Physiology; Cardiovascular system; Catalytic RNA; Cell Count; Cell Line; Cells; Complement; Complex; Conscious; Corticosterone; Corticotropin; Corticotropin-Releasing Hormone; Cultured Cells; Data; Depressed mood; Desire for food; Development; Dopamine; Dose; Eating; Effectiveness; Embryo; Endocrine; Endocrinology; Experimental Designs; Failure; Food; Frequencies; Funding; Genetic Polymorphism; Goals; Grant; HPSE gene; Heart Rate; Hormonal; Hormones; Human; Hypothalamic structure; Immune Sera; In Vitro; Individual; Injection of therapeutic agent; Intake; Intervention; Journals; Knock-out; Lateral; Life; Manuscripts; Mediating; Mediation; Medicine; Messenger RNA; Metabolic; Metabolic syndrome; Methodology; Methods; Modality; Molecular; Molecular Medicine; Names; Neuraxis; Neuroendocrinology; Neurons; Neuropeptides; Neurosciences; Neurosecretory Systems; Neurotransmitters; Nucleus solitarius; Obesity; Oligonucleotides; Outcome; Oxytocin; PC12 Cells; Peptide Receptor; Peptides; Pharmacologic Actions; Pharmacology; Phospholipase C; Physiological; Physiology; Pituitary Gland; Play; Polymerase Chain Reaction; Population; Preparation; Pressoreceptors; Process; Production; Progress Reports; Prolactin; Prosencephalon; Protein Kinase C; Publishing; Publishing Peer Reviews; Purpose; RNA Interference; Rattus; Regulation; Reporting; Research Design; Reverse Transcriptase Polymerase Chain Reaction; Role; Side; Signal Transduction; Site; Sleep; Slice; Small Interfering RNA; Somatotropin; Stress; Structure; Structure of dorsomedial hypothalamic nucleus; Structure of nucleus infundibularis hypothalami; Sympathetic Nervous System; Syndrome; System; Tetrodotoxin; Thirst; Thymidine; Vasoactive Intestinal Peptide; Visceral; Water; Water consumption; Withdrawal; Work; Yang; adrenomedullin; biological adaptation to stress; brain research; cell growth; citrate carrier; cost; dorsal motor nucleus; drinking water; feeding; frontier; glycemic control; hindbrain; hypocretin; hypothalamic-pituitary-adrenal axis; in vivo; in vivo Model; insight; magnocellular; male; neuropeptide B; new technology; novel; orexin A; paraventricular nucleus; parvocellular; programs; prolactin-releasing peptide; receptor; research study; response; restraint stress; solute; stress management; tool

DESCRIPTION (provided by applicant): This is a rerevised, competitive renewal application (HL66023) that continues our examination of the physiologic relevance of recently described neuropeptides which we have demonstrated to act at least pharmacologically to stimulate stress hormone secretion (prolactin, PRL, and adrenocorticotropin, ACTH) by a brain site of action. Additionally, these peptides stimulate stress-related behavioral responses (activity) and at least one acts in brain to stimulate sympathetic activity resulting in increased blood pressure. These peptides (prolactin releasing peptide, PrRP; neuropeptide W, NPW; and neuropeptide B, NPB) are produced in separate populations of neurons in brain, many of which innervate the hypothalamic paraventricular nucleus (PVN), arcuate nucleus (ARC) and ventromedial and dorsomedial hypothalamic nuclei (VMH/DMH). All three peptides are contained in neurons that innervate autonomic centers in hypothalamus and brain stem. It is our goal to understand the roles these peptides play in the hypothalamic and extrahypothalamic responses to stress. We address multiple specific aims all related to the founding hypothesis that one or more of these peptides is essential for the endocrine and/or cardiovascular response to stress, under certain paradigms of stress. Our approach will be to demonstrate direct effects of these peptides on identified fore- and hindbrain neurons [e.g. in PVN, ARC, VMH/DMH, nucleus tractus solitarius (NTS), rostral lateral medulla (RVLM), and dorsal motor nucleus of the Vagus] using electrophysiologic, pharmacologic and single cell RT- PCR approaches. We will then attempt compromise of peptide production and examine hormone secretion in response to physical stress and the cardiovascular response to hypertensive and hypotensive challenge (i.e. baroreflex sensitivity). Understanding the normal mechanisms controlling the response to stress will reveal potential strategies for the management of stress in the human population and the cardiovascular and metabolic consequences of that stress. These studies may also provide insight into the central mechanisms contributing to development of the metabolic syndrome (Syndrome X), which is characterized by obesity, poor glycemic control, altered metabolic and autonomic function and a propensity for adverse cardiovascular outcomes. Additionally, these studies will provide further insight into the coordinated hormonal and autonomic responses to stress.

描述（由申请人提供）：这是一份重新修订的竞争性延续申请（HL 66023），继续我们对最近描述的神经肽的生理相关性进行检查，我们已证明这些神经肽至少可通过大脑作用部位刺激应激激素分泌（催乳素、PRL和促肾上腺皮质激素、ACTH）。此外，这些肽刺激与压力相关的行为反应（活动），并且至少一种在大脑中起作用以刺激交感神经活动，导致血压升高。这些肽（催乳素释放肽，PrRP;神经肽W，NPW;和神经肽B，NPB）在脑中的不同神经元群体中产生，其中许多神经元支配下丘脑室旁核（PVN）、弓状核（ARC）以及下丘脑腹内侧核和背内侧核（VMH/DMH）。所有这三种肽都包含在支配下丘脑和脑干自主神经中枢的神经元中。我们的目标是了解这些肽在下丘脑和下丘脑外应激反应中的作用。我们解决了多个具体的目标，所有相关的创始假设，这些肽中的一个或多个是必不可少的内分泌和/或心血管应激反应，在某些范式的压力。我们的方法是使用电生理学、药理学和单细胞RT-PCR方法证明这些肽对鉴定的前脑和后脑神经元[例如PVN、ARC、VMH/DMH、孤束核（NTS）、延髓头端外侧（RVLM）和迷走神经背侧运动核]的直接作用。然后，我们将尝试肽生产的妥协，并检查激素分泌对身体压力和心血管反应高血压和肥胖的挑战（即压力反射敏感性）。了解控制压力反应的正常机制将揭示人类压力管理的潜在策略以及压力对心血管和代谢的影响。这些研究还可以提供对导致代谢综合征（X综合征）发展的中枢机制的深入了解，其特征在于肥胖、血糖控制不良、代谢和自主神经功能改变以及不良心血管结局的倾向。此外，这些研究将进一步深入了解协调激素和自主神经对压力的反应。