Neurotransmitter Metabolism in Intermittent Hypoxia

间歇性缺氧中的神经递质代谢

• 批准号: 7464291
• 负责人: Ganesh K Kumar
• 金额: $ 38.38万
• 依托单位: UNIVERSITY OF CHICAGO
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-04-01 至 2012-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7464291
• 关键词: Abbreviations; Acute; Adrenal Glands; Adrenal Medulla; Adrenalectomy; Adult; Affect; Animals; Apnea; Attenuated; Biological; Blood; Blood Pressure; Calcium; Calcium Channel; Calcium Signaling; Cardiovascular Abnormalities; Cardiovascular system; Catecholamines; Chronic; Continuous Positive Airway Pressure; Coupled; Data; Detection; Development; Disruption; Elevation; Enzyme Immunoassay; Epinephrine; Evaluation; Figs - dietary; GTP-Binding Proteins; Generations; Genetic; Glycine; Goals; High Pressure Liquid Chromatography; Hormones; Human; Hypertension; Hypoxia; Intervention; Knockout Mice; Literature; Mediating; Messenger RNA; Methods; Mixed Function Oxygenases; Monitor; Morbidity - disease rate; Mus; Nerve; Neuropeptide Y Receptor; Norepinephrine; Obstructive Sleep Apnea; Patients; Peptides; Peripheral; Plasma; Play; Population; Process; Proteolytic Processing; Public Health; Rattus; Reactive Oxygen Species; Reagent; Recruitment Activity; Recurrence; Reporting; Research Design; Risk; Role; Signal Transduction; Sleep Apnea Syndromes; Slice; Stimulus; Sympathetic Nervous System; Testing; United States; Wild Type Mouse; amidation; awake; base; design; experience; in vivo; inhibitor/antagonist; insight; mortality; neuropeptide Y; neurotransmitter metabolism; novel therapeutics; peptidylglycine alpha-amidating monooxygenase; prevent; receptor; research study; respiratory; response; therapeutic target; voltage

DESCRIPTION (provided by applicant): Humans, experiencing chronic intermittent hypoxia (CIH), are prone to develop hypertension. Previous studies showed that rats and mice exposed to CIH have increased blood pressure, elevated circulating catecholamines (CA) and increased levels of vasoactive substances including norepinephrine and neuropeptide Y (NPY) in the adrenal medulla. To begin to define the mechanism(s) by which CIH evokes cardiovascular changes, we propose to test the following interlinked hypotheses: i) CIH facilitates the synthesis and stimulus-evoked release of NPY; ii) Exogenously released NPY, in turn, via activation of NPY receptor subtypes and the downstream G-protein mediated signaling cascade contributes to CIH-induced increases in CA release, and iii) CIH-evoked functional interaction between NPY and CA in the sympathetic nervous system contributes to cardiovascular changes elicited by CIH. These hypotheses will be tested in the adrenal medulla of rats exposed to CIH. In Aim 1, the effects of CIH on the synthesis of bioactive NPY both at the mRNA (preproNPY) and at the peptide levels and the potential contribution of peptidylglycine a-amidating monooxygenase (PAM) in CIH-induced alterations in NPY levels will be assessed. In Aim 2, the effects of CIH on stimulus-evoked NPY release and the role of cytosolic calcium in eliciting this response will be determined. Studies in Aim 3 will examine the critical role(s) of NPY Y receptors (Y1 and Y2) and G-protein mediated cell signaling in CIH-induced facilitation of CA release by hypoxia. To delineate the potential contribution of NPY receptor subtypes, the effects of NPY receptor subtype specific antagonists and targeted deletion of NPY receptor subtypes on CIH-evoked changes in CA release will be assessed. Studies in Aim 4 are designed to assess the direct and/or indirect contributions of NPY and its receptor subtypes and PAM to CIH-evoked cardiovascular changes in unanesthetized, awake animals. It is anticipated that the proposed studies will provide new mechanistic insights into CIH-evoked functional alterations in the peripheral sympathetic nervous system and aid in the identification of novel therapeutic targets for effective intervention of cardiovascular abnormalities associated with recurrent apneas. PUBLIC HEALTH RELEVANCE. Sleep-disordered breathing with recurrent apneas is a major cause of morbidity and mortality in the United States population, affecting an estimated 18 million people. Patients with chronic intermittent hypoxia (CIH) caused by sleep apnea have a greatly increased risk for the development of systemic hypertension. The mechanism(s) by which CIH associated with recurrent apneas are initiated leading to cardio-respiratory morbidity, however, are not fully understood. The proposal aims to elucidate the role of functional interactions between two potent vasoactive substances such as neuropeptide Y and catecholamines in the peripheral sympathetic nervous system in CIH-evoked elevation in blood pressure. These studies are expected to provide new therapeutic targets for alleviating the cardiovascular morbidity associated with recurrent apneas.

描述（由申请人提供）：经历慢性间歇性缺氧（CIH）的人类容易患上高血压。先前的研究表明，暴露于CIH的大鼠和小鼠血压升高，循环中的儿茶酚胺（CA）升高，肾上腺髓质中的血管活性物质（包括去甲肾上腺素和神经肽Y（NPY））水平升高。为了开始定义CIH引起心血管变化的机制，我们提出了以下相互关联的假设：i）CIH促进NPY的合成和刺激诱发的释放; ii）外源性释放的NPY，反过来，通过激活NPY受体亚型和下游G蛋白介导的信号级联，有助于CIH诱导的CA释放增加，和iii）CIH诱发的交感神经系统中NPY和CA之间的功能相互作用有助于CIH诱发的心血管变化。这些假设将在暴露于CIH的大鼠肾上腺髓质中进行检验。在目的1中，将评估CIH在mRNA（preproNPY）和肽水平上对生物活性NPY的合成的影响，以及肽基甘氨酸α-酰胺化单加氧酶（PAM）在CIH诱导的NPY水平改变中的潜在贡献。在目标2中，CIH对刺激诱发的NPY释放的影响以及胞浆钙在引起这种反应中的作用将被确定。目的3中的研究将检查NPY Y受体（Y1和Y2）和G蛋白介导的细胞信号传导在CIH诱导的缺氧促进CA释放中的关键作用。为了描述NPY受体亚型的潜在贡献，将评估NPY受体亚型特异性拮抗剂和NPY受体亚型的靶向缺失对CIH诱发的CA释放变化的影响。目的4中的研究旨在评估NPY及其受体亚型和PAM对未麻醉清醒动物中CIH诱发的心血管变化的直接和/或间接贡献。预计这些研究将为CIH诱发的外周交感神经系统功能改变提供新的机制见解，并有助于确定有效干预与复发性呼吸暂停相关的心血管异常的新治疗靶点。公共卫生相关性。睡眠呼吸障碍伴复发性呼吸暂停是美国人口发病率和死亡率的主要原因，估计影响1800万人。由睡眠呼吸暂停引起的慢性间歇性缺氧（CIH）患者发生全身性高血压的风险大大增加。然而，与复发性呼吸暂停相关的CIH引发导致心肺疾病的机制尚未完全了解。该提案旨在阐明CIH诱发的血压升高中两种有效的血管活性物质（如神经肽Y和儿茶酚胺）在外周交感神经系统中的功能相互作用的作用。这些研究有望为缓解与复发性呼吸暂停相关的心血管发病率提供新的治疗靶点。