Mechanisms of action of angiotensin-II on C1 neurons.

血管紧张素-II 对 C1 神经元的作用机制。

• 批准号: 7674341
• 负责人: Seth D DePuy
• 金额: $ 5.01万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-01 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7674341
• 关键词: Address; Adrenergic Agents; Anesthesia procedures; Angiotensin II; Angiotensins; Blood Pressure; Brain; Brain Stem; Cardiovascular Diseases; Cardiovascular system; Catecholamines; Cells; Complement component C1s; Development; Disease; Foundations; Gene Targeting; Goals; Heart failure; Hyperactive behavior; Hypertension; In Vitro; Ion Channel; Label; Maintenance; Molecular; Mus; Neurons; Pathology; Pattern; Peptidyl-Dipeptidase A; Play; Population; Reflex action; Renin-Angiotensin System; Research; Reverse Transcriptase Polymerase Chain Reaction; Role; Slice; Subfamily lentivirinae; Up-Regulation; Vasomotor; adrenergic; base; in vivo; lentiviral-mediated; novel therapeutics; overexpression; public health relevance; receptor

DESCRIPTION (provided by applicant): The renin-angiotensin system (RAS) is present within the cardiovascular regulatory centers of the brainstem and is an important contributing factor to both hypertension and heart failure. RAS hyperactivity is thought to underlie much of the inappropriate sympathoexcitatory drive that is common to these diseases, though the mechanism is still unclear. The presympathetic neurons of the rostral ventrolateral medulla (RVLM), particularly the C1-adrenergic cell group, play an important role in the dynamic control of sympathetic vasomotor tone and are probable targets of this hyperactive RAS. Activity of the RVLM neurons is modulated by many factors including angidtensin-ll (Angll) which is generally stimulatory, though the molecular basis of this modulation is also not defined. Under pathological conditions, upregulation of the RAS, including AT1 receptors and angiotensin converting enzyme (ACE), produces a tonic activation of presympathetic neurons that can be abrogated by receptor antagonists or targeted gene disruption. Although studies have attempted to address the role of Angll receptors in regulating brainstem neurons and in promoting hypertension, the extent to which the Angll receptors expressed by the C1 neurons contribute to hypertension remains to be determined. Identifying the important ionic conductances that are modulated by Angll in C1 neurons (via in vitro recording) and determining the contribution of Angll receptors on these cells to promote the hypertensive state (via lentiviral-mediated, C1-selective overexpression of AT1) are the primary goals of this proposal. Results from these studies could serve as a foundation for the development of novel therapeutic strategies to treat these pathologies. PUBLIC HEALTH RELEVANCE: Hypertension (high blood pressure) is one of the most prevalent cardiovascular disorders, afflicting approximately 33.6% of the population. The research proposed herein will serve to advance our understanding of the specific mechanisms involved in the development and maintenance of this disease.

描述(申请人提供)：肾素-血管紧张素系统(RAS)存在于脑干的心血管调节中心，是高血压和心力衰竭的重要因素。RAS过度活跃被认为是这些疾病常见的不适当的交感兴奋驱动的基础，尽管机制尚不清楚。延髓头端腹外侧区(RVLM)的交感前神经元，尤其是C_1-肾上腺素能细胞群，在交感血管舒张性张力的动态调控中起着重要作用，可能是这种过度活跃的RAS的靶点。RVLM神经元的活动受许多因素的调节，包括血管紧张素-11(Ang11)，它通常是刺激性的，尽管这种调节的分子基础也不确定。在病理条件下，RAS，包括AT1受体和血管紧张素转换酶(ACE)的上调，导致交感前神经元的紧张性激活，这种激活可以被受体拮抗剂或靶向基因破坏所消除。尽管已有研究试图解决Ang11受体在调节脑干神经元和促进高血压中的作用，但由C1神经元表达的Ang11受体在多大程度上促进高血压的作用仍有待确定。本研究的主要目标是确定在C1神经元中受Ang11调节的重要离子电导(通过体外记录)，并确定这些细胞上的Ang11受体在促进高血压状态中的作用(通过慢病毒介导的、选择性地表达AT1)。这些研究的结果可以作为开发治疗这些病理的新治疗策略的基础。公共卫生相关性：高血压(高血压)是最常见的心血管疾病之一，大约33.6%的人口受到影响。本文提出的研究将有助于促进我们对该病发生和维持的具体机制的理解。