P450 Eicosannoids: Novel Nerve-Deerived Relaxing Factors in the Brain

P450 二十烷酸:大脑中新型神经源性放松因子

基本信息

  • 批准号:
    7450806
  • 负责人:
  • 金额:
    $ 4.1万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2007
  • 资助国家:
    美国
  • 起止时间:
    2007-06-01 至 2010-05-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Blood flow to the brain is tightly coupled to local metabolic demand through signaling mechanisms collectively termed neurovascular coupling (NVC). A number of endogenous regulators of NVC have been identified including astrocyte-derived P450 vasodilator eicosanoids referred to as epoxyeicosatrienoic acids (EETs). At the regional level, cerebral blood flow (CBF) is regulated in part by extrinsic perivascular vasodilator and vasoconstrictor nerves that innervate conduit arteries such as the middle cerebral (MCA) and basilar arteries (BAS). We provide herein preliminary data demonstrating the expression of EETs synthetic and metabolizing enzymes within parasympathetic vasodilator perivascular nerves. Based on these findings, we propose to test the hypothesis that EETs are novel parasympathetic nerve-derived relaxing factors involved in the neurogenic regulation of CBF. We will first utilize immunofluorescent double-labeling, Western blot, real-time quantitative RT-PCR (rtqRT-PCR) and anterograde nerve tracing to characterize the expression of EETs-synthetic enzyme cytochrome P450 2C11 epoxygenase and EETs-inactivating enzyme soluble epoxide hydrolase (sEH) within the cerebral vascular nerves and their ganglia of origin. We will then utilize an in vivo cranial window preparation to determine the functional role of EETs in the neurogenic vasodilator response of the MCA to parasympathetic ganglia stimulation. Lastly, we will employ compartmented co-culture model of parasympathetic neurons (PSN) and vascular smooth muscle cells (VSMC) to determine the mechanism of EETs release by parasympathetic neurons and their hyperpolarizing action upon VSMC. The proposed studies will explore a novel mechanism of CBF regulation, which will further our understanding of CBF regulation under physiological conditions, and may have important clinical implications relevant to neurovascular dysfunction in such disease states as vasospasm after subarachnoid hemorrhage, vascular dementia, migraine, stroke and traumatic brain injury.
描述(由申请人提供):通过统称为神经血管偶联(NVC)的信号传导机制,流向大脑的血流与局部代谢需求紧密偶联。已经鉴定了许多NVC的内源性调节剂,包括星形胶质细胞衍生的P450血管扩张剂类二十烷酸,称为环氧二十碳三烯酸(ECONOID)。在区域水平上,脑血流(CBF)部分地由支配管道动脉(诸如大脑中动脉(MCA)和基底动脉(BAS))的外源性血管周围血管扩张神经和血管收缩神经调节。我们在此提供的初步数据表明,在副交感神经血管扩张血管周围神经内的表达的肾上腺素合成和代谢酶。基于这些发现,我们建议测试的假设,即Escherichia coli是新的副交感神经源性的放松因子参与神经源性调节的CBF。我们将首先利用免疫荧光双标记、Western blot、实时定量RT-PCR(rtqRT-PCR)和顺行神经追踪来表征EETs合成酶细胞色素P450 2C 11环氧合酶和EETs失活酶可溶性环氧化物水解酶(sEH)在脑血管神经及其起源神经节中的表达。然后,我们将利用在体颅窗准备,以确定在MCA的神经源性血管扩张反应的副交感神经节刺激的功能性作用,肾上腺素。最后,我们将利用副交感神经元(PSN)和血管平滑肌细胞(VSMC)的分室共培养模型来研究副交感神经元释放E2的机制及其对VSMC的超极化作用。这些研究将探索一种新的脑血流调节机制,这将进一步加深我们对生理条件下脑血流调节的理解,并可能对蛛网膜下腔出血后血管痉挛、血管性痴呆、偏头痛、中风和创伤性脑损伤等疾病状态下的神经血管功能障碍具有重要的临床意义。

项目成果

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Jeffrey J Iliff其他文献

Jeffrey J Iliff的其他文献

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{{ truncateString('Jeffrey J Iliff', 18)}}的其他基金

Tai Chi Practice and Sleep-Active Glymphatic Function
太极拳练习和睡眠活跃类淋巴功能
  • 批准号:
    10583904
  • 财政年份:
    2023
  • 资助金额:
    $ 4.1万
  • 项目类别:
The role of post-traumatic sleep-wake disruption in the development of tau pathology following mild traumatic brain injury
创伤后睡眠觉醒中断在轻度创伤性脑损伤后 tau 病理学发展中的作用
  • 批准号:
    10588916
  • 财政年份:
    2023
  • 资助金额:
    $ 4.1万
  • 项目类别:
Role of Sleep Disruption after mTBI as a Driver of Chronic Post-traumatic Headache
mTBI 后睡眠中断是慢性创伤后头痛的驱动因素
  • 批准号:
    10736602
  • 财政年份:
    2023
  • 资助金额:
    $ 4.1万
  • 项目类别:
Research Education Component
研究教育部分
  • 批准号:
    10661555
  • 财政年份:
    2020
  • 资助金额:
    $ 4.1万
  • 项目类别:
Research Education Component
研究教育部分
  • 批准号:
    10171549
  • 财政年份:
    2020
  • 资助金额:
    $ 4.1万
  • 项目类别:
Research Education Component
研究教育部分
  • 批准号:
    9921711
  • 财政年份:
    2020
  • 资助金额:
    $ 4.1万
  • 项目类别:
Research Education Component
研究教育部分
  • 批准号:
    10433874
  • 财政年份:
    2020
  • 资助金额:
    $ 4.1万
  • 项目类别:
Defining the role of age-related glymphatic pathway impairment in amyloid beta plaque deposition
定义年龄相关的类淋巴通路损伤在淀粉样β斑块沉积中的作用
  • 批准号:
    10198706
  • 财政年份:
    2017
  • 资助金额:
    $ 4.1万
  • 项目类别:
Defining the role of age-related glymphatic pathway impairment in amyloid beta plaque deposition
定义年龄相关的类淋巴通路损伤在淀粉样β斑块沉积中的作用
  • 批准号:
    10003575
  • 财政年份:
    2017
  • 资助金额:
    $ 4.1万
  • 项目类别:
Defining the role of age-related glymphatic pathway impairment in amyloid beta plaque deposition
定义年龄相关的类淋巴通路损伤在淀粉样β斑块沉积中的作用
  • 批准号:
    9214181
  • 财政年份:
    2017
  • 资助金额:
    $ 4.1万
  • 项目类别:

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