Sensory receptors of the vagus nerve
迷走神经的感觉感受器
基本信息
- 批准号:9151840
- 负责人:
- 金额:$ 118.65万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2016
- 资助国家:美国
- 起止时间:2016-09-30 至 2021-07-31
- 项目状态:已结题
- 来源:
- 关键词:AchievementAfferent NeuronsAsthmaAutonomic nervous system disordersBiologyBlood PressureBrainBreathingCardiovascular systemCellsClinicalColitisCoughingCuesDiabetes MellitusEpilepsyFeeding behaviorsFundingFunding MechanismsGangliaGoalsHeart RateImageImmune systemIrritantsLungMechanoreceptorsMediatingMental DepressionMetabolismMolecularNauseaNervous System controlNeuronsObesityOrganPhysiologicalPhysiologyPressoreceptorsPublicationsRNA InterferenceRespirationRespiratory SystemRiskSensorySensory ReceptorsSmell PerceptionStimulusStomachStretchingSurveysSystemTaste PerceptionTouch sensationToxinVagus nerve structureVisionWorkaortic archbody systemgastrointestinal systemgene functionin vivoinsightloss of functionneurophysiologyneurotransmissionnovelreceptorresponsesensory systemtherapy design
项目摘要
Project Summary
The discoveries of primary sensory receptors that mediate our external senses of smell, touch, taste, and
vision were landmark achievements. In contrast, internal sensory systems of the vagus nerve are vastly
understudied at a molecular level, with primary sensory receptors unknown in any organ system. The
vagus nerve is a major conduit between brain and body that controls feeding behavior, respiration, blood
pressure, metabolism, heart rate, nausea, and cough. Mechanosensory and chemosensory transduction
mechanisms in the vagus nerve present tremendously important problems in sensory biology. Sensory
receptors that detect meal-induced stomach distension, blood pressure at the aortic arch, lung expansion
during breathing, irritants that cause cough, or chemotherapeutics that induce nausea are unknown.
Understanding how the vagus nerve signals at a molecular level is relevant for a wide range of clinical
conditions, including obesity, diabetes, colitis, asthma, nausea, depression, and epilepsy.
The goals of this project are to identify primary sensory receptors of the vagus nerve that survey internal
organ state. Initial efforts will focus on finding stomach and lung mechanoreceptors as well as aortic
baroreceptors, and work could be extended to identify irritant and toxin receptors that evoke cough and
nausea. Vagal mechanoreceptors will be identified using a novel in vivo ganglion imaging approach that
permits analysis of single neuron responses to internal organ stimuli. In vivo ganglion imaging is
compatible with mosaic loss-of-function approaches like RNAi for analysis of gene function.
Deconstructing the sensory biology of vagal afferents will reveal basic insights into how autonomic
physiology is controlled by the nervous system, and may provide new opportunities for therapy design.
This proposal builds on years of foundational work, and is not supportable by traditional funding
mechanisms due to the large project scope, the risk associated with receptor-identification studies, and
my limited publication record in this new field. So far, our early work in this system has characterized
sensory neuron types in different physiological systems (Cell, 2015). Funding would enable new
molecular-level efforts to identify primary sensory receptor proteins that detect internal sensory cues.
项目摘要
初级感觉感受器的发现,介导我们的嗅觉,触觉,味觉,
愿景是里程碑式的成就。相比之下,迷走神经的内部感觉系统
在分子水平上研究不足,初级感觉受体在任何器官系统中都是未知的。的
迷走神经是大脑和身体之间的主要管道,控制进食行为、呼吸、血液
血压、新陈代谢、心率、恶心和咳嗽。机械感觉和化学感觉转导
迷走神经中的机制在感觉生物学中提出了极其重要的问题。感官
感受器检测由进食引起的胃扩张、主动脉弓处的血压、肺扩张
在呼吸过程中,引起咳嗽的刺激物或引起恶心的化疗药物是未知的。
了解迷走神经如何在分子水平上发出信号,
这些疾病包括肥胖、糖尿病、结肠炎、哮喘、恶心、抑郁和癫痫。
这个项目的目标是确定初级感觉受体的迷走神经,调查内部
器官状态最初的努力将集中在寻找胃和肺机械感受器以及主动脉
压力感受器,工作可以扩展到确定刺激和毒素受体,引起咳嗽,
恶心迷走神经机械感受器将使用一种新的体内神经节成像方法进行鉴定,
允许分析单个神经元对内部器官刺激的反应。体内神经节成像是
与用于分析基因功能的镶嵌功能丧失方法如RNAi相容。
解构迷走神经传入的感觉生物学将揭示自主神经如何
生理学是由神经系统控制的,并且可以为治疗设计提供新的机会。
这项提案建立在多年的基础工作之上,传统的资金无法支持
由于项目范围大,与受体识别研究相关的风险,
我在这个新领域的有限出版记录。到目前为止,我们在这一系统中的早期工作的特点是,
不同生理系统中的感觉神经元类型(Cell,2015)。资金将使新
分子水平的努力,以确定初级感觉受体蛋白,检测内部的感觉线索。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
STEPHEN Daniel LIBERLES其他文献
STEPHEN Daniel LIBERLES的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('STEPHEN Daniel LIBERLES', 18)}}的其他基金
Area postrema neurons that mediate nausea-associated behaviors
介导恶心相关行为的后区神经元
- 批准号:
10440136 - 财政年份:2022
- 资助金额:
$ 118.65万 - 项目类别:
Area Postrema Neurons that Mediate Nausea-Associated Behaviors
介导恶心相关行为的后区神经元
- 批准号:
10573276 - 财政年份:2022
- 资助金额:
$ 118.65万 - 项目类别:
Leveraging the Rich Genetic Diversity of Vagal Motor Neurons to Decode Brain-to-Gut Communication
利用迷走神经运动神经元丰富的遗传多样性来解码脑肠通讯
- 批准号:
10443804 - 财政年份:2019
- 资助金额:
$ 118.65万 - 项目类别:
Leveraging the Rich Genetic Diversity of Vagal Motor Neurons to Decode Brain-to-Gut Communication
利用迷走神经运动神经元丰富的遗传多样性来解码脑肠通讯
- 批准号:
10206129 - 财政年份:2019
- 资助金额:
$ 118.65万 - 项目类别:
Leveraging the Rich Genetic Diversity of Vagal Motor Neurons to Decode Brain-to-Gut Communication
利用迷走神经运动神经元丰富的遗传多样性来解码脑肠通讯
- 批准号:
10653096 - 财政年份:2019
- 资助金额:
$ 118.65万 - 项目类别:
Leveraging the Rich Genetic Diversity of Vagal Motor Neurons to Decode Brain-to-Gut Communication
利用迷走神经运动神经元丰富的遗传多样性来解码脑肠通讯
- 批准号:
10019337 - 财政年份:2019
- 资助金额:
$ 118.65万 - 项目类别:
Charting vagal circuits containing glucagon-like peptide 1 receptor
绘制含有胰高血糖素样肽 1 受体的迷走神经回路
- 批准号:
9222742 - 财政年份:2016
- 资助金额:
$ 118.65万 - 项目类别:
Sensory biology of respiratory control neurons in the vagus nerve
迷走神经呼吸控制神经元的感觉生物学
- 批准号:
9077705 - 财政年份:2016
- 资助金额:
$ 118.65万 - 项目类别:
Sensory biology of respiratory control neurons in the vagus nerve
迷走神经呼吸控制神经元的感觉生物学
- 批准号:
9273635 - 财政年份:2016
- 资助金额:
$ 118.65万 - 项目类别:
Charting vagal circuits containing glucagon-like peptide 1 receptor
绘制含有胰高血糖素样肽 1 受体的迷走神经回路
- 批准号:
9095676 - 财政年份:2016
- 资助金额:
$ 118.65万 - 项目类别:
相似海外基金
How Spinal Afferent Neurons Control Appetite and Thirst
脊髓传入神经元如何控制食欲和口渴
- 批准号:
DP220100070 - 财政年份:2023
- 资助金额:
$ 118.65万 - 项目类别:
Discovery Projects
The mechanisms of the signal transduction from brown adipocytes to afferent neurons and its significance.
棕色脂肪细胞向传入神经元的信号转导机制及其意义。
- 批准号:
23K05594 - 财政年份:2023
- 资助金额:
$ 118.65万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
- 批准号:
10477437 - 财政年份:2021
- 资助金额:
$ 118.65万 - 项目类别:
GPR35 on Vagal Afferent Neurons as a Peripheral Drug Target for Treating Diet-Induced Obesity
迷走神经传入神经元上的 GPR35 作为治疗饮食引起的肥胖的外周药物靶点
- 批准号:
10315571 - 财政年份:2021
- 资助金额:
$ 118.65万 - 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
- 批准号:
10680037 - 财政年份:2021
- 资助金额:
$ 118.65万 - 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
- 批准号:
10654779 - 财政年份:2021
- 资助金额:
$ 118.65万 - 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
- 批准号:
10275133 - 财政年份:2021
- 资助金额:
$ 118.65万 - 项目类别:
GPR35 on Vagal Afferent Neurons as a Peripheral Drug Target for Treating Diet-Induced Obesity
迷走神经传入神经元上的 GPR35 作为治疗饮食引起的肥胖的外周药物靶点
- 批准号:
10470747 - 财政年份:2021
- 资助金额:
$ 118.65万 - 项目类别:
Roles of mechanosensory ion channels in myenteric intrinsic primary afferent neurons
机械感觉离子通道在肌间固有初级传入神经元中的作用
- 批准号:
RGPIN-2014-05517 - 财政年份:2018
- 资助金额:
$ 118.65万 - 项目类别:
Discovery Grants Program - Individual
Roles of mechanosensory ion channels in myenteric intrinsic primary afferent neurons
机械感觉离子通道在肌间固有初级传入神经元中的作用
- 批准号:
RGPIN-2014-05517 - 财政年份:2017
- 资助金额:
$ 118.65万 - 项目类别:
Discovery Grants Program - Individual














{{item.name}}会员




