Properties of Axons and Synaptic Communication in the Neocortex
Properties of Axons and Synaptic Communication in the Neocortex
批准号:
8018559
负责人:
David McCormick
金额:
$35.48万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-02-15 至 2012-04-30
关键词:
Action PotentialsAnimalsAxonBrainCalciumCellsCerebral cortexCodeCommunicationDataDiseaseEpilepsyFinancial compensationHealthImageIn VitroInvestigationIon ChannelKnock-outMediatingMembrane PotentialsMultiple SclerosisMusN-Methyl-D-Aspartate ReceptorsNeocortexNeuronsNifedipineOutputParentsPatternPhysiologic pulsePotassium ChannelPresynaptic TerminalsPropertyRestRouteRyanodineSliceSourceSpecificitySynapsesSynaptic PotentialsSynaptic TransmissionTestingThapsigarginTimeToxinTravelWhole-Cell Recordingsanalogchannel blockersd-APVdigitalinterestnervous system disorderneuronal cell bodypatch clamppresynapticreceptorresearch studyresponsetooltwo-photonvoltagevoltage clamp
中文摘要
描述(由申请人提供):传统上,大脑皮层中神经元之间的交流,实际上,在大脑的大部分,被认为主要或完全通过脉冲或数字代码中的动作电位的速率和模式来调节。然而,最近,我们已经表明,动作电位引起的突触电位的平均振幅取决于突触前神经元的膜电位,这些膜电位的变化沿着轴突传播很长一段距离。这意味着附近皮层神经元之间的信息交流可能使用脉冲和渐变或模拟和数字代码的组合。在这里,我们将研究这种可能的模拟代码的机制。具体来说,我们将研究皮层神经元的膜电位如何影响神经元在附近细胞中诱导的突触电位振幅的机制。我们将在体外保存的前额皮质切片中对突触连接的神经元进行全细胞记录。此外,我们将检查可能参与突触前钙浓度的变化,通过双光子成像的Ca2+水平在突触前钮扣,当他们的亲本体细胞移动到不同的膜电位。我们的研究还将检查皮质内轴突的电生理特性,特别是那些可能涉及检测体细胞膜电位变化的特性。我们对皮质轴突内电压依赖性K+电流的特性以及这些电流如何控制轴突兴奋性特别感兴趣。为了详细研究这些,我们将在施加电压钳步骤期间同时对皮质神经元的体细胞和轴突进行全细胞膜片钳记录,并检查轴突对不同类型K+通道特异性毒素的反应。通过对特定K+通道被敲除的小鼠的皮质内轴突进行全细胞记录,我们将能够检查特定离子通道和亚基在这些效应中的参与情况。通过突触和轴突电生理研究的结合,我们将对大脑皮层内的信息交流如何运作有更详细和更全面的了解。这些信息将使我们能够更好地管理轴突和突触通讯障碍,包括多发性硬化症和癫痫。公共卫生相关性:突触传递和轴突(神经元的输出)的正常功能对大脑,特别是大脑皮层的正常功能至关重要。许多神经系统疾病是由突触和轴突功能的破坏引起的。我们的研究将探讨大脑皮层突触和轴突功能的重要基本特性。
英文摘要
DESCRIPTION (provided by applicant): Traditionally, communication between neurons in the cerebral cortex, and, indeed, within much of the brain, is believed to be mediated largely or solely through the rate and pattern of action potentials in a pulse or digital code. Recently, however, we have shown that the average amplitude of synaptic potentials evoked by action potentials is dependent upon the membrane potential of the presynaptic neuron and that these membrane potential changes travel long distances down the axon. This means that information communication between nearby cortical neurons may use a combined pulse and graded or analog and digital code. Here we will examine the mechanisms of this possible analog code. Specifically, we will examine the mechanisms by which the membrane potential of cortical neurons can influence the amplitude of synaptic potentials that the neuron induces in nearby cells. We will perform whole cell recordings from synaptically connected pairs of neurons in prefrontal cortical slices maintained in vitro. In addition, we will examine the possible involvement of changes in presynaptic Calcium concentrations through two-photon imaging of Ca2+ levels in presynaptic boutons while their parent soma is moved to different membrane potentials. Our investigations will also examine the electrophysiological properties of intracortical axons, particularly those properties that may be involved in detecting changes in membrane potential at the soma. We are particularly interested in the properties of voltage-dependent K+ currents within intracortical axons and how these may control axonal excitability. To examine these in detail, we will perform simultaneous whole cell patch clamp recordings from the soma and axon of cortical neurons during the application of voltage clamp steps and examine the respond of the axons to the application of toxins that are specific for different types of K+ channel. Be performing whole cell recordings from intracortical axons in mice in which particular K+ channels have been knocked out, we will be able to examine the involvement of specific ionic channels and subunits in these effects. Through this combination of synaptic and axonal electrophysiological investigations, we will achieve a more detailed and integrated understanding of how information communication operates within the cerebral cortex. This information will allow us to better manage disorders of axonal and synaptic communication including multiple sclerosis and epilepsy. PUBLIC HEALTH RELEVANCE: The proper function of synaptic transmission and axons, the output of neurons, is critical to the proper functioning of the brain, particularly the cerebral cortex. Numerous neurological disorders result from disruption of synaptic and axonal function. Our study will examine important basic properties of synaptic and axonal function in the cerebral cortex.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1523/jneurosci.1613-08.2008
发表时间:
2008-07-16
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
[Yu Y, Shu Y, McCormick DA]
通讯作者:
McCormick DA
Somatic membrane potential and Kv1 channels control spike repolarization in cortical axon collaterals and presynaptic boutons.
体膜电位和KV1通道控制皮质轴突侧支和突触前胸子中的尖峰复极化。
DOI:
10.1523/jneurosci.2752-11.2011
发表时间:
2011-10-26
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
[Foust AJ, Yu Y, Popovic M, Zecevic D, McCormick DA]
通讯作者:
McCormick DA
DOI:
10.1523/jneurosci.0552-10.2010
发表时间:
2010-05-19
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
[Foust A, Popovic M, Zecevic D, McCormick DA]
通讯作者:
McCormick DA
Brain States and Flexible Behavior
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批准号:10700739
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项目类别:
-
资助金额:$74.87万
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财政年份:2020
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负责人:David McCormick
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依托单位:
LFA-9 (mPGES-1/5-LOX Inhibitor): Preclinical Studies to Support a Clinical Trial,
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批准号:10399397
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项目类别:
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资助金额:$84.42万
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财政年份:2018
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负责人:David McCormick
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依托单位:
LFA-9 (mPGES-1/5-LOX Inhibitor): Preclinical Studies to Support a Clinical Trial,
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批准号:10794912
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项目类别:
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资助金额:$41.87万
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财政年份:2018
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负责人:David McCormick
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依托单位:
IGF::OT::IGF NExT Preclinical Toxicology & Pharmacology of Drugs Developed for Cancer Patients, TO#3, Exploratory Studies of CCR4 CART Cells
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批准号:10361380
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资助金额:$23.86万
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财政年份:2017
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依托单位:
Mechanisms of Rapid Modulation of Auditory Responsiveness
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批准号:10055961
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资助金额:$31.34万
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财政年份:2016
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负责人:David McCormick
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依托单位:
Cortical Dynamics and Neural/Behavioral Performance
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批准号:10544429
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项目类别:
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资助金额:$7.38万
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财政年份:2016
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负责人:David McCormick
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依托单位:
Cortical Dynamics and Neural/Behavioral Performance
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批准号:10530597
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项目类别:
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资助金额:$81.13万
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财政年份:2016
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负责人:David McCormick
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依托单位:
Cortical Dynamics and Neural/Behavioral Performance
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批准号:10058278
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项目类别:
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资助金额:$73.75万
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财政年份:2016
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负责人:David McCormick
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依托单位:
Cortical Dynamics and Neural/Behavioral Performance
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批准号:10304870
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项目类别:
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资助金额:$73.75万
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财政年份:2016
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负责人:David McCormick
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依托单位:
CALCIUM SIGNALING AND PREFRONTAL DEFICITS IN SCHIZOPHRENIA
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批准号:7958212
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项目类别:
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资助金额:$4.39万
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财政年份:2009
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负责人:David McCormick
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依托单位:
Properties of Axons and Synaptic Communication in the Neocortex
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批准号:7760193
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项目类别:
-
资助金额:$35.84万
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财政年份:2008
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负责人:David McCormick
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依托单位:
Properties of Axons and Synaptic Communication in the Neocortex
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批准号:7456275
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项目类别:
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资助金额:$38.22万
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财政年份:2008
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负责人:David McCormick
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依托单位:
Properties of Axons and Synaptic Communication in the Neocortex
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批准号:7816554
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项目类别:
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资助金额:$52.99万
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财政年份:2008
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负责人:David McCormick
-
依托单位:
Properties of Axons and Synaptic Communication in the Neocortex
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批准号:7564071
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项目类别:
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资助金额:$36.2万
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财政年份:2008
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负责人:David McCormick
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依托单位:
CALCIUM SIGNALING AND PREFRONTAL DEFICITS IN SCHIZOPHRENIA
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批准号:7715811
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项目类别:
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资助金额:$2.85万
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财政年份:2008
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负责人:David McCormick
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依托单位:
CALCIUM SIGNALING AND PREFRONTAL DEFICITS IN SCHIZOPHRENIA
-
批准号:7562680
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项目类别:
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资助金额:$3.16万
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财政年份:2007
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负责人:David McCormick
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依托单位:
Calcium Signaling & Prefrontal Deficits in Schizophrenia
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批准号:7321074
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项目类别:
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资助金额:$161.88万
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财政年份:2003
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负责人:David McCormick
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依托单位:
Calcium Signaling & Prefrontal Deficits in Schizophrenia
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批准号:7162228
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项目类别:
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资助金额:$167.2万
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财政年份:2003
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负责人:David McCormick
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依托单位:
Calcium Signaling & Prefrontal Deficits in Schizophrenia
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批准号:7148689
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项目类别:
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资助金额:$223.53万
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财政年份:2003
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负责人:David McCormick
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依托单位:
DEVELOPMENT OF NETWORK ACTIVITY IN THALAMOCORTICAL CIRCUITS
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批准号:6354126
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项目类别:
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资助金额:$10.17万
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财政年份:2000
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负责人:David McCormick
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依托单位:
海外基金