Properties of Axons and Synaptic Communication in the Neocortex
Properties of Axons and Synaptic Communication in the Neocortex
批准号:
7456275
负责人:
David McCormick
金额:
$38.22万
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 2012-01-31
关键词:
Action PotentialsAffectAnimalsAxonBrainBrain regionBuffersCalciumCellsCerebral cortexCharacteristicsCodeCommunicationDendritesDiseaseDisruptionDoseEpilepsyEvoked PotentialsExcitatory Postsynaptic PotentialsFailureFerretsGenerationsImageIn VitroIndividualInformation and Communication TheoryInterneuronsInvestigationIon ChannelKnock-outLocationMSMB geneMediatingMembrane PotentialsMultiple SclerosisMusNeocortexNeuronsOutputParentsPatternPhysiologic pulsePotassium ChannelPrefrontal CortexPresynaptic TerminalsProbabilityPropertyPublic HealthPulse takingPyramidal CellsRateRestSliceSourceSynapsesSynaptic PotentialsSynaptic TransmissionTimeToxinTrainingTravelVariantWhole-Cell Recordingsanalogdendrotoxindigitalin vivoinsightinterestnervous system disorderneuronal cell bodyneurotransmitter releasepatch clamppostsynapticpresynapticresearch studyresponsetransmission processtwo-photonvoltagevoltage clamp
中文摘要
描述(由申请人提供):传统上,大脑皮层中的神经元之间的通信,以及实际上在大脑的大部分内的通信,被认为主要或仅通过脉冲或数字代码中的动作电位的速率和模式来介导。然而,最近,我们已经表明,由动作电位诱发的突触电位的平均幅度依赖于突触前神经元的膜电位,这些膜电位的变化沿轴突传播很长的距离。这意味着附近皮层神经元之间的信息通信可能使用组合脉冲和分级或模拟和数字代码。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可以影响神经元在附近细胞中诱导的突触电位的幅度的机制。我们将从体外保存的前额叶皮层切片中突触连接的神经元对进行全细胞记录。此外,我们将研究可能参与的变化,突触前钙浓度通过双光子成像的钙离子水平在突触前扣,而他们的父母索马被移动到不同的膜电位。我们的研究也将探讨皮质内轴突的电生理特性,特别是那些可能参与检测索马膜电位变化的特性。我们特别感兴趣的是在皮层内轴突的电压依赖性K+电流的属性,以及这些如何可能控制轴突的兴奋性。为了详细检查这些,我们将在电压钳步骤的应用期间从皮层神经元的索马和轴突进行同时的全细胞膜片钳记录,并检查轴突对不同类型的K+通道特异性的毒素的应用的响应。在敲除特定K+通道的小鼠中,从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。通过这种突触和轴突电生理学的研究相结合,我们将实现一个更详细和综合的了解如何在大脑皮层内的信息沟通。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)的正常功能对大脑的正常功能至关重要,特别是大脑皮层。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中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.
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