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DEVELOPMENT&MODULATION OF CALCIUM CURRENTS IN NEOCORTEX

DEVELOPMENT&MODULATION OF CALCIUM CURRENTS IN NEOCORTEX
发展
批准号:
6639471
负责人:
Robert C Foehring
金额:
$17.75万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-01-01 至 2006-03-31

项目摘要

项目成果

Robert C Foehring的其他基金

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中文摘要
翻译
描述:(申请人摘要)
英文摘要
DESCRIPTION: (Applicant's Abstract) Neocortical pyramidal neurons are a model system for study of the mechanisms and significance of transduction of synaptic inputs into spike trains. Several aspects of this transduction process are Ca2+-dependent, including regulation of the interspike interval (ISI), spike frequency adaptation (SFA), spike timing and afterhyperpolarizations (AHPs). Pyramidal cells express at least five different high voltage-activated Ca2+ channels. We hypothesize that Ca2+ entry has different consequences for these cells, depending upon which calcium channel subtypes are involved. An example of such partitioning of function is generation of AHPs: N-, P-, and Q-type channels couple to the sAHP and P-type to the mAHP. Two critical negative feedback systems controlling Ca2+ entry are Ca2+-dependent inactivation of Ca2+ channels and activation of Ca2+-dependent K+ channels. Both processes are potential regulators of pyramidal cell firing behavior. We will use whole cell electrical recordings and fura-2 Ca2+ imaging techniques on mature pyramidal cells in both acutely dissociated and brain slice preparations to test hypotheses about the roles of Ca2+-dependent inactivation and the relationships between action potentials, [Ca2+]i, and AHP currents (due to Ca2+-dependent K+ channels). Aim 1 addresses the importance of Ca2+-dependent inactivation of Ca2+ channel subtypes and which channel subtypes are involved. Aim 2 characterizes the relationships between firing frequency, IAHP, and [Ca2+]i in mature pyramidal cells. These data are important for understanding how pyramidal cells integrate synaptic inputs, and how this process is influenced by transmitters and ontogeny. (In neocortical pyramidal neurons, both Ca2+ and Ca2+-dep K+ channels are developmentally regulated and are targets for several neuromodulators). Neuronal activity and its modulation regulate cortical function and the use-dependent plasticity of cortical connections. These studies will contribute to understanding essential cortical functions such as attention, learning, and memory as well as basic mechanisms of diseases such as epilepsy, anxiety and depression.
期刊论文(12)
专著(0)
科研奖励(0)
会议论文
Serotonergic modulation of supragranular neurons in rat sensorimotor cortex.
大鼠感觉运动皮层颗粒上神经元的血清素调节。
DOI: 10.1523/jneurosci.22-18-08238.2002
发表时间: 2002
期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子: --
作者: [Foehring,RC, vanBrederode,JFM, Kinney,GA, Spain,WJ]
通讯作者: Spain,WJ
DOI: 10.1097/00001756-199906230-00029
发表时间: 1999-06
期刊: Neuroreport
影响因子: 1.7
作者: [J. C. Pineda;E. Galarraga;R. Foehring]
通讯作者: J. C. Pineda;E. Galarraga;R. Foehring
alpha2-Adrenergic receptor-mediated modulation of calcium current in neocortical pyramidal neurons.
α2-肾上腺素受体介导的新皮质锥体神经元钙电流调节。
DOI: 10.1016/j.brainres.2004.04.025
发表时间: 2004
期刊: Brain research.
影响因子: --
作者: [Timmons,SD, Geisert,E, Stewart,AE, Lorenzon,NM, Foehring,RC]
通讯作者: Foehring,RC
Morphological and electrophysiological properties of atypically oriented layer 2 pyramidal cells of the juvenile rat neocortex.
幼年大鼠新皮质非典型定向第 2 层锥体细胞的形态学和电生理学特性。
DOI: 10.1016/s0306-4522(00)00430-9
发表时间: 2000
期刊: Neuroscience
影响因子: 3.3
作者: [vanBrederode,JF, Foehring,RC, Spain,WJ]
通讯作者: Spain,WJ
共 7 条
    Role of inhibition in shaping neocortical activity: normal vs fmr1 knockout mouse
    Slowly Inactivating K+ Channels in Pyramidal Neurons
    Slowly Inactivating K+ Channels in Pyramidal Neurons
    Dynamics of Kv channel function in identified populations of pyramidal neurons in neocortex
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