DEVELOPMENT/MODULATION OF CALCIUM CURRENTS IN NEOCORTEX
DEVELOPMENT/MODULATION OF CALCIUM CURRENTS IN NEOCORTEX
批准号:
6091942
负责人:
Robert C Foehring
金额:
$22.96万
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 2004-03-31
关键词:
G protein adenylate cyclase biological signal transduction calcium channel calcium flux developmental neurobiology laboratory rat membrane potentials neural plasticity neuronal transport neuropharmacology neurophysiology norepinephrine phosphorylation potassium channel protein kinase A pyramidal cells serotonin receptor voltage /patch clamp voltage gated channel
中文摘要
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(0)
专著(0)
科研奖励(0)
会议论文
Role of inhibition in shaping neocortical activity: normal vs fmr1 knockout mouse
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批准号:7581035
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项目类别:
-
资助金额:$7.35万
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财政年份:2008
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负责人:Robert C Foehring
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依托单位:
Dynamics of Kv channel function in identified populations of pyramidal neurons in neocortex
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批准号:10335207
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项目类别:
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资助金额:$46.65万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly Inactivating K+ Channels in Pyramidal Neurons
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批准号:6844743
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项目类别:
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资助金额:$31.05万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly Inactivating K+ Channels in Pyramidal Neurons
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批准号:6703733
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项目类别:
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资助金额:$30.32万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly Inactivating K+ Channels in Neocortical Pyramidal Cells
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批准号:7620053
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项目类别:
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资助金额:$31.13万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly Inactivating K+ Channels in Pyramidal Neurons
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批准号:7020639
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项目类别:
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资助金额:$30.24万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly Inactivating K+ Channels in Neocortical Pyramidal Cells
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批准号:8096622
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项目类别:
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资助金额:$31.3万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Dynamics of Kv channel function in identified populations of pyramidal neurons in neocortex
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批准号:9514597
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项目类别:
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资助金额:$49.16万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly Inactivating K+ Channels in Neocortical Pyramidal Cells
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批准号:7525117
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项目类别:
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资助金额:$28.88万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly inactivating K+ channels in neocortical pyramidal cells
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批准号:8382988
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项目类别:
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资助金额:$36.72万
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财政年份:2003
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负责人:Robert C Foehring
-
依托单位:
Slowly inactivating K+ channels in neocortical pyramidal cells
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批准号:8681548
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项目类别:
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资助金额:$33.5万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly Inactivating K+ Channels in Pyramidal Neurons
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批准号:6609057
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项目类别:
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资助金额:$30.1万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
Slowly Inactivating K+ Channels in Neocortical Pyramidal Cells
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批准号:7860483
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项目类别:
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资助金额:$31.62万
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财政年份:2003
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负责人:Robert C Foehring
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依托单位:
DEVELOPMENT AND MODULATION OF CALCIUM CURRENTS IN CORTEX
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批准号:2272450
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项目类别:
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资助金额:$13.81万
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财政年份:1995
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负责人:Robert C Foehring
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依托单位:
DEVELOPMENT AND MODULATION OF CALCIUM CURRENTS IN CORTEX
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批准号:2272452
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项目类别:
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资助金额:$3.33万
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财政年份:1995
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负责人:Robert C Foehring
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依托单位:
DEVELOPMENT AND MODULATION OF CALCIUM CURRENTS IN CORTEX
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批准号:2272451
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项目类别:
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资助金额:$10.05万
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财政年份:1995
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负责人:Robert C Foehring
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依托单位:
DEVELOPMENT AND MODULATION OF CALCIUM CURRENTS IN CORTEX
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批准号:2635756
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项目类别:
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资助金额:$13.21万
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财政年份:1995
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负责人:Robert C Foehring
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依托单位:
DEVELOPMENT&MODULATION OF CALCIUM CURRENTS IN NEOCORTEX
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批准号:6639471
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项目类别:
-
资助金额:$17.75万
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财政年份:1995
-
负责人:Robert C Foehring
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依托单位:
DEVELOPMENT&MODULATION OF CALCIUM CURRENTS IN NEOCORTEX
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批准号:6393693
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项目类别:
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资助金额:$17.75万
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财政年份:1995
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负责人:Robert C Foehring
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依托单位:
DEVELOPMENT AND MODULATION OF CALCIUM CURRENTS IN CORTEX
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批准号:2037872
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项目类别:
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资助金额:$15.12万
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财政年份:1995
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负责人:Robert C Foehring
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依托单位:
海外基金