Regulation of Neuronal Excitability by Extracellular Calcium
Regulation of Neuronal Excitability by Extracellular Calcium
批准号:
8410035
负责人:
Dejian Ren
金额:
$33.78万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-02-01 至 2016-01-31
关键词:
AffinityAmino AcidsBiochemicalBrainBrain regionCalciumCalcium-Sensing ReceptorsCalmodulinCationsCellsChargeComplexCouplingDataDropsElectrophysiology (science)EpilepsyG Protein-Coupled Receptor GenesG-Protein-Coupled ReceptorsGTP-Binding ProteinsGeneticGoalsHealthHeartHippocampus (Brain)Hypocalcemia resultImageInhibitory Concentration 50Knock-outKnockout MiceMediatingMembraneMolecularMusMutant Strains MiceNervous system structureNeuronsParalysedPhosphatidylinositol 4,5-DiphosphatePhysiologicalProteinsRegulationRelative (related person)Ringer&aposs solutionRoleSecond Messenger SystemsSeizuresSignal PathwaySignal TransductionSurfaceSynaptic CleftTestingVentral Tegmental Areadensityexcitatory neuronextracellularin vivoneuronal excitabilitynovelprotein activationreceptorscreeningsecond messengervoltage
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The major goal of this proposal is to build on our several recent unexpected findings to understand how extracellular calcium regulates the basal excitability of neurons. Under pathophysiological conditions such as hypocalcemia and epilepsy, concentration of extracellular calcium can drop significantly in the brain. Extracellular calcium concentration can also change under physiological conditions in brain regions with high neuronal density and in microdomains such as the synaptic cleft. A decrease in extracellular calcium concentration usually excites neurons. The molecular mechanisms underlying the control by extracellular calcium are poorly understood, in contrast with the extensively investigated intracellular roles of calcium as a second messenger. We propose that a major mechanism by which extracellular calcium regulates excitability is through the NALCN cation channel we discovered. Using biochemical, electrophysiology and mouse genetics approaches, we will 1) determine the relative contribution of NALCN to the neuronal excitation by extracellular calcium in several brain regions; 2) define the structural requirements of the protein in the calcium sensitivity; and 3) uncover the signals that regulate the channel complex. Results from these studies will help us understand how body calcium regulates neuronal excitability at the molecular level under physiological and pathophysiological conditions such as paralysis, seizure and epilepsy.
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Regulation of Neuronal Excitability by Extracellular Calcium
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Cyclic Nucleotide-Activated Calcium Channels in Sperm
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Sodium Leak Channels and Regulation by Neurotransmitters
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Sodium Leak Channels and Regulation by Neurotransmitters
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Sodium Leak Channels and Regulation by Neurotransmitters
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资助金额:$32.85万
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Sodium Leak Channels and Regulation by Neurotransmitters
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资助金额:$35.0万
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Sodium Leak Channels and Regulation by Neurotransmitters
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Sodium Leak Channels and Regulation by Neurotransmitters
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资助金额:$35.0万
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财政年份:2008
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负责人:Dejian Ren
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依托单位:
Sodium Leak Channels and Regulation by Neurotransmitters
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项目类别:
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资助金额:$4.0万
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依托单位:
海外基金