Cholinergic control of neural network function
Cholinergic control of neural network function
批准号:
8264401
负责人:
ADAM RORY MCQUISTON
金额:
$37.38万
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:
2011-05-13 至 2016-01-31
关键词:
AcetylcholineAddressAffectAgonistAlzheimer&aposs DiseaseAreaAxonBindingBiological Neural NetworksBrainCellsCholinergic AgonistsCholinergic FibersCholinergic ReceptorsComplexDendritesDiagonal Band of BrocaDiffuseDiffusionDyesElectric StimulationExtracellular SpaceFunctional disorderGoalsHippocampus (Brain)ImageIndividualInjection of therapeutic agentInterneuron functionInterneuronsKineticsLifeLightMeasuresMedialMemoryMethodsMinorityMuscarinic Acetylcholine ReceptorMuscarinicsNeuronal DysfunctionNeuronsNeurotransmitter ReceptorNeurotransmittersNicotinic ReceptorsOutputPatientsPharmaceutical PreparationsProcessPropertyProteinsReceptor ActivationSchizophreniaSliceStimulusStructureSymptomsSynapsesTestingTrainingTransgenic MiceVariantViralbasecholinergiccholinergic neuronextracellularhippocampal pyramidal neuroninformation processinginterestlong term memoryneural information processingneuron lossneuronal cell bodyneurotransmitter releaseoptogeneticspatch clamppresynapticresponseselective expressionsynaptic inhibitionvoltagevoltage/patch clamp
中文摘要
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英文摘要
Project Summary
The long term goal of this project is to have a better understanding of precisely how the release of the
neurotransmitter acetylcholine affects function in a prototypic cortical area of the brain crucially involved in the
formation of long term memories. More specifically, we are interested in how the inputs from an area of the
brain called the medial septum/diagonal band of Broca, (which releases acetylcholine), affects processing of
neural information in an output structure of a cortical area of the brain, (hippocampal CA1), crucial to the
formation of long term memories. These studies will have important implications for developing treatments for
Alzheimer's disease and possibly schizophrenia. The loss of cholinergic neurons that project to cortical
structures in the brain is a hallmark of Alzheimer's disease. Furthermore, drugs that prolong the presence of
acetylcholine in the extracellular space are one of the treatments used to alleviate symptoms in Alzheimer's
patients. Moreover, dysfunction of neuronal nicotinic receptors has been correlated to some familial forms of
schizophrenia. The specific aims for this five year project are to understand how acetylcholine release affects
inhibitory interneuron function and ultimately the processing of information in hippocampal CA1. To do this we
will express a protein called ChIEF in cholinergic neurons that can excite neurons and its processes when
exposed to blue light. This will allow us to elicit the release of acetylcholine in live intact slices of hippocampal
CA1 by merely flashing blue light upon them. We will then examine how acetylcholine release through the
activation of both nicotinic and muscarinic receptors affects interneuron function and ultimately hippocampal
CA1 network function. We will do this by recording electrical responses in interneurons and pyramidal neurons
of hippocampal CA1 via whole cell patch clamp methods, and by recording activity in the entire network by
using voltage-sensitive dye imaging. The results from these studies will have important implications for the
treatment of Alzheimer's disease and some familial forms of schizophrenia.
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依托单位:
海外基金