Anti-oxidant therapy in Alzheimer's disease
Anti-oxidant therapy in Alzheimer's disease
批准号:
7569490
负责人:
Brian J Bacskai
金额:
$26.14万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-02-15 至 2010-12-31
关键词:
AcuteAdvanced Glycosylation End ProductsAlzheimer&aposs DiseaseAmyloidAntioxidantsApoptosisApplications GrantsBiological AssayBrainChronicClinical TrialsDetectionDiseaseEffectivenessFluorescenceFluorescent ProbesFree RadicalsGenerationsGinkgo biloba extractGliosisImageImaging TechniquesIn VitroLifeLigandsMeasuresMediatingMicroscopyMonitorNeurologicNeuronal DysfunctionNeuronsOutcome MeasureOxidative StressPathogenesisPatientsPeptidesReactive Oxygen SpeciesReaderReporterResearch PersonnelSenile PlaquesSorting - Cell MovementSourceSpectrum AnalysisStressStructureSynapsesTechniquesTestingTissuesToxic effectTransgenic MiceVitamin Eantioxidant therapybasebrain tissueeffective therapyfunctional outcomesgrape seed extracthigh throughput screeningin vivomouse modeloxidationoxidative damageperoxidationpreventtherapeutic target
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Alzheimer's disease (AD) is a devastating neurological illness with no known cure, yet a central hypothesis
implicating oxidative stress as a cause of the disease has been postulated for more than a decade. AD is
characterized in post-mortem tissue by the presence of senile plaques that result from the progressive brain
accumulation of amyloid-p (A(3)peptides; thus Ap is the principle therapeutic target for treating AD. There
are numerous studies with anti-oxidant therapy, however none examine the AD-specific contribution
quantitatively. Clinical trials with anti-oxidant therapy have have also shown limited efficacy. Our approach
provides quantitative readouts of AD-specific oxidative stress to optimize an anti-oxidant treatment. While
we have shown that oxidative stress results from the senile plaques of AD themselves, it is likely that other
p species, such as small diffusible aggregates, oligpmers, or Ap derived diffusible ligands (ADDLs) are also
a source of reactive oxygen species. This grant application proposes to identify aggregated and soluble Ap
components that are sources of oxidative stress, and evaluate anti-oxidant treatments for protective activity
both in vitro and in vivo using transgenic mouse models of AD. Our strength lies in the utilization of.
sophisticated imaging techniques based on multiphoton microscopy that allow us to image senile plaques
structurally and functionally in vitro and in vivo. Small diffusible aggregates of Ap like oligomers and ADDLs
can be analyzed and characterized using high-throughput plate-reader assays or multiphoton fluorescence
correlation spectroscopy (PCS). Anti-oxidants can be tested for their ability to reduce or prevent the
oxidative stress resulting from these small toxic Ap species. In combination, these experimental paradigms
will be used to screen potential anti-oxidants from both traditional and alternative sources to systematically
evaluate whether compounds like ginkgo biloba extract, vitamin E, or grape seed extract are effective anti-
oxidants for Alzheimer's disease treatment. The results will bridge the gap between the description of
oxidative stress in Alzheimer's disease to direct determination of the anti-oxidant ability of natural and
synthetic products that should hold promise for treatment of AD patients.
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会议论文
Slow-wave activity as a modifier of the progression of neurodegeneration in Alzheimer's disease
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批准号:10657937
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项目类别:
-
资助金额:$127.22万
-
财政年份:2019
-
负责人:Brian J Bacskai
-
依托单位:
Slow-wave activity as a modifier of the progression of neurodegeneration in Alzheimer's disease
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批准号:10205286
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项目类别:
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资助金额:$19.5万
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财政年份:2019
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负责人:Brian J Bacskai
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依托单位:
Astrocytes as governing pathological drivers of neurovascular dysfunction in AD
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批准号:10584240
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项目类别:
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资助金额:$53.41万
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财政年份:2017
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负责人:Brian J Bacskai
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依托单位:
CEREBRAL AMYLOID ANGIOPATHY AND MECHANISMS OF BRAIN AMYLOID ACCUMULATION
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批准号:9884824
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项目类别:
-
资助金额:$113.43万
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财政年份:2016
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负责人:Brian J Bacskai
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依托单位:
Molecular pathways leading to neurodegeneration in vivo
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批准号:9472989
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项目类别:
-
资助金额:$46.73万
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财政年份:2015
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负责人:Brian J Bacskai
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依托单位:
Molecular pathways leading to neurodegeneration in vivo
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批准号:8887495
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项目类别:
-
资助金额:$50.67万
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财政年份:2015
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负责人:Brian J Bacskai
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依托单位:
A replacement multiphoton microscope for in vivo imaging in rodent models of neur
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批准号:7595490
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项目类别:
-
资助金额:$49.15万
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财政年份:2009
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负责人:Brian J Bacskai
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依托单位:
MULTIPHOTON MICROSCOPY FOR IN VIVO NEURAL IMAGING
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批准号:7563694
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项目类别:
-
资助金额:$0.61万
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财政年份:2007
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负责人:Brian J Bacskai
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依托单位:
Non-invasive optical imaging of neuropathology in vivo
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批准号:7903375
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项目类别:
-
资助金额:$84.22万
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财政年份:2006
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负责人:Brian J Bacskai
-
依托单位:
Anti-oxidant therapy in Alzheimer's disease
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批准号:7185057
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项目类别:
-
资助金额:$26.67万
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财政年份:2006
-
负责人:Brian J Bacskai
-
依托单位:
Anti-oxidant therapy in Alzheimer's disease
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批准号:7794971
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项目类别:
-
资助金额:$25.88万
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财政年份:2006
-
负责人:Brian J Bacskai
-
依托单位:
Anti-oxidant therapy in Alzheimer's disease
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批准号:7365118
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项目类别:
-
资助金额:$26.14万
-
财政年份:2006
-
负责人:Brian J Bacskai
-
依托单位:
Anti-oxidant therapy in Alzheimer's disease
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批准号:7032562
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项目类别:
-
资助金额:$27.47万
-
财政年份:2006
-
负责人:Brian J Bacskai
-
依托单位:
Non-invasive optical imaging of neuropathology in vivo
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批准号:7071532
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项目类别:
-
资助金额:$86.68万
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财政年份:2006
-
负责人:Brian J Bacskai
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依托单位:
Non-invasive optical imaging of neuropathology in vivo
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批准号:7282428
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项目类别:
-
资助金额:$79.26万
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财政年份:2006
-
负责人:Brian J Bacskai
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依托单位:
Non-invasive optical imaging of neuropathology in vivo
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批准号:7662441
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项目类别:
-
资助金额:$82.54万
-
财政年份:2006
-
负责人:Brian J Bacskai
-
依托单位:
Non-invasive optical imaging of neuropathology in vivo
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批准号:7474007
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项目类别:
-
资助金额:$80.08万
-
财政年份:2006
-
负责人:Brian J Bacskai
-
依托单位:
Mechanisms of amyloid-beta clearance.
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批准号:7006068
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项目类别:
-
资助金额:$28.09万
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财政年份:2003
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负责人:Brian J Bacskai
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依托单位:
Mechanisms of amyloid-beta clearance.
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批准号:6837618
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项目类别:
-
资助金额:$28.76万
-
财政年份:2003
-
负责人:Brian J Bacskai
-
依托单位:
Mechanisms of amyloid-beta clearance.
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批准号:6698814
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项目类别:
-
资助金额:$28.76万
-
财政年份:2003
-
负责人:Brian J Bacskai
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依托单位:
海外基金