Development of E64d for Alzheimer's disease
Development of E64d for Alzheimer's disease
批准号:
8318932
负责人:
GREGORY R HOOK
金额:
$5.85万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-30 至 2013-02-28
关键词:
AcidsActive SitesAlzheimer&aposs DiseaseAmyloid beta-Protein PrecursorAnimal ExperimentsAnimal ModelAnimalsAssesBehaviorBindingBiological AvailabilityBiological MarkersBloodBlood - brain barrier anatomyBlood VesselsBrainCarotid ArteriesCathepsins BCattleCaviaChildChromaffin CellsCleaved cellClinicalClinical ResearchClinical TrialsCollaborationsCyclodextrinsCysteine ProteaseCysteine Proteinase InhibitorsDataDevelopmentDimethyl SulfoxideDiseaseDisease ProgressionDoseDouble-Blind MethodDrug FormulationsDrug KineticsEstersEvaluationExcipientsExpressed Sequence TagsFundingGoalsGovernmentGrantHealthHepaticHousingHumanInfusion proceduresInjection of therapeutic agentIntravenousJapanJapanese PopulationJournalsKidneyLabelLiverLondonMeasuresMemory impairmentModelingMonkeysMusMuscular DystrophiesMutationNoseOralOral AdministrationPaperPathologyPathway interactionsPatientsPenetrationPeptide HydrolasesPersonsPharmaceutical PreparationsPharmacologic SubstancePhaseProceduresProdrugsProductionPublic HealthPublishingResearchRouteSecretory VesiclesSenile PlaquesSiteSocial WelfareSolutionsSulfhydryl CompoundsTestingTherapeuticTissuesToxicologyTransgenic MiceTransgenic OrganismsTranslatingWorkamyloid peptidebasecost effectiveimprovedin vivoinhibitor/antagonistmalemorris water mazemouse modelneurotoxicpeptide Apre-clinicalprogramsresearch studyresponsesecretasetransgenic model of alzheimer diseaseuptakevolunteeryoung adult
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): There currently is no drug available that stops the progression of Alzheimer's disease (AD). The abnormal accumulation of neurotoxic brain ss-amyloid peptides (A?) is thought to be a possible cause the disease. A? are produced by proteolytic cleavage of a larger amyloid precursor protein by proteases, called ?- and ?-secretases. Inhibiting 2-secretase cleavage is an attractive approach to reducing A? accumulation and ?-secretase inhibitors are thought to potentially effective for slowing the progression of the disease. We have found a compound, E64d, which improves spatial memory deficit and reduces brain plaque, A? and CTF? in a transgenic AD mouse when intracerebroventricularly (icv) administered. Moreover, E64d also reduces brain A? in the regulated secretory pathway in the guinea pig model of human A? production. The reduction in CTF? and A? in the regulated secretory pathway suggests that E64d may act by inhibiting ?-secretase activity in that pathway. Previously, others found that oral E64d administration safe to use in clinical trials. Thus, E64d is both efficacious in AD animal models and safe to use in humans and therefore has potential as an AD therapeutic. E64d is an ester prodrug of its biologically active acid form, E64c, which is a specific inhibitor of cysteine proteases. E64d is rapidly hydrolyzed to E64c in vivo. However, icv E64d administration is not a therapeutically acceptable route and oral E64d administration results in low brain doses, which is due to hepatic E64c uptake prior to reaching the brain. Therapeutically acceptable and efficacious routes of E64d administration need to be developed in order to advance E64d as an AD therapeutic. This grant will explore various routes of E64d administration and determine their efficacy and brain dose responses in AD animal models. If a suitable route is found, this work will allow the clinical development of a very promising AD therapeutic to proceed. PUBLIC HEALTH RELEVANCE: The relevance of this project to the public health is the development of new and effective Alzheimer's disease drug. Currently, there is no effective means of stopping the progress of this devastating disease and there is an urgent need for new drugs that do so. This project may result in a new Alzheimer's disease treatment that may halt or, possibly, reverse the progression of the disease.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI:
10.3233/jad-131370
发表时间:
2014
期刊:
Journal of Alzheimer's disease : JAD
影响因子:
--
作者:
[Hook G, Yu J, Toneff T, Kindy M, Hook V]
通讯作者:
Hook V
Administrative Supplement to restore fee funds
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批准号:9982655
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项目类别:
-
资助金额:$3.62万
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财政年份:2019
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负责人:GREGORY R HOOK
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依托单位:
Development of protease inhibitor drugs to treat Alzheimer's disease
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批准号:7935012
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项目类别:
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资助金额:$19.6万
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财政年份:2009
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负责人:GREGORY R HOOK
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依托单位:
Prodrugs to treat Alzheimer's disease
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批准号:7762713
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项目类别:
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资助金额:$10.16万
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财政年份:2009
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负责人:GREGORY R HOOK
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依托单位:
Development of E64d for Alzheimer's disease
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批准号:7767386
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项目类别:
-
资助金额:$56.72万
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财政年份:2008
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负责人:GREGORY R HOOK
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依托单位:
Development of protease inhibitor drugs to treat Alzheimer's disease
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批准号:7477514
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项目类别:
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资助金额:$9.51万
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财政年份:2008
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负责人:GREGORY R HOOK
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依托单位:
Development of E64d for Alzheimer's disease
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批准号:7541167
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项目类别:
-
资助金额:$11.51万
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财政年份:2008
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负责人:GREGORY R HOOK
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依托单位:
Development of protease inhibitor drugs to treat Alzheimer's disease
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批准号:7743874
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项目类别:
-
资助金额:$42.75万
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财政年份:2008
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负责人:GREGORY R HOOK
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依托单位:
Inhibitors of beta-Amyloid Production in Alzheimer's
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批准号:7142250
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项目类别:
-
资助金额:$16.32万
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财政年份:2006
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负责人:GREGORY R HOOK
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依托单位:
Inhibitors of beta-Amyloid Production in Alzheimer's
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批准号:7286818
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项目类别:
-
资助金额:$15.85万
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财政年份:2006
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负责人:GREGORY R HOOK
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依托单位:
Gamma Secretase Assays to Discover Drugs for Alzheimer's
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批准号:7101003
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项目类别:
-
资助金额:$80.84万
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财政年份:2000
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负责人:GREGORY R HOOK
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依托单位:
GAMMA SECRETASE ASSAYS FOR DRUG DISCOVERY IN ALZHEIMER'S
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批准号:6137076
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项目类别:
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资助金额:$10.0万
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财政年份:2000
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负责人:GREGORY R HOOK
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依托单位:
Gamma Secretase Assays to Discover Drugs for Alzheimer's
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批准号:6989920
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项目类别:
-
资助金额:$76.33万
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财政年份:2000
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负责人:GREGORY R HOOK
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依托单位:
SECRETASE ASSAYS TO DISCOVER DRUGS TO TREAT ALZHEIMER'S
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批准号:6017363
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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:1999
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负责人:GREGORY R HOOK
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依托单位:
Beta-Secretase Assays to Discover Drugs for Alzheimer's
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批准号:6742470
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项目类别:
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资助金额:$37.9万
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财政年份:1999
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负责人:GREGORY R HOOK
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依托单位:
Beta-Secretase Assays to Discover Drugs for Alzheimer's
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批准号:6717501
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项目类别:
-
资助金额:$40.12万
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财政年份:1999
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负责人:GREGORY R HOOK
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依托单位:
Beta-Secretase Assays to Discover Drugs for Alzheimer's
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批准号:6442643
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项目类别:
-
资助金额:$31.58万
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财政年份:1999
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负责人:GREGORY R HOOK
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依托单位:
Beta-Secretase Assays to Discover Drugs for Alzheimer's
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批准号:6622206
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项目类别:
-
资助金额:$59.8万
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财政年份:1999
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负责人:GREGORY R HOOK
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依托单位:
海外基金