Development of GCPII inhibitors for the treatment of age-related cognitive disorders
Development of GCPII inhibitors for the treatment of age-related cognitive disorders
批准号:
10633273
负责人:
AMY F.T. ARNSTEN
金额:
$78.46万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-09-15 至 2025-05-31
关键词:
AddressAgeAge-associated memory impairmentAgingAgonistAgreementAlzheimer&aposs disease riskBindingBrainBrain DiseasesBrain regionC-terminalCalciumCalcium SignalingCaringChargeChemistryClinicalClinical ResearchCognitionCognitiveCognitive deficitsComputer AssistedCyclic AMPCyclic AMP-Dependent Protein KinasesDataDevelopmentDoseDrug DesignDrug KineticsElderlyExhibitsFOLH1 geneGlutamatesGoalsHealthcareHumanImpaired cognitionIn VitroInflammationLate Onset Alzheimer DiseaseMarylandMediatingMedicalMembraneMemoryMetalloproteasesMonkeysN-acetylaspartateN-acetylaspartylglutamateNeurobiologyNeuronsOralOral AdministrationPermeabilityPersonsPhysiologicalPlayPopulationPotassium ChannelPrefrontal CortexProbabilityProdrugsPublic HealthRattusRegimenRegulationResearch PersonnelResearch ProposalsRisk ReductionRoleSignal TransductionSocietiesSulfhydryl CompoundsTestingTherapeuticTranslatingZincage related cognitive disorderagedaging brainanaloganalog Lassociation cortexclinical candidateclinical translationcognitive enhancementcognitive functioncognitive testingdesigndrug discoveryefficacy studyefficacy testingextracellularimmunogenicityimprovedin vivoinhibitormanufacturemetabotropic glutamate receptors type 3nervous system disorderneuroprotectionnovelnovel strategiesnovel therapeutic interventionpharmacologicpositive allosteric modulatorpostsynapticpre-clinicalresponsescreeningside effectsuccesstau-1translation to humans
中文摘要
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英文摘要
Project Summary
The goal of this research proposal is to develop brain-penetrant inhibitors of glutamate carboxypeptidase II
(GCPII) as a new therapeutic strategy to improve cognition and reduce risk of late-onset Alzheimer's Disease
(AD). GCPII (EC 3.4.17.21) is a membrane-bound zinc metallopeptidase that cleaves the C-terminal
glutamate from N-acetylaspartylglutamate (NAAG) producing N-acetylaspartate and glutamate. NAAG is
known to act as an endogenous agonist at metabotropic glutamate receptor type 3 (mGluR3) and we have
recently found that NAAG can enhance memory-related neuronal firing in monkeys through stimulation of
Gi/Go-mediated regulation of postsynaptic cAMP-PKA-calcium signaling. Therefore, GCPII inhibition may
offer a new therapeutic approach to the cognitive impairments by increasing extracellular NAAG levels and
controlling cAMP-PKA-calcium signaling dysregulated in the aging brain. In the absence of mGluR3-selective
agonists and positive allosteric modulators, this approach is particularly attractive as a number of structurally
diverse and potent GCPII inhibitors have been developed and preclinically evaluated in a variety of
neurological disorders with a robust efficacy and an excellent side effect profile. Indeed, our preliminary data
show cognitive enhancement upon treatment with 2-MPPA, a clinically tested GCPII inhibitor, in aged rats
and monkeys. To date, however, efforts on clinical translation of GCPII inhibitors have been substantially
limited despite the significant therapeutic potential. This prompted us to propose a broad range of
pharmacological approaches to the development of brain-penetrant GCPII inhibitors. We are poised to seize
this therapeutic opportunity for the treatment of age-related cognitive disorders by executing the following
three Specific Aims: (Aim 1) Design and synthesis of GCPII inhibitors and their prodrugs; (Aim 2) Evaluate
the pharmacokinetic (PK) profile of GCPII inhibitors in rats and monkeys; (Aim 3) Assess the effects GCPII
inhibitors on cognitive function in aged rats and monkeys. The successful execution of this project will lead
to a novel therapeutic strategy with greater feasibility for clinical translation to address the main healthcare
needs of the growing elderly population.
期刊论文(4)
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DOI:
10.3390/pharmaceutics14102018
发表时间:
2022-09-23
期刊:
Pharmaceutics
影响因子:
5.4
作者:
[Gori SS, Thomas AG, Pal A, Wiseman R, Ferraris DV, Gao RD, Wu Y, Alt J, Tsukamoto T, Slusher BS, Rais R]
通讯作者:
Rais R
DOI:
10.7150/ntno.63158
发表时间:
2022
期刊:
Nanotheranostics
影响因子:
--
作者:
[Hollinger KR, Sharma A, Tallon C, Lovell L, Thomas AG, Zhu X, Wiseman R, Wu Y, Kambhampati SP, Liaw K, Sharma R, Rojas C, Rais R, Kannan S, Kannan RM, Slusher BS]
通讯作者:
Slusher BS
DOI:
10.3389/fnagi.2021.760270
发表时间:
2021
期刊:
Frontiers in aging neuroscience
影响因子:
4.8
作者:
[Datta D, Leslie SN, Woo E, Amancharla N, Elmansy A, Lepe M, Mecca AP, Slusher BS, Nairn AC, Arnsten AFT]
通讯作者:
Arnsten AFT
DOI:
10.3389/fchem.2022.889737
发表时间:
2022
期刊:
Frontiers in chemistry
影响因子:
5.5
作者:
[]
通讯作者:
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