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Intranasal Insulin Therapy for HIV-Associated Neurocognitive Disorders: Preclinical Evaluation

Intranasal Insulin Therapy for HIV-Associated Neurocognitive Disorders: Preclinical Evaluation
鼻内胰岛素治疗 HIV 相关神经认知障碍:临床前评估
批准号:
9762165
负责人:
Barbara Stauch Slusher
金额:
$23.89万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
已结题
起止时间:
至 2022-05-31
关键词:
Acquired Immunodeficiency SyndromeAffectAlzheimer&aposs DiseaseAnimal ModelAnti-Retroviral AgentsArchivesAttenuatedBehavior assessmentBiological MarkersBrainCellsCharacteristicsChronicCitratesClinical ResearchClinical TrialsCognitiveCognitive deficitsConfocal MicroscopyCreatineDataDiseaseDisease MarkerDoseDrug KineticsEnergy MetabolismFoundationsFunctional disorderFutureGene ExpressionGlutamatesHIVHIV InfectionsHIV therapyHIV-associated neurocognitive disorderHistologicHumanImmunologic Deficiency SyndromesImpaired cognitionIndividualInfectionInflammatoryInsulinInvestigationLinkLipidsMediatingMediator of activation proteinMetabolicMetabolic PathwayMethodsModelingMolecularMolecular ProfilingMonitorMusNeurocognitive DeficitNeurodegenerative DisordersNeurologicNeuronal DysfunctionNeuronsPathogenesisPathway interactionsPatientsPlasmaPreclinical TestingProcessProgram Research Project GrantsProteinsRegimenSeriesSignal PathwaySpleenTestingTissuesTreatment EfficacyVirusabacavirantiretroviral therapybasebrain metabolismbrain tissuechronic infectionclinical investigationcognitive enhancementcognitive processconditioned feardiabeticdiabetic patientdosageeffective therapyexperimental studyimprovedinsightinsulin signalingliquid chromatography mass spectrometrymolecular markermouse modelmyoinositolnervous system disorderneurocognitive testneuroinflammationnovelnovel markerpharmacokinetics and pharmacodynamicspre-clinicalpreclinical evaluationpreventresponseresponse biomarkersuccesstreatment durationvirologywater maze

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PROJECT SUMMARY HAND remains among the most debilitating features of chronic infection with HIV, despite almost universal use of and success of antiretroviral therapy in controlling HIV replication and preventing immunodeficiency and AIDS. The pathophysiological mechanisms of HAND are not well understood, and there are no effective treatments. Growing evidence supports insulin-mediated signaling pathways as key components in normal cognitive processes. Dysregulation of insulin signaling is implicated in inflammatory processes and energy metabolism and associated with the pathogenesis of several neurodegenerative diseases, including HAND. Recent clinical studies have shown that intranasal delivery of insulin to the CNS enhances cognitive processes in normal, Alzheimer’s and diabetic patients. The overall hypothesis of this P01 is that chronic intranasal insulin administration may also be effective in improving cognitive deficits in HAND. In this project we will explore this hypothesis preclinically by testing whether intranasal insulin administration dose dependently increases brain insulin levels, and attenuates cognitive and histological deficits in the EcoHIV murine model of HAND with antivetroviral therapy. We will also monitor energy metabolism, lipid profiles, insulin signaling, and selected markers of neuroinflammation. Collectively these data will provide guidance on the insulin brain exposure and biomarker exploration in the HAND clinical investigations through new information on insulin brain pharmacokinetics and characterization of CSF markers indicative of insulin efficacy. Such exposure-response and biomarker data may prove useful beyond HAND, including future studies in metabolic and other neurodegenerative diseases.
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