Icariin to Prevent Corticosteroid-Related Memory Changes
Icariin to Prevent Corticosteroid-Related Memory Changes
批准号:
8490143
负责人:
E SHERWOOD BROWN
金额:
$22.66万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-09-30 至 2015-08-31
关键词:
Activated Partial Thromboplastin Time measurementAdrenal Cortex HormonesAdverse effectsAngiospermsAnimal ModelAnimalsAntidepressive AgentsAnxietyAphrodisiacsApoptosisArthritisAsiaAsthmaAttenuatedBehaviorBerberidaceaeBipolar DisorderBrainBrain DiseasesBrain regionChinese HerbsClinical PharmacologyClinical ResearchCognitionCognitiveCollaborationsControlled Clinical TrialsCross-Over StudiesDataDoseDouble-Blind MethodDrug KineticsEpimediumErectile dysfunctionExposure toFamilyFlavonoidsFrequenciesFutureGlucocorticoidsGlutamatesGoalsHalf-LifeHealth SciencesHemorrhageHerbal MedicineHippocampus (Brain)HormonesHumanHydrocortisoneIschemiaLaboratoriesMajor Depressive DisorderManicMeasuresMedicalMemoryMemory impairmentMental DepressionModelingMonitorMood DisordersMoodsN-Methyl-D-Aspartate ReceptorsNeuraxisNeuronsOrganOutcome MeasurePatient Self-ReportPatientsPerformancePharmaceutical PreparationsPharmacy SchoolsPhasePilot ProjectsPlacebo ControlPlacebosPlantsPopulationPrednisonePropertyProthrombinPublishingRattusReportingResearchRiskSafetySecondary toShort-Term MemoryStressStructureSymptomsTestingTexasTherapeuticTimeTransplantationUniversitiesWomanWorkbasebone losscontrol trialdesignexperienceflavanoidhippocampal atrophyhypomaniaimprovedinhibitor/antagonistneuroprotectionphosphoric diester hydrolasepre-clinicalpreventprimary outcomeprogramspublic health relevanceresearch study
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): In animals and humans, stress and corticosteroid excess are associated with changes in hippocampal structure and functioning. These findings have important implications for 1) patients with mood disorders, because subsets of people with major depressive disorder and bipolar disorder have elevated cortisol and memory impairment, and 2) the estimated 1% of the population treated with prescription corticosteroids for medical illnesses. Icariin, a flavonoid from Epimedium, 1) blocks the effects of corticosteroid-induced apoptosis in primary cultured rat hippocampal neurons, 2) is neuroprotective in animal models of ischemia, 3) improves memory in animal models of cognition, and 4) has antidepressant properties in an animal model of depression. Despite these promising pre-clinical findings, and the widespread availability of icariin in over-the-counter supplements, no studies have examined the effects of this compound on the human brain or examined its pharmacokinetics in humans. Only one human controlled trial of icariin has been reported, to date. In this report icariin appeared to be safe, well tolerated and effective when given to women for bone loss. Our group has a research program using patients in medical settings receiving prescription corticosteroid (e.g. prednisone) therapy or healthy controls receiving brief corticosteroid exposures in a laboratory paradigm as models to explore the effects of cortisol elevations on the human brain. A major current focus of our work is on medications that may block the effects of stress or corticosteroids on the hippocampus (a brain region essential for memory). We have identified several promising agents. We propose to explore whether icariin will block the effects of hydrocortisone (cortisol) on memory in healthy controls. The current proposal has two phases. In Phase I the pharmacokinetics of icariin, and the safety and tolerability of two icariin doses wil be assessed. This will provide needed data for the second phase of this proposal, and for other future human research with icariin. In Phase II we will determine whether icariin blocks the effects of corticosteroids on memory using our paradigm. This experiment will examine icariin both alone and in combination with hydrocortisone in healthy controls using a battery of cognitive tests and mood assessments. Safety and tolerability will also be monitored. A highly experienced research team that has completed and published studies with similar designs as in the current proposal will conduct the project.
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T35 NIAAA Summer Research Program
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Dopamine-2 Receptor Partial Agonist for Bipolar Disorder and Alcohol Use Disorder
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Clinical Medication Development for Bipolar Disorder and Alcohol Use Disorders
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财政年份:2015
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Citicoline for Alcohol Dependence
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依托单位:
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依托单位:
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Attenuation of Corticosteroid-Induced Hippocampal Changes
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项目类别:
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依托单位: