Can [18F]3F4AP detect brain demyelination? Evaluation of novel PET tracer in nonhuman primates and humans
Can [18F]3F4AP detect brain demyelination? Evaluation of novel PET tracer in nonhuman primates and humans
批准号:
10322678
负责人:
Pedro Brugarolas
金额:
$36.28万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-12-15 至 2024-11-30
关键词:
4-AminopyridineAlzheimer&aposs DiseaseAnimal ModelArchitectureAreaAxonBindingBiochemicalBlood - brain barrier anatomyBlood specimenBrainBrain IschemiaBrain imagingClinicalClinical ResearchComplementCraniotomyData AnalysesDemyelinating DiseasesDemyelinationsDiagnosisDiseaseDrug usageEvaluationFDA approvedFiberFutureGeneticGoalsHistologicHumanImageImaging DeviceImmunologicsInflammationInjuryKineticsLesionMacaca mulattaMagnetic Resonance ImagingMeasuresMetabolicMetabolismMethodsMinorModelingMonitorMonkeysMotorMultiple SclerosisMyelinMyelin SheathNeuraxisNeurobehavioral ManifestationsNeuronsNutrientPathologic ProcessesPenetrationPerformancePharmaceutical PreparationsPositron-Emission TomographyPotassium ChannelPrimatesProceduresProcessPropertyRattusRodentRodent ModelRoleScanningSensorySeverity of illnessSignal TransductionSpeedSpinal cord injuryStrokeTarget PopulationsTestingTimeTracerTraumatic Brain InjuryVoltage-Gated Potassium ChannelWalkingWaterbasedesignexperimental studyfirst-in-humanimaging propertiesinjuredkinetic modelleukodystrophymicroPETnonhuman primatenormal agingnoveloverexpressionquantitative imagingradioligandradiotracerremyelinationtherapy development
中文摘要
项目摘要
脱髓鞘是多发性硬化症的标志,在其他疾病中也存在。
包括脑缺血、创伤性脑损伤,甚至阿尔茨海默病。目前,脱髓鞘
疾病主要是使用核磁共振成像。尽管mri对脱髓鞘高度敏感,但它不是。
它是定量的,不能区分脱髓鞘和其他潜在的共同存在的病理过程
如炎症或轴突丢失。正电子发射断层扫描(PET)可以提供定量和
生物化学的特定信息来补充核磁共振。
我们最近基于FDA批准的治疗MS 4的药物开发了一种用于脱髓鞘的PET放射性示踪剂。
氨基吡啶(4AP),又称[18F]3F4AP。我们发现这种示踪剂可以用来检测啮齿动物的脱髓鞘。
多发性硬化症的模型,它有良好的性质,以成像猴子的大脑。在这个项目中,我们寻求
研究这种示踪剂在创伤性脑损伤模型中脱髓鞘成像的潜力,并
在非人类灵长类动物和人类身上进行验证。这里收集的信息将对设计和
对未来人类研究的解释。一旦得到验证,该示踪剂将有助于更好地监测
对脱髓鞘疾病和逆转脱髓鞘疗法的发展作出了贡献。
英文摘要
Project Summary
Demyelination represents the hallmark of multiple sclerosis (MS) and is also present in other diseases
including brain ischemia, traumatic brain injury and even Alzheimer’s disease. Currently, demyelinating
diseases are primarily imaged using MRI. Even though MRI is highly sensitive to demyelination, it is not
quantitative and it cannot distinguish demyelination from other potentially coexisiting pathological processes
such as inflammation or axonal loss. Positron Emission Tomography (PET) can provide quantitative and
biochemically specific information to complement MRI.
We recently developed a PET radiotracer for demyelination based on the FDA-approved drug for MS 4-
aminopyridine (4AP) called [18F]3F4AP. We showed that this tracer be used to detect demyelination in rodent
models of MS and that it has good properties for imaging the brain in monkeys. In this project, we seek to
investigate the potential of this tracer for imaging demyelination in a model of traumatic brain injury and to
validate it in nonhuman primates and humans. The information gathered here will be crucial for the design and
interpretation of future human studies. Once validated, this tracer and could contribute to better monitoring of
demyelinating diseases and to the development of therapies to reverse demyelination.
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Can [18F]3F4AP detect brain demyelination? Evaluation of novel PET tracer in nonhuman primates and humans
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批准号:10528483
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项目类别:
-
资助金额:$36.28万
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财政年份:2019
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负责人:Pedro Brugarolas
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依托单位:
New tools for imaging: diagnostics based on therapeutics
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批准号:9102100
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项目类别:
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资助金额:$8.37万
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财政年份:2015
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负责人:Pedro Brugarolas
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依托单位: