首页> 外文期刊>Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism >Kinetic analysis of the metabotropic glutamate subtype 5 tracer [18 F]FPEB in bolus and bolus-plus-constant-infusion studies in humans
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Kinetic analysis of the metabotropic glutamate subtype 5 tracer [18 F]FPEB in bolus and bolus-plus-constant-infusion studies in humans

机译:人体推注和推注加常数输注研究中代谢型谷氨酸5型示踪剂[18 F] FPEB的动力学分析

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摘要

[18FF]FPEB is a positron emission tomography tracer which, in preclinical studies, has shown high specificity and selectivity toward the metabotropic glutamate receptor 5 (mGluR5). It possesses the potential to be used in human studies to evaluate mGluR5 function in a range of neuropsychiatric disorders, such as anxiety and Fragile X syndrome. To define optimal scan methodology, healthy human subjects were scanned for 6 hours following either a bolus injection (n=5) or bolus-plus-constant-infusion (n=5) of [1 8F]FPEB. Arterial blood samples were collected and parent fraction measured by high-performance liquid chromatography (HPLC) to determine the metabolite-corrected plasma input function. Time activity curves were extracted from 13 regions and fitted by various models to estimate VT and BPND. [18F]FPEB was well fitted by the two-tissue compartment model, MA1 (t*=30), and MRTM (using cerebellum white matter as a reference). Highest VT values were observed in the anterior cingulate and caudate, and lowest VT values were observed in the cerebellum and pallidum. For kinetic modeling studies, VT and BP ND were estimated from bolus or bolus-plus-constant-infusion scans as short as 90 minutes. Bolus-plus-constant-infusion of [18F]FPEB reduced intersubject variability in VT and allowed equilibrium analysis to be completed with a 30-minute scan, acquired 90-120 minutes after the start of injection.
机译:[18FF] FPEB是一种正电子发射断层扫描示踪剂,在临床前研究中显示出对代谢型谷氨酸受体5(mGluR5)的高特异性和选择性。它具有在人体研究中评估一系列神经精神疾病(例如焦虑症和脆性X综合征)中mGluR5功能的潜力。为定义最佳扫描方法,在推注(1 = 8F)FPEB的大剂量推注(n = 5)或推注加恒定输注(n = 5)之后,对健康的人类受试者进行了6小时的扫描。收集动脉血样品,并通过高效液相色谱(HPLC)测量母体成分,以确定代谢物校正的血浆输入功能。从13个区域提取时间活动曲线,并通过各种模型拟合以估计VT和BPND。 [18F] FPEB非常适合两组织隔室模型,MA1(t * = 30)和MRTM(以小脑白质为参考)。在前扣带回和尾状核中观察到最高的VT值,在小脑和苍白质中观察到最低的VT值。对于动力学模型研究,可从短短90分钟的推注或推注加恒定输注扫描中估算出VT和BP ND。持续加注Bolus加[18F] FPEB可减少受试者之间的室速变异性,并允许在注射开始90-120分钟后进行30分钟扫描以完成平衡分析。

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