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首页> 外文期刊>Nuclear Medicine and Biology >[F-18]desmethoxyfallypride as a novel PET radiotracer for quantitative in vivo dopamine D2/D3 receptor imaging in rat models of neurodegenerative diseases
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[F-18]desmethoxyfallypride as a novel PET radiotracer for quantitative in vivo dopamine D2/D3 receptor imaging in rat models of neurodegenerative diseases

机译:[F-18] desmethoxyfallypride作为新型PET放射性示踪剂,用于神经退行性疾病大鼠模型中体内多巴胺D2 / D3受体定量成像

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Introduction: [F-18]desmethoxyfallypride ([F-18]DMFP) is a promising tracer for longitudinal assessment of striatal dopamine D2/D3-receptor (D2R) availability by positron emission tomography (PET) in small animal models. We explored the feasibility of [F-18]DMFP-PET to image D2R availability in rat models of Huntington's (HD) and Parkinson's disease (PD).
机译:简介:[F-18]去甲氧基fallypride([F-18] DMFP)是一种有希望的示踪剂,可通过正电子发射断层扫描(PET)在小动物模型中纵向评估纹状体多巴胺D2 / D3-受体(D2R)的有效性。我们探讨了[F-18] DMFP-PET在亨廷顿病(HD)和帕金森氏病(PD)大鼠模型中对D2R可用性进行成像的可行性。

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