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寻找用于苍白球成像的正电子发射断层显像(PET)探针,并通过大鼠脑离体放射自显影进行研究。

Search for PET probes for imaging the globus pallidus studied with rat brain ex vivo autoradiography.

作者信息

Ishiwata K, Ogi N, Shimada J, Wang W, Ishii K, Tanaka A, Suzuki F, Senda M

机构信息

Positron Medical Center, Tokyo Metropolitan Institute of Gerontology, Itabashi, Japan.

出版信息

Ann Nucl Med. 2000 Dec;14(6):461-6. doi: 10.1007/BF02988292.

Abstract

We have evaluated the feasibility of using four positron emission tomography (PET) tracers for imaging the globus pallidus by ex vivo autoradiography in rats. The tracers investigated were [11C]KF18446, [11C]SCH 23390 and [11C]raclopride for mapping adenosine A2A, dopamine D1 and dopamine D2 receptors, respectively, and [18F]FDG. The highest uptake by the globus pallidus was found for [11C]SCH 23390, followed by [18F]FDG, [11C]KF18446 and [11C]raclopride. The receptor-specific uptake by the globus pallidus was observed in [11C]KF18446 and [11C]SCH 23390, but not in [11C]raclopride. Uptake ratios of globus pallidus to the striatum for [18F]FDG and [11C]KF18446 were approximately 0.6, which was twice as large as that for [11C]SCH 23390. In a rat model of degeneration of striatopallidal gamma-aminobutyric acid-ergic-enkephalin neurons induced by intrastriatal injection of quinolinic acid, the uptake of [11C]KF18446 by the striatum and globus pallidus was remarkably reduced. To prove the visualization of the globus pallidus by PET with [18F]FDG and [11C]KF18446, PET-MRI registration technique and advances in PET technologies providing high-resolution PET scanner will be required. The metabolic activity of the globus pallidus could then be measured by PET with [18F]FDG, and [11C]KF18446 may be a candidate tracer for imaging the pallidal terminals projecting from the striatum.

摘要

我们通过大鼠离体放射自显影评估了使用四种正电子发射断层扫描(PET)示踪剂对苍白球进行成像的可行性。所研究的示踪剂分别为用于绘制腺苷A2A、多巴胺D1和多巴胺D2受体图谱的[11C]KF18446、[11C]SCH 23390和[11C]雷氯必利,以及[18F]氟代脱氧葡萄糖([18F]FDG)。发现苍白球对[11C]SCH 23390的摄取最高,其次是[18F]FDG、[11C]KF18446和[11C]雷氯必利。在[11C]KF18446和[11C]SCH 23390中观察到苍白球的受体特异性摄取,但在[11C]雷氯必利中未观察到。[18F]FDG和[11C]KF18446的苍白球与纹状体摄取比约为0.6,是[11C]SCH 23390的两倍。在通过纹状体内注射喹啉酸诱导的纹状体苍白球γ-氨基丁酸能脑啡肽能神经元变性的大鼠模型中,纹状体和苍白球对[11C]KF18446的摄取显著降低。为了通过[18F]FDG和[11C]KF18446的PET证明苍白球的可视化,将需要PET-MRI配准技术以及提供高分辨率PET扫描仪的PET技术进步。然后可以通过[18F]FDG的PET测量苍白球的代谢活性,并且[11C]KF18446可能是用于对从纹状体投射的苍白球终末进行成像的候选示踪剂。

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