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碳-11标记的KF15372:一种潜在的中枢神经系统腺苷A1受体配体。

Carbon-11-labeled KF15372: a potential central nervous system adenosine A1 receptor ligand.

作者信息

Furuta R, Ishiwata K, Kiyosawa M, Ishii S, Saito N, Shimada J, Endo K, Suzuki F, Senda M

机构信息

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

出版信息

J Nucl Med. 1996 Jul;37(7):1203-7.

PMID:8965199
Abstract

UNLABELLED

The carbon-11-labeled selective adenosine A1 antagonist KF15372 ([1-propyl-11C]8-dicyclopropylmethyl-1,3-dipropylxanthine) was elevated in vivo as a PET ligand for mapping CNS adenosine A1 receptors.

METHODS

The regional brain distribution of [11C]KF15372 and the effects of adenosine antagonists on the distribution were determined in mice by tissue sampling. In rats, in which the retinal projection fibres to the superior colliculus had degenerated due to unilateral eye removal, the brain distribution of [11C]KF15372 was visualized by ex vivo autoradiography.

RESULTS

The mouse brain uptake of [11C]KF15372 was 1.8% i.d./g at 5 min and then it gradually decreased. The uptake was high in the hippocampus, cerebral cortex, striatum and cerebellum, and was significantly reduced by A1 antagonists but not by A2 antagonists. The brain distribution of 11C assessed by the tissue sampling and autoradiography was compatible with that of the A1 receptors. Autoradiography clearly visualized unilaterally decreased A1 receptor binding in the superior colliculus.

CONCLUSION

The results demonstrated that [11C]KF15372 is a selective and high-affinity adenosine A1 receptor ligand and is useful for detecting the degeneration of presynaptic neurons.

摘要

未标记

碳-11标记的选择性腺苷A1拮抗剂KF15372([1-丙基-11C]8-二环丙基甲基-1,3-二丙基黄嘌呤)作为用于绘制中枢神经系统腺苷A1受体图谱的正电子发射断层显像(PET)配体在体内得到提升。

方法

通过组织取样在小鼠中测定[11C]KF15372的脑区分布以及腺苷拮抗剂对该分布的影响。在因单侧眼球摘除导致视网膜投射纤维到上丘退化的大鼠中,通过离体放射自显影观察[11C]KF15372的脑分布。

结果

小鼠脑对[11C]KF15372的摄取在5分钟时为1.8%注射剂量/克,然后逐渐下降。在海马体、大脑皮层、纹状体和小脑中摄取较高,且被A1拮抗剂显著降低,但未被A2拮抗剂降低。通过组织取样和放射自显影评估的11C脑分布与A1受体的分布相符。放射自显影清晰显示上丘中单侧A1受体结合减少。

结论

结果表明[11C]KF15372是一种选择性且高亲和力的腺苷A1受体配体,可用于检测突触前神经元的退化。

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