Ligands and tracers for PET studies of the 5-HT system—current status

C. Crouzel , M. Guillaume , L. Barré , C. Lemaire , V.W. Pike
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引用次数: 57

Abstract

The status of the radiochemical development and biological evaluation of radioligands and tracers for PET studies of the serotonergic system is reviewed, indicating those agents with present value and those with future potential. Practical recommendations are given for the preparation of two useful radioligands for PET studies of central 5-HT2 receptors, namely [18F]setoperone and [18F]altanserin. Though, it has not proved possible to recommend tracers or radioligands for the study of other aspects of the serotonergic system, prospects for future radiochemical development are indicated, especially for developing radioligands for the 5-HT re-uptake site, and for the 5-HT1 and 5-HT3 receptors.

配体和示踪剂用于PET研究5-HT体系的现状
综述了放射性配体和示踪剂在PET研究中用于5 -羟色胺能系统的放射化学发展和生物学评价的现状,指出了具有当前价值和未来潜力的药物。本文给出了用于中央5-HT2受体PET研究的两种有用的放射性配体的制备的实用建议,即[18F]setoperone和[18F]altanserin。虽然目前还不能推荐示踪剂或放射性配体用于5-羟色胺能系统的其他方面的研究,但未来放射化学的发展前景是光明的,特别是开发5-羟色胺再摄取部位的放射性配体,以及5-HT1和5-HT3受体。
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