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正电子发射断层扫描(PET)成像示踪剂用于血清素受体。

Positron Emission Tomography (PET) Imaging Tracers for Serotonin Receptors.

机构信息

Key Laboratory of Radiopharmaceuticals, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing 100875, China.

Division of Nuclear Medicine and Molecular Imaging, Massachusetts General Hospital, Boston, Massachusetts 02114, United States.

出版信息

J Med Chem. 2022 Aug 25;65(16):10755-10808. doi: 10.1021/acs.jmedchem.2c00633. Epub 2022 Aug 8.

Abstract

Serotonin (5-hydroxytryptamine, 5-HT) and 5-HT receptors (5-HTRs) have crucial roles in various neuropsychiatric disorders and neurodegenerative diseases, making them attractive diagnostic and therapeutic targets. Positron emission tomography (PET) is a noninvasive nuclear molecular imaging technique and is an essential tool in clinical diagnosis and drug discovery. In this context, numerous PET ligands have been developed for "visualizing" 5-HTRs in the brain and translated into human use to study disease mechanisms and/or support drug development. Herein, we present a comprehensive repertoire of 5-HTR PET ligands by focusing on their chemotypes and performance in PET imaging studies. Furthermore, this Perspective summarizes recent 5-HTR-focused drug discovery, including biased agonists and allosteric modulators, which would stimulate the development of more potent and subtype-selective 5-HTR PET ligands and thus further our understanding of 5-HTR biology.

摘要

血清素(5-羟色胺,5-HT)和 5-羟色胺受体(5-HTRs)在各种神经精神疾病和神经退行性疾病中起着至关重要的作用,使它们成为有吸引力的诊断和治疗靶点。正电子发射断层扫描(PET)是一种非侵入性核分子成像技术,是临床诊断和药物发现的重要工具。在这方面,已经开发了许多 PET 配体来“可视化”大脑中的 5-HTR,并转化为人类使用,以研究疾病机制和/或支持药物开发。在此,我们通过关注其化学型和在 PET 成像研究中的表现,呈现了一套全面的 5-HTR PET 配体。此外,本观点总结了最近以 5-HTR 为重点的药物发现,包括偏性激动剂和变构调节剂,这将刺激更有效和亚型选择性的 5-HTR PET 配体的开发,从而进一步了解 5-HTR 生物学。

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