Selection, design and evaluation of new radioligands for PET studies of cardiac adrenoceptors

V.W Pike , M.P Law , S Osman , R.J Davenport , O Rimoldi , D Giardinà , P.G Camici
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引用次数: 27

Abstract

Changes in the numbers of human cardiac adrenoceptors (ARs) are associated with various diseases, such as myocardial ischemia, congestive heart failure, cardiomyopathy and hypertension. There is a clear need for capability to assess human cardiac ARs directly in vivo. Positron emission tomography (PET) is an imaging technique that provides this possibility, if effective radioligands can be developed for the targeted ARs. Here, the status of myocardial AR radioligand development for PET is described. Currently, there exist effective radioligands for imaging β-ARs in human myocardium. One of these, [11C](S)-CGP 12177, is applied extensively to clinical research with PET, sometimes with other tracers of other aspects of the noradrenalin system. Alternative radioligands are in development for β-ARs, including β1-selective radioligands. A promising radioligand for imaging myocardial α1-ARs, [11C]GB67, is now being evaluated in human PET experiments.

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用于心脏肾上腺素受体PET研究的新型放射配体的选择、设计和评价
人心脏肾上腺素受体(ARs)数量的变化与多种疾病有关,如心肌缺血、充血性心力衰竭、心肌病和高血压。显然需要能够直接在体内评估人类心脏ARs的能力。正电子发射断层扫描(PET)是一种成像技术,提供了这种可能性,如果有效的放射性配体可以为目标ARs开发。本文描述了心肌AR放射配体在PET中的发展状况。目前,已有有效的β- ar成像放射配体存在于人心肌中。其中一种[11C](S)-CGP 12177广泛应用于PET临床研究,有时与去甲肾上腺素系统其他方面的其他示踪剂一起应用。β- ar的替代放射配体正在开发中,包括β1选择性放射配体。一种很有前途的用于心肌α1-ARs成像的放射配体[11C]GB67,目前正在人体PET实验中进行评估。
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