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用正电子发射断层扫描(PET)测量受体占有率。

Measuring receptor occupancy with PET.

作者信息

Waarde A v

机构信息

Positron Emission Tomography (PET) Center, University Hospital Groningen, Groningen, The Netherlands.

出版信息

Curr Pharm Des. 2000 Nov;6(16):1593-610. doi: 10.2174/1381612003398951.

Abstract

Many physiological and biochemical measurements can be performed noninvasively in humans with modern imaging techniques like magnetic resonance imaging (MRI), positron emission tomography (PET) or single-photon emission computed tomography (SPECT). This review focuses on the monitoring of drug-receptor interactions in patients and healthy volunteers with PET. Such studies depend on the availability of a suitable radioligand; they are already possible for classical and atypical neuroleptics, anxiolytics, antidepressants, anticholinergics, antihistamines, antiepileptics, beta-blockers and hypnotic drugs. In Phase I-II human studies, measurements of plasma pharmacokinetics can be combined with images of receptor occupancy and be quantitatively related to pharmacologic effects which are induced in the same subjects. Optimal dosing schedules can be defined and valuable information for the design of Phase III studies can be acquired. Moreover, the effect of interventions (e.g. change of dose, additional medication) can be predicted. Medical imaging techniques will play an increasing role in clinical pharmacology and allow well-informed go/no-go decisions in future drug development.

摘要

借助磁共振成像(MRI)、正电子发射断层扫描(PET)或单光子发射计算机断层扫描(SPECT)等现代成像技术,许多生理和生化测量都可以在人体上进行非侵入性操作。本综述重点关注通过PET对患者和健康志愿者体内药物-受体相互作用的监测。此类研究依赖于合适放射性配体的可用性;对于经典和非典型抗精神病药物、抗焦虑药、抗抑郁药、抗胆碱能药物、抗组胺药、抗癫痫药、β受体阻滞剂和催眠药物,此类研究已经可行。在I-II期人体研究中,血浆药代动力学测量可以与受体占有率图像相结合,并与同一受试者体内诱导产生的药理效应进行定量关联。可以确定最佳给药方案,并获得用于III期研究设计的有价值信息。此外,还可以预测干预措施(如剂量变化、添加药物)的效果。医学成像技术在临床药理学中将发挥越来越重要的作用,并在未来药物开发中做出明智的继续/终止决策。

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