Brain radioligands -: State of the art and new trends

被引:0
|
作者
Halldin, C [1 ]
Gulyás, B [1 ]
Langer, O [1 ]
Farde, L [1 ]
机构
[1] Karolinska Inst, Karolinska Hosp, Dept Clin Neurosci, Psychiat Sect, S-17176 Stockholm, Sweden
来源
QUARTERLY JOURNAL OF NUCLEAR MEDICINE | 2001年 / 45卷 / 02期
关键词
tomography; emission computed; single photon radiopharmaceuticals; brain; carbon radioisotopes; fluorine radioisotopes;
D O I
暂无
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Non-invasive radioligand imaging methods for brain receptor studies use either short-lived positron-emitting radionuclides such as C-11 and F-18 for positron emission tomography (PET) or single photon-emitting radionuclides such as I-123 for single photon emission computed tomography (SPECT). PET and SPECT use radioligands which are injected intravenously into experimental animals, human volunteers or patients. The main applications of radioligands in brain research concern human neuropsychopharmacology and the discovery and development of novel drugs to be used in the therapy of neurological and psychiatric disorders. A basic problem in PET and SPECT brain receptor studies is the lack of useful radioligands with appropriate binding characteristics. Prerequisite criteria need to be satisfied for a radioligand to reveal target binding sites in vivo. This section will discuss these important criteria and also review recent examples in neuroreceptor radioligand development such as selective radioligands for brain monoamine transporters.
引用
收藏
页码:139 / 152
页数:14
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