Bergström K A, Halldin C, Kuikka J T, Swahn C G, Tiihonen J, Hiltunen J, Länsimies E, Farde L
Department of Clinical Physiology and Nuclear Medicine, Kuopio University Hospital, Finland.
Synapse. 1995 Apr;19(4):297-300. doi: 10.1002/syn.890190407.
I-123 or C-11 labelled 2 beta-carbomethoxy-3 beta-(4-iodophenyl)tropane (beta-CIT) is a recently developed radioligand for the study of dopamine and serotonin reuptake sites in humans with single photon emission tomography (SPET) or positron emission tomography (PET). Determination of the radioligand metabolite pattern is fundamental for a quantitative analysis of radioligand binding. The metabolism of [123I]beta-CIT was determined by a gradient HPLC method in plasma samples of six human subjects. Two metabolites of [123I]beta-CIT were found, a polar and a lipophilic. At 4 h after [123I]beta-CIT injection the percentages of parent compound and polar and lipophilic metabolites were 23 +/- 3% (mean +/- SD), 33 +/- 11%, and 44 +/- 8%, respectively. The lipophilic metabolite might pass the blood-brain barrier and account for a fraction of free and nonspecifically bound radioactivity in brain. The existence of a lipophilic metabolite of [123I]beta-CIT may obstruct the use of simple ratio methods for quantitation of the dopamine transporter in brain.
I - 123或C - 11标记的2β - 甲氧基羰基 - 3β - (4 - 碘苯基)托烷(β - CIT)是一种最近开发的放射性配体,用于通过单光子发射断层扫描(SPET)或正电子发射断层扫描(PET)研究人体中的多巴胺和5 - 羟色胺再摄取位点。确定放射性配体代谢物模式对于放射性配体结合的定量分析至关重要。采用梯度高效液相色谱法测定了6名人类受试者血浆样本中[123I]β - CIT的代谢情况。发现了[123I]β - CIT的两种代谢物,一种极性代谢物和一种亲脂性代谢物。在注射[123I]β - CIT后4小时,母体化合物、极性代谢物和亲脂性代谢物的百分比分别为23±3%(平均值±标准差)、33±11%和44±8%。亲脂性代谢物可能会穿过血脑屏障,并在脑中占一部分游离和非特异性结合的放射性。[123I]β - CIT亲脂性代谢物的存在可能会妨碍使用简单的比值法对脑中多巴胺转运体进行定量分析。