Rabiner Eugenii A, Messa Cristina, Sargent Peter A, Husted-Kjaer Karen, Montgomery Andrew, Lawrence Andrew D, Bench Christopher J, Gunn Roger N, Cowen Phillip, Grasby Paul M
MRC Cyclotron Unit, Division of Neuroscience and Psychological Medicine, Imperial College School of Medicine, Hammersmith Hospital, London W12 0NN, United Kingdom.
Neuroimage. 2002 Mar;15(3):620-32. doi: 10.1006/nimg.2001.0984.
PET studies of [(11)C]WAY-100635 binding are proving to be a useful tool to evaluate 5-HT(1A) receptor function in vivo in humans. We describe the pattern of [(11)C]WAY-100635 binding in 61 healthy male brains and examine its variability. For all PET scans, binding potential (BP) values for [(11)C]WAY-100635 in different regions were calculated using a simplified reference tissue model, with the cerebellum as reference region. Specifically we describe (1) region of interest and SPM databases of PET [(11)C]WAY-100635 binding, including test-retest variability; (2) the sensitivity of [(11)C]WAY-100635 binding to manipulations of endogenous 5-HT; and (3) correlations between [(11)C]WAY-100635 binding and radiochemical, demographic, physiological, and behavioral variables. The regional distribution of [(11)C]WAY-100635 binding in healthy human brain was similar to that reported in vitro. The test-retest variability was approximately 12% (range 9-16%) and was similar for all methods of regional sampling. The binding of [(11)C]WAY-100635 was insensitive to changes in brain 5-HT induced by tryptophan infusion and depletion. Although BP values varied greatly across subjects (range 2.9-6.8), there were no significant correlations of regional and global BP with common radiochemical, demographic, physiological, and personality variables. Specifically, in contrast with two recent small studies, we found no decline of [(11)C]WAY-100635 binding with age in our large cohort over the age range of 24 to 53 years. Assessment of 5-HT(1A) receptors in vivo using PET and [(11)C]WAY-100635 gives reliable measures of 5-HT(1A) binding. The large between-subject variability observed could not be explained by common methodological, physiological, or behavioral factors and hence the biological basis of this variability remains to be clarified.
正电子发射断层扫描(PET)对[(11)C]WAY-100635结合的研究正被证明是评估人体5-HT(1A)受体体内功能的一种有用工具。我们描述了[(11)C]WAY-100635在61名健康男性大脑中的结合模式,并研究了其变异性。对于所有PET扫描,使用简化参考组织模型(以小脑为参考区域)计算[(11)C]WAY-100635在不同区域的结合潜力(BP)值。具体而言,我们描述了(1)PET [(11)C]WAY-100635结合的感兴趣区域和统计参数映射(SPM)数据库,包括重测变异性;(2)[(11)C]WAY-100635结合对内源性5-HT操纵的敏感性;以及(3)[(11)C]WAY-100635结合与放射化学、人口统计学、生理学和行为变量之间的相关性。[(11)C]WAY-100635在健康人脑内的区域分布与体外报道的相似。重测变异性约为12%(范围9%-16%),并且对于所有区域采样方法而言相似。[(11)C]WAY-100635的结合对色氨酸输注和耗竭诱导的脑5-HT变化不敏感。尽管BP值在受试者之间差异很大(范围2.9-6.8),但区域和整体BP与常见的放射化学、人口统计学、生理学和人格变量之间没有显著相关性。具体而言,与最近两项小型研究相反,我们发现在我们年龄范围为24至53岁的大型队列中,[(11)C]WAY-100635结合没有随年龄下降。使用PET和[(11)C]WAY-100635对5-HT(1A)受体进行体内评估可得出5-HT(1A)结合的可靠测量值。观察到的受试者之间的巨大变异性无法用常见的方法学、生理学或行为因素来解释,因此这种变异性的生物学基础仍有待阐明。