PT  - JOURNAL ARTICLE
AU  - Shrestha, Stal S.
AU  - Liow, Jeih-San
AU  - Jenko, Kimberly
AU  - Ikawa, Masamichi
AU  - Zoghbi, Sami S.
AU  - Innis, Robert B.
TI  - The 5-HT<sub>1A</sub> Receptor PET Radioligand <sup>11</sup>C-CUMI-101 Has Significant Binding to α<sub>1</sub>-Adrenoceptors in Human Cerebellum, Limiting Its Use as a Reference Region
AID  - 10.2967/jnumed.116.174151
DP  - 2016 Dec 01
TA  - Journal of Nuclear Medicine
PG  - 1945--1948
VI  - 57
IP  - 12
4099  - http://jnm.snmjournals.org/content/57/12/1945.short
4100  - http://jnm.snmjournals.org/content/57/12/1945.full
SO  - J Nucl Med2016 Dec 01; 57
AB  - Prazosin, a potent and selective α1-adrenoceptor antagonist, displaces 25% of 11C-CUMI-101 ([O-methyl-11C]2-(4-(4-(2-methoxyphenyl)piperazin-1-yl)butyl)-4-methyl-1,2,4-triazine-3,5(2H,4H)dione) binding in monkey cerebellum. We sought to estimate the percentage contamination of 11C-CUMI-101 binding to α1-adrenoceptors in human cerebellum under in vivo conditions. In vitro receptor-binding techniques were used to measure α1-adrenoceptor density and the affinity of CUMI-101 for these receptors in human, monkey, and rat cerebellum. Methods: Binding potential (maximum number of binding sites × affinity [(1/dissociation constant]) was determined using in vitro homogenate binding assays in human, monkey, and rat cerebellum. 3H-prazosin was used to determine the maximum number of binding sites, as well as the dissociation constant of 3H-prazosin and the inhibition constant of CUMI-101. Results: α1-adrenoceptor density and the affinity of CUMI-101 for these receptors were similar across species. Cerebellar binding potentials were 3.7 for humans, 2.3 for monkeys, and 3.4 for rats. Conclusion: Reasoning by analogy, 25% of 11C-CUMI-101 uptake in human cerebellum reflects binding to α1-adrenoceptors, suggesting that the cerebellum is of limited usefulness as a reference tissue for quantification in human studies.