@article{oai:repo.qst.go.jp:00046438,
 author = {Yamasaki, Tomoteru and Fujinaga, Masayuki and Kawamura, Kazunori and Yui, Joji and Hatori, Akiko and Ohya, Tomoyuki and Xie, Lin and Wakizaka, Hidekatsu and Yoshida, Yuichirou and Fukumura, Toshimitsu and Zhang, Ming-Rong and 山崎 友照 and 藤永 雅之 and 河村 和紀 and 由井 譲二 and 羽鳥 晶子 and 大矢 智幸 and 謝 琳 and 脇坂 秀克 and 吉田 勇一郎 and 福村 利光 and 張 明栄},
 issue = {10},
 journal = {Journal of Nuclear Medicine},
 month = {Aug},
 note = {Metabotropic glutamate receptor subtype 1 (mGluR1) is a crucial molecular target in the central nervous system disorders. 4-18F-fluoro-N-[4-[6-(isopropylamino)pyrimidin-4-yl]-1,3-thiazol-2-yl]-N-methylbenzamide (18F-FITM) has been recently developed as a useful PET ligand for mGluR1 imaging in our laboratory. In this study, we aimed to measure the affinity and density of mGluR1 using PET with 18F-FITM in rat brain under the in vivo conditions. Methods: Binding potentials (BPND) and amounts of specific binding (bound ligand concentration) at equilibrium state in brain regions were noninvasively estimated using the equilibrium analysis combined with the receptor-blocked approach (EA RBA) for kinetic analysis of 18F-FITM PET results in place of reference tissue methods. Using BPND and specific binding values of rats treated with multidose ligand, we performed Scatchard analyses for in vivo measurements of mGluR1 density (maximum number of binding sites, or Bmax) and ligand affinity (dissociation constant, or Kd) in brain regions, respectively. Results: The pretreatment of rats with unlabeled FITM (1 mg/kg) occupied an mGluR1 binding site of 18F-FITM by more than 99% and did not affect the input function. Hence, we used the tissue time–activity curve for receptor-blocked rats as representative of the nondisplaceable (free and nonspecific binding of radioligand) compartment. The BPND based on EA RBA showed a high correlation with the BPND based on invasive Logan plot graphical analysis in the thalamus, hippocampus, striatum, and cingulate cortex. The Kd (nM) and Bmax (pmol/mL) obtained by the Scatchard analyses with the multidose ligand assays were 2.1 and 36.3, respectively, for the thalamus; 2.1 and 27.5, respectively, for the hippocampus; 1.5 and 22.2, respectively, for the striatum; and 1.5 and 20.5, respectively, for the cingulate cortex with a high confidence. Conclusion: Our study is the first to our knowledge to measure the in vivo affinity (Kd and binding potential) of 18F-FITM and mGluR1 density (Bmax) with a high correlation to in vitro values in rat brain regions. This measurement using PET with 18F-FITM would be a useful index for research about mGluR1 functions in central nervous system disorders and development of new pharmaceuticals.},
 pages = {1601--1607},
 title = {In Vivo Measurement of the Affinity and Density of Metabotropic Glutamate Receptor Subtype 1 in Rat Brain Using 18F-FITM in Small-Animal PET},
 volume = {53},
 year = {2012}
}