Development of Novel PET Probes for Central 2-Amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic Acid Receptors

被引:23
|
作者
Oi, Norihito [1 ,2 ]
Tokunaga, Masaki [2 ]
Suzuki, Michiyuki [1 ,2 ]
Nagai, Yuji [2 ]
Nakatani, Yosuke [1 ,2 ]
Yamamoto, Noboru [1 ]
Maeda, Jun [2 ]
Minamimoto, Takafumi [2 ]
Zhang, Ming-Rong [2 ]
Suhara, Tetsuya [2 ]
Higuchi, Makoto [2 ]
机构
[1] Eisai & Co Ltd, Tsukuba Res Labs, Tsukuba, Ibaraki 3002635, Japan
[2] Natl Inst Radiol Sci, Mol Imaging Ctr, Inage Ku, Chiba 2638555, Japan
关键词
POSITRON-EMISSION-TOMOGRAPHY; AMPA-RECEPTOR; GLUTAMATE RECEPTORS; ANTAGONIST; PERAMPANEL; OCCUPANCY; RADIOLIGANDS; DRUG; DISCOVERY; TARGETS;
D O I
10.1021/acs.jmedchem.5b00712
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We document the development of PET probes for central AMPA receptors and their application to in vivo animal imaging. An initial screening of perampanel derivatives was performed to identify probe candidates. Despite the high autoradiographic contrast yielded by several radioligands, rat PET scans did not support their in vivo suitability. Further focused derivatization and a second screening by ex vivo LC-MS measurements led to the selection of 2-[1-(3-methylaminophenyl)-2-oxo-5-(pyrimidin-2-yl)1,2-dihydropyridin-3-yl]benzonitrile, 21a, and its analogues as candidates. [C-11]21a was shown by autoradiography to specifically bind to the neocortex and hippocampus, consistent with AMPA receptor localization. PET imaging with [C-11]21a demonstrated moderate uptake of radioactivity in rat and monkey brains, with the retention of radiosignals being consistent with that from the autoradiogram data, and the uptake was blocked by pretreatment with unlabeled 21a in a dose-dependent manner. The current approach has facilitated the discovery of a PET probe potentially suitable for translational research and development focused on AMPA receptors.
引用
收藏
页码:8444 / 8462
页数:19
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