18F-ASEM, a radiolabeled antagonist for imaging the aα7-nicotinic acetylcholine receptor with PET

Andrew G. Horti, Yongjun Gao, Hiroto Kuwabara, Yuchuan Wang, Sofya Abazyan, Robert P. Yasuda, Thao Tran, Yingxian Xiao, Niaz Sahibzada, Daniel P. Holt, Kenneth J. Kellar, Mikhail V. Pletnikov, Martin G. Pomper, Dean F. Wong, Robert F. Dannals

Research output: Contribution to journalArticle

Abstract

The α7-nicotinic cholinergic receptor (α7-nAChR) is a key mediator of brain communication and has been implicated in a wide variety of central nervous system disorders. None of the currently available PET radioligands for α7-nAChR are suitable for quantitative PET imaging, mostly because of insufficient specific binding. The goal of this study was to evaluate the potential of 18F-ASEM (18F-JHU82132) as an α7-nAChR radioligand for PET. Methods: The inhibition binding assay and receptor functional properties of ASEM were assessed in vitro. The brain regional distribution of 18F-ASEM in baseline and blockade were evaluated in DISC1 mice (dissection) and baboons (PET). Results: ASEM is an antagonist for the α7-nAChR with high binding affinity (Ki 5 0.3 nM). 18F-ASEM readily entered the baboon brain and specifically labeled α7-nAChR. The in vivo specific binding of 18F-ASEM in the brain regions enriched with α7-nAChRs was 80%-90%. SSR180711, an α7-nAChR-selective partial agonist, blocked 18F-ASEM binding in the baboon brain in a dose-dependent manner, suggesting that the binding of 18F-ASEM was mediated by α7-nAChRs and the radioligand was suitable for drug evaluation studies. In the baboon baseline studies, the brain regional volume of distribution (VT) values for 18F-ASEM were 23 (thalamus), 22 (insula), 18 (hippocampus), and 14 (cerebellum), whereas in the binding selectivity (blockade) scan, all regional VT values were reduced to less than 4. The range of regional binding potential values in the baboon brain was from 3.9 to 6.6. In vivo cerebral binding of 18FASEM and α7-nAChR expression in mutant DISC1 mice, a rodent model of schizophrenia, was significantly lower than in control animals, which is in agreement with previous postmortem human data. Conclusion: 18F-ASEM holds promise as a radiotracer with suitable imaging properties for quantification of α7-nAChR in the human brain.

Original languageEnglish (US)
Pages (from-to)672-677
Number of pages6
JournalJournal of Nuclear Medicine
Volume55
Issue number4
DOIs
StatePublished - Apr 1 2014

Keywords

  • Baboon
  • Nicotine
  • PET
  • α7-nAChR

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

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