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Evaluation of two potent and selective PET radioligands to image COX-1 and COX-2 in rhesus monkeys

  • Min Jeong Kim
  • , Stal S. Shrestha
  • , Michelle Cortes
  • , Prachi Singh
  • , Cheryl Morse
  • , Jeih San Liow
  • , Robert L. Gladding
  • , Chad Brouwer
  • , Katharine Henry
  • , Evan Gallagher
  • , George L. Tye
  • , Sami S. Zoghbi
  • , Masahiro Fujita
  • , Victor W. Pike
  • , Robert B. Innis
  • National Institutes of Health

Research output: Contribution to journalArticlepeer-review

49 Scopus citations

Abstract

This study assessed whether the newly developed PET radioligands11C-PS13 and11C-MC1 could image constitutive levels of cyclooxygenase (COX)-1 and COX-2, respectively, in rhesus monkeys. Methods: After intravenous injection of either radioligand, 24 whole-body PET scans were performed. To measure enzyme-specific uptake, scans of the 2 radioligands were also performed after administration of a nonradioactive drug preferential for either COX-1 or COX-2. Concurrent venous samples were obtained to measure parent radioligand concentrations. SUVs were calculated from 10 to 90 min. Results:11C-PS13 showed specific uptake in most organs, including spleen, gastrointestinal tract, kidneys, and brain, which was blocked by COX-1, but not COX-2, preferential inhibitors. Specific uptake of11C-MC1 was not observed in any organ except the ovaries and possibly kidneys. Conclusion: The findings suggest that11C-PS13 has adequate signal in monkeys to justify its extension to human subjects. In contrast,11C-MC1 is unlikely to show significant signal in healthy humans, though it may be able to do so in inflammatory conditions.

Original languageEnglish
Pages (from-to)1907-1912
Number of pages6
JournalJournal of Nuclear Medicine
Volume59
Issue number12
DOIs
StatePublished - Dec 1 2018

Keywords

  • Cyclooxygenase-1
  • Cyclooxygenase-2
  • Inflammation
  • Nonsteroidal antiinflammatory agents
  • Positron-emission tomography

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