EJNMMI Research (Jul 2017)

Microglial depletion and activation: A [11C]PBR28 PET study in nonhuman primates

  • Ansel T. Hillmer,
  • Daniel Holden,
  • Krista Fowles,
  • Nabeel Nabulsi,
  • Brian L. West,
  • Richard E. Carson,
  • Kelly P. Cosgrove

DOI
https://doi.org/10.1186/s13550-017-0305-0
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 5

Abstract

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Abstract Background The 18-kDa translocator protein (TSPO) is an important target for assessing neuroimmune function in brain with positron-emission tomography (PET) imaging. The goal of this work was to assess two [11C]PBR28 imaging paradigms for measuring dynamic microglia changes in Macaca mulatta. Methods Dynamic [11C]PBR28 PET imaging data with arterial blood sampling were acquired to quantify TSPO levels as [11C]PBR28 V T. Scans were acquired at three timepoints: baseline, immediately post-drug, and prolonged post-drug. Results In one animal, a colony-stimulating factor 1 receptor kinase inhibitor, previously shown to deplete brain microglia, reduced [11C]PBR28 V T in brain by 46 ± 3% from baseline, which recovered after 12 days to 7 ± 5% from baseline. In a different animal, acute lipopolysaccharide administration, shown to activate brain microglia, increased [11C]PBR28 V T in brain by 39 ± 9% from baseline, which recovered after 14 days to −11 ± 3% from baseline. Conclusions These studies provide preliminary evidence of complementary paradigms to assess microglia dynamics via in vivo TSPO imaging.

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