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

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 [(11)C]PBR28 imaging paradigms for measuring dynamic microglia changes in Macaca mulatta. MET...

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Autores principales: Hillmer, Ansel T., Holden, Daniel, Fowles, Krista, Nabulsi, Nabeel, West, Brian L., Carson, Richard E., Cosgrove, Kelly P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524658/
https://www.ncbi.nlm.nih.gov/pubmed/28741281
http://dx.doi.org/10.1186/s13550-017-0305-0
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author Hillmer, Ansel T.
Holden, Daniel
Fowles, Krista
Nabulsi, Nabeel
West, Brian L.
Carson, Richard E.
Cosgrove, Kelly P.
author_facet Hillmer, Ansel T.
Holden, Daniel
Fowles, Krista
Nabulsi, Nabeel
West, Brian L.
Carson, Richard E.
Cosgrove, Kelly P.
author_sort Hillmer, Ansel T.
collection PubMed
description 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 [(11)C]PBR28 imaging paradigms for measuring dynamic microglia changes in Macaca mulatta. METHODS: Dynamic [(11)C]PBR28 PET imaging data with arterial blood sampling were acquired to quantify TSPO levels as [(11)C]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 [(11)C]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 [(11)C]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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spelling pubmed-55246582017-08-08 Microglial depletion and activation: A [(11)C]PBR28 PET study in nonhuman primates Hillmer, Ansel T. Holden, Daniel Fowles, Krista Nabulsi, Nabeel West, Brian L. Carson, Richard E. Cosgrove, Kelly P. EJNMMI Res Preliminary Research 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 [(11)C]PBR28 imaging paradigms for measuring dynamic microglia changes in Macaca mulatta. METHODS: Dynamic [(11)C]PBR28 PET imaging data with arterial blood sampling were acquired to quantify TSPO levels as [(11)C]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 [(11)C]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 [(11)C]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. Springer Berlin Heidelberg 2017-07-24 /pmc/articles/PMC5524658/ /pubmed/28741281 http://dx.doi.org/10.1186/s13550-017-0305-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Preliminary Research
Hillmer, Ansel T.
Holden, Daniel
Fowles, Krista
Nabulsi, Nabeel
West, Brian L.
Carson, Richard E.
Cosgrove, Kelly P.
Microglial depletion and activation: A [(11)C]PBR28 PET study in nonhuman primates
title Microglial depletion and activation: A [(11)C]PBR28 PET study in nonhuman primates
title_full Microglial depletion and activation: A [(11)C]PBR28 PET study in nonhuman primates
title_fullStr Microglial depletion and activation: A [(11)C]PBR28 PET study in nonhuman primates
title_full_unstemmed Microglial depletion and activation: A [(11)C]PBR28 PET study in nonhuman primates
title_short Microglial depletion and activation: A [(11)C]PBR28 PET study in nonhuman primates
title_sort microglial depletion and activation: a [(11)c]pbr28 pet study in nonhuman primates
topic Preliminary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524658/
https://www.ncbi.nlm.nih.gov/pubmed/28741281
http://dx.doi.org/10.1186/s13550-017-0305-0
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