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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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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. |
format | Online Article Text |
id | pubmed-5524658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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