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Comparison of four (11)C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176—based on recent publications that measured specific-to-non-displaceable ratios

Translocator protein (TSPO) is a biomarker for detecting neuroinflammation by PET. (11)C-(R)-PK11195 has been used to image TSPO since the 1980s. Here, we compared the utility of four (11)C-labeled ligands—(R)-PK11195, PBR28, DPA-713, and ER176—to quantify TSPO in healthy humans. For all of these li...

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Autores principales: Fujita, Masahiro, Kobayashi, Masato, Ikawa, Masamichi, Gunn, Roger N., Rabiner, Eugenii A., Owen, David R., Zoghbi, Sami S., Haskali, Mohamad B., Telu, Sanjay, Pike, Victor W., Innis, Robert B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643834/
https://www.ncbi.nlm.nih.gov/pubmed/29038960
http://dx.doi.org/10.1186/s13550-017-0334-8
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author Fujita, Masahiro
Kobayashi, Masato
Ikawa, Masamichi
Gunn, Roger N.
Rabiner, Eugenii A.
Owen, David R.
Zoghbi, Sami S.
Haskali, Mohamad B.
Telu, Sanjay
Pike, Victor W.
Innis, Robert B.
author_facet Fujita, Masahiro
Kobayashi, Masato
Ikawa, Masamichi
Gunn, Roger N.
Rabiner, Eugenii A.
Owen, David R.
Zoghbi, Sami S.
Haskali, Mohamad B.
Telu, Sanjay
Pike, Victor W.
Innis, Robert B.
author_sort Fujita, Masahiro
collection PubMed
description Translocator protein (TSPO) is a biomarker for detecting neuroinflammation by PET. (11)C-(R)-PK11195 has been used to image TSPO since the 1980s. Here, we compared the utility of four (11)C-labeled ligands—(R)-PK11195, PBR28, DPA-713, and ER176—to quantify TSPO in healthy humans. For all of these ligands, BP (ND) (specific-to-non-displaceable ratio of distribution volumes) was measured by partially blocking specific binding with XNBD173 administration. In high-affinity binders, DPA-713 showed the highest BP (ND) of 7.3 followed by ER176 (4.2), PBR28 (1.2), and PK11195 (0.8). Only ER176 allows the inclusion of low-affinity binders because of little influence of radiometabolites and high BP (ND). If inclusion of all three genotypes is important for study logistics, ER176 is the best of these four radioligands for studying neuroinflammation.
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spelling pubmed-56438342017-11-07 Comparison of four (11)C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176—based on recent publications that measured specific-to-non-displaceable ratios Fujita, Masahiro Kobayashi, Masato Ikawa, Masamichi Gunn, Roger N. Rabiner, Eugenii A. Owen, David R. Zoghbi, Sami S. Haskali, Mohamad B. Telu, Sanjay Pike, Victor W. Innis, Robert B. EJNMMI Res Commentary Translocator protein (TSPO) is a biomarker for detecting neuroinflammation by PET. (11)C-(R)-PK11195 has been used to image TSPO since the 1980s. Here, we compared the utility of four (11)C-labeled ligands—(R)-PK11195, PBR28, DPA-713, and ER176—to quantify TSPO in healthy humans. For all of these ligands, BP (ND) (specific-to-non-displaceable ratio of distribution volumes) was measured by partially blocking specific binding with XNBD173 administration. In high-affinity binders, DPA-713 showed the highest BP (ND) of 7.3 followed by ER176 (4.2), PBR28 (1.2), and PK11195 (0.8). Only ER176 allows the inclusion of low-affinity binders because of little influence of radiometabolites and high BP (ND). If inclusion of all three genotypes is important for study logistics, ER176 is the best of these four radioligands for studying neuroinflammation. Springer Berlin Heidelberg 2017-10-16 /pmc/articles/PMC5643834/ /pubmed/29038960 http://dx.doi.org/10.1186/s13550-017-0334-8 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 Commentary
Fujita, Masahiro
Kobayashi, Masato
Ikawa, Masamichi
Gunn, Roger N.
Rabiner, Eugenii A.
Owen, David R.
Zoghbi, Sami S.
Haskali, Mohamad B.
Telu, Sanjay
Pike, Victor W.
Innis, Robert B.
Comparison of four (11)C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176—based on recent publications that measured specific-to-non-displaceable ratios
title Comparison of four (11)C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176—based on recent publications that measured specific-to-non-displaceable ratios
title_full Comparison of four (11)C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176—based on recent publications that measured specific-to-non-displaceable ratios
title_fullStr Comparison of four (11)C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176—based on recent publications that measured specific-to-non-displaceable ratios
title_full_unstemmed Comparison of four (11)C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176—based on recent publications that measured specific-to-non-displaceable ratios
title_short Comparison of four (11)C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176—based on recent publications that measured specific-to-non-displaceable ratios
title_sort comparison of four (11)c-labeled pet ligands to quantify translocator protein 18 kda (tspo) in human brain: (r)-pk11195, pbr28, dpa-713, and er176—based on recent publications that measured specific-to-non-displaceable ratios
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643834/
https://www.ncbi.nlm.nih.gov/pubmed/29038960
http://dx.doi.org/10.1186/s13550-017-0334-8
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