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Positron Emission Tomography studies with [(11)C]PBR28 in the Healthy Rodent Brain: Validating SUV as an Outcome Measure of Neuroinflammation
Molecular imaging of the 18 kD Translocator protein (TSPO) with positron emission tomography (PET) is of great value for studying neuroinflammation in rodents longitudinally. Quantification of the TSPO in rodents is, however, quite challenging. There is no suitable reference region and the use of pl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440816/ https://www.ncbi.nlm.nih.gov/pubmed/25996996 http://dx.doi.org/10.1371/journal.pone.0125917 |
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author | Tóth, Miklós Doorduin, Janine Häggkvist, Jenny Varrone, Andrea Amini, Nahid Halldin, Christer Gulyás, Balázs |
author_facet | Tóth, Miklós Doorduin, Janine Häggkvist, Jenny Varrone, Andrea Amini, Nahid Halldin, Christer Gulyás, Balázs |
author_sort | Tóth, Miklós |
collection | PubMed |
description | Molecular imaging of the 18 kD Translocator protein (TSPO) with positron emission tomography (PET) is of great value for studying neuroinflammation in rodents longitudinally. Quantification of the TSPO in rodents is, however, quite challenging. There is no suitable reference region and the use of plasma-derived input is not an option for longitudinal studies. The aim of this study was therefore to evaluate the use of the standardized uptake value (SUV) as an outcome measure for TSPO imaging in rodent brain PET studies, using [(11)C]PBR28. In the first part of the study, healthy male Wistar rats (n = 4) were used to determine the correlation between the distribution volume (V(T), calculated with Logan graphical analysis) and the SUV. In the second part, healthy male Wistar rats (n = 4) and healthy male C57BL/6J mice (n = 4), were used to determine the test-retest variability of the SUV, with a 7-day interval between measurements. Dynamic PET scans of 63 minutes were acquired with a nanoScan PET/MRI and nanoScan PET/CT. An MRI scan was made for anatomical reference with each measurement. The whole brain V(T) of [(11)C]PBR28 in rats was 42.9 ± 1.7. A statistically significant correlation (r(2) = 0.96; p < 0.01) was found between the V(T) and the SUV. The test-retest variability in 8 brain region ranged from 8 to 20% in rats and from 7 to 23% in mice. The interclass correlation coefficient (ICC) was acceptable to excellent for rats, but poor to acceptable for mice. In conclusion: The SUV of [(11)C]PBR28 showed a high correlation with V(T) as well as good test-retest variability. For future longitudinal small animal PET studies the SUV can thus be used to describe [(11)C]PBR28 uptake in healthy brain tissue. Based on the present observations, further studies are needed to explore the applicability of this approach in small animal disease models, with special regard to neuroinflammatory models. |
format | Online Article Text |
id | pubmed-4440816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44408162015-05-29 Positron Emission Tomography studies with [(11)C]PBR28 in the Healthy Rodent Brain: Validating SUV as an Outcome Measure of Neuroinflammation Tóth, Miklós Doorduin, Janine Häggkvist, Jenny Varrone, Andrea Amini, Nahid Halldin, Christer Gulyás, Balázs PLoS One Research Article Molecular imaging of the 18 kD Translocator protein (TSPO) with positron emission tomography (PET) is of great value for studying neuroinflammation in rodents longitudinally. Quantification of the TSPO in rodents is, however, quite challenging. There is no suitable reference region and the use of plasma-derived input is not an option for longitudinal studies. The aim of this study was therefore to evaluate the use of the standardized uptake value (SUV) as an outcome measure for TSPO imaging in rodent brain PET studies, using [(11)C]PBR28. In the first part of the study, healthy male Wistar rats (n = 4) were used to determine the correlation between the distribution volume (V(T), calculated with Logan graphical analysis) and the SUV. In the second part, healthy male Wistar rats (n = 4) and healthy male C57BL/6J mice (n = 4), were used to determine the test-retest variability of the SUV, with a 7-day interval between measurements. Dynamic PET scans of 63 minutes were acquired with a nanoScan PET/MRI and nanoScan PET/CT. An MRI scan was made for anatomical reference with each measurement. The whole brain V(T) of [(11)C]PBR28 in rats was 42.9 ± 1.7. A statistically significant correlation (r(2) = 0.96; p < 0.01) was found between the V(T) and the SUV. The test-retest variability in 8 brain region ranged from 8 to 20% in rats and from 7 to 23% in mice. The interclass correlation coefficient (ICC) was acceptable to excellent for rats, but poor to acceptable for mice. In conclusion: The SUV of [(11)C]PBR28 showed a high correlation with V(T) as well as good test-retest variability. For future longitudinal small animal PET studies the SUV can thus be used to describe [(11)C]PBR28 uptake in healthy brain tissue. Based on the present observations, further studies are needed to explore the applicability of this approach in small animal disease models, with special regard to neuroinflammatory models. Public Library of Science 2015-05-21 /pmc/articles/PMC4440816/ /pubmed/25996996 http://dx.doi.org/10.1371/journal.pone.0125917 Text en © 2015 Tóth et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tóth, Miklós Doorduin, Janine Häggkvist, Jenny Varrone, Andrea Amini, Nahid Halldin, Christer Gulyás, Balázs Positron Emission Tomography studies with [(11)C]PBR28 in the Healthy Rodent Brain: Validating SUV as an Outcome Measure of Neuroinflammation |
title | Positron Emission Tomography studies with [(11)C]PBR28 in the Healthy Rodent Brain: Validating SUV as an Outcome Measure of Neuroinflammation |
title_full | Positron Emission Tomography studies with [(11)C]PBR28 in the Healthy Rodent Brain: Validating SUV as an Outcome Measure of Neuroinflammation |
title_fullStr | Positron Emission Tomography studies with [(11)C]PBR28 in the Healthy Rodent Brain: Validating SUV as an Outcome Measure of Neuroinflammation |
title_full_unstemmed | Positron Emission Tomography studies with [(11)C]PBR28 in the Healthy Rodent Brain: Validating SUV as an Outcome Measure of Neuroinflammation |
title_short | Positron Emission Tomography studies with [(11)C]PBR28 in the Healthy Rodent Brain: Validating SUV as an Outcome Measure of Neuroinflammation |
title_sort | positron emission tomography studies with [(11)c]pbr28 in the healthy rodent brain: validating suv as an outcome measure of neuroinflammation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440816/ https://www.ncbi.nlm.nih.gov/pubmed/25996996 http://dx.doi.org/10.1371/journal.pone.0125917 |
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