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The z-spectrum from human blood at 7T
Chemical Exchange Saturation Transfer (CEST) has been used to assess healthy and pathological tissue in both animals and humans. However, the CEST signal from blood has not been fully assessed. This paper presents the CEST and nuclear Overhauser enhancement (NOE) signals detected in human blood meas...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854271/ https://www.ncbi.nlm.nih.gov/pubmed/29111410 http://dx.doi.org/10.1016/j.neuroimage.2017.10.053 |
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author | Shah, Simon M. Mougin, Olivier E. Carradus, Andrew J. Geades, Nicolas Dury, Richard Morley, William Gowland, Penny A. |
author_facet | Shah, Simon M. Mougin, Olivier E. Carradus, Andrew J. Geades, Nicolas Dury, Richard Morley, William Gowland, Penny A. |
author_sort | Shah, Simon M. |
collection | PubMed |
description | Chemical Exchange Saturation Transfer (CEST) has been used to assess healthy and pathological tissue in both animals and humans. However, the CEST signal from blood has not been fully assessed. This paper presents the CEST and nuclear Overhauser enhancement (NOE) signals detected in human blood measured via z-spectrum analysis. We assessed the effects of blood oxygenation levels, haematocrit, cell structure and pH upon the z-spectrum in ex vivo human blood for different saturation powers at 7T. The data were analysed using Lorentzian difference (LD) model fitting and AREX (to compensate for changes in T(1)), which have been successfully used to study CEST effects in vivo. Full Bloch-McConnell fitting was also performed to provide an initial estimate of exchange rates and transverse relaxation rates of the various pools. CEST and NOE signals were observed at 3.5 ppm, −1.7 ppm and −3.5 ppm and were found to originate primarily from the red blood cells (RBCs), although the amide proton transfer (APT) CEST effect, and NOEs showed no dependence upon oxygenation levels. Upon lysing, the APT and NOE signals fell significantly. Different pH levels in blood resulted in changes in both the APT and NOE (at −3.5 ppm), which suggests that this NOE signal is in part an exchange relayed process. These results will be important for assessing in vivo z-spectra. |
format | Online Article Text |
id | pubmed-5854271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58542712018-03-16 The z-spectrum from human blood at 7T Shah, Simon M. Mougin, Olivier E. Carradus, Andrew J. Geades, Nicolas Dury, Richard Morley, William Gowland, Penny A. Neuroimage Article Chemical Exchange Saturation Transfer (CEST) has been used to assess healthy and pathological tissue in both animals and humans. However, the CEST signal from blood has not been fully assessed. This paper presents the CEST and nuclear Overhauser enhancement (NOE) signals detected in human blood measured via z-spectrum analysis. We assessed the effects of blood oxygenation levels, haematocrit, cell structure and pH upon the z-spectrum in ex vivo human blood for different saturation powers at 7T. The data were analysed using Lorentzian difference (LD) model fitting and AREX (to compensate for changes in T(1)), which have been successfully used to study CEST effects in vivo. Full Bloch-McConnell fitting was also performed to provide an initial estimate of exchange rates and transverse relaxation rates of the various pools. CEST and NOE signals were observed at 3.5 ppm, −1.7 ppm and −3.5 ppm and were found to originate primarily from the red blood cells (RBCs), although the amide proton transfer (APT) CEST effect, and NOEs showed no dependence upon oxygenation levels. Upon lysing, the APT and NOE signals fell significantly. Different pH levels in blood resulted in changes in both the APT and NOE (at −3.5 ppm), which suggests that this NOE signal is in part an exchange relayed process. These results will be important for assessing in vivo z-spectra. Academic Press 2018-02-15 /pmc/articles/PMC5854271/ /pubmed/29111410 http://dx.doi.org/10.1016/j.neuroimage.2017.10.053 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shah, Simon M. Mougin, Olivier E. Carradus, Andrew J. Geades, Nicolas Dury, Richard Morley, William Gowland, Penny A. The z-spectrum from human blood at 7T |
title | The z-spectrum from human blood at 7T |
title_full | The z-spectrum from human blood at 7T |
title_fullStr | The z-spectrum from human blood at 7T |
title_full_unstemmed | The z-spectrum from human blood at 7T |
title_short | The z-spectrum from human blood at 7T |
title_sort | z-spectrum from human blood at 7t |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854271/ https://www.ncbi.nlm.nih.gov/pubmed/29111410 http://dx.doi.org/10.1016/j.neuroimage.2017.10.053 |
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