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NMR shutter‐speed elucidates apparent population inversion of (1)H(2)O signals due to active transmembrane water cycling
PURPOSE: The desire to quantitatively discriminate the extra‐ and intracellular tissue (1)H(2)O MR signals has gone hand‐in‐hand with the continual, historic increase in MRI instrument magnetic field strength [B (0)]. However, recent studies have indicated extremely valuable, novel metabolic informa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593680/ https://www.ncbi.nlm.nih.gov/pubmed/30903632 http://dx.doi.org/10.1002/mrm.27725 |
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author | Li, Xin Mangia, Silvia Lee, Jing‐Huei Bai, Ruiliang Springer, Charles S. |
author_facet | Li, Xin Mangia, Silvia Lee, Jing‐Huei Bai, Ruiliang Springer, Charles S. |
author_sort | Li, Xin |
collection | PubMed |
description | PURPOSE: The desire to quantitatively discriminate the extra‐ and intracellular tissue (1)H(2)O MR signals has gone hand‐in‐hand with the continual, historic increase in MRI instrument magnetic field strength [B (0)]. However, recent studies have indicated extremely valuable, novel metabolic information can be readily accessible at ultra–low B (0). The two signals can be distinguished, and the homeostatic activity of the cell membrane sodium/potassium pump (Na(+),K(+),ATPase) detected. The mechanism allowing (1)H(2)O MRI to do this is the newly discovered active transmembrane water cycling (AWC) phenomenon, which we found using paramagnetic extracellular contrast agents at clinical B (0) values. AWC is important because Na(+),K(+),ATPase can be considered biology’s most vital enzyme, and its in vivo steady‐state activity has not before been measurable, let alone amenable to mapping with high spatial resolution. Recent reports indicate AWC correlates with neuronal firing rate, with malignant tumor metastatic potential, and inversely with cellular reducing equivalent fraction. We wish to systematize the ways AWC can be precisely measured. METHODS: We present a theoretical longitudinal relaxation analysis of considerable scope: it spans the low‐ and high–field situations. RESULTS: We show the NMR shutter‐speed organizing principle is pivotal in understanding how trans–membrane steady–state water exchange kinetics are manifest throughout the range. Our findings illuminate an aspect, apparent population inversion, which is crucial in understanding ultra‐low field results. CONCLUSIONS: Without an appreciation of apparent population inversion, significant misinterpretations of future data are likely. These could have unfortunate diagnostic consequences. |
format | Online Article Text |
id | pubmed-6593680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65936802019-07-10 NMR shutter‐speed elucidates apparent population inversion of (1)H(2)O signals due to active transmembrane water cycling Li, Xin Mangia, Silvia Lee, Jing‐Huei Bai, Ruiliang Springer, Charles S. Magn Reson Med Full Papers—Biophysics and Basic Biomedical Research PURPOSE: The desire to quantitatively discriminate the extra‐ and intracellular tissue (1)H(2)O MR signals has gone hand‐in‐hand with the continual, historic increase in MRI instrument magnetic field strength [B (0)]. However, recent studies have indicated extremely valuable, novel metabolic information can be readily accessible at ultra–low B (0). The two signals can be distinguished, and the homeostatic activity of the cell membrane sodium/potassium pump (Na(+),K(+),ATPase) detected. The mechanism allowing (1)H(2)O MRI to do this is the newly discovered active transmembrane water cycling (AWC) phenomenon, which we found using paramagnetic extracellular contrast agents at clinical B (0) values. AWC is important because Na(+),K(+),ATPase can be considered biology’s most vital enzyme, and its in vivo steady‐state activity has not before been measurable, let alone amenable to mapping with high spatial resolution. Recent reports indicate AWC correlates with neuronal firing rate, with malignant tumor metastatic potential, and inversely with cellular reducing equivalent fraction. We wish to systematize the ways AWC can be precisely measured. METHODS: We present a theoretical longitudinal relaxation analysis of considerable scope: it spans the low‐ and high–field situations. RESULTS: We show the NMR shutter‐speed organizing principle is pivotal in understanding how trans–membrane steady–state water exchange kinetics are manifest throughout the range. Our findings illuminate an aspect, apparent population inversion, which is crucial in understanding ultra‐low field results. CONCLUSIONS: Without an appreciation of apparent population inversion, significant misinterpretations of future data are likely. These could have unfortunate diagnostic consequences. John Wiley and Sons Inc. 2019-03-22 2019-07 /pmc/articles/PMC6593680/ /pubmed/30903632 http://dx.doi.org/10.1002/mrm.27725 Text en © 2019 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers—Biophysics and Basic Biomedical Research Li, Xin Mangia, Silvia Lee, Jing‐Huei Bai, Ruiliang Springer, Charles S. NMR shutter‐speed elucidates apparent population inversion of (1)H(2)O signals due to active transmembrane water cycling |
title | NMR shutter‐speed elucidates apparent population inversion of (1)H(2)O signals due to active transmembrane water cycling |
title_full | NMR shutter‐speed elucidates apparent population inversion of (1)H(2)O signals due to active transmembrane water cycling |
title_fullStr | NMR shutter‐speed elucidates apparent population inversion of (1)H(2)O signals due to active transmembrane water cycling |
title_full_unstemmed | NMR shutter‐speed elucidates apparent population inversion of (1)H(2)O signals due to active transmembrane water cycling |
title_short | NMR shutter‐speed elucidates apparent population inversion of (1)H(2)O signals due to active transmembrane water cycling |
title_sort | nmr shutter‐speed elucidates apparent population inversion of (1)h(2)o signals due to active transmembrane water cycling |
topic | Full Papers—Biophysics and Basic Biomedical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593680/ https://www.ncbi.nlm.nih.gov/pubmed/30903632 http://dx.doi.org/10.1002/mrm.27725 |
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