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Glucose exchange parameters in a subset of physiological conditions

The chemical exchange of labile protons of the hydroxyl groups can be exploited in a variety of magnetic resonance experiments to gain information about the groups and their physicochemical environment. The exchangeable –OH protons provide important contributions to the T(2) of water signals thus co...

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Autores principales: Mareš, J., Karjalainen, J., Håkansson, P., Michaeli, S., Liimatainen, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467565/
https://www.ncbi.nlm.nih.gov/pubmed/37593950
http://dx.doi.org/10.1039/d3cp01973j
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author Mareš, J.
Karjalainen, J.
Håkansson, P.
Michaeli, S.
Liimatainen, T.
author_facet Mareš, J.
Karjalainen, J.
Håkansson, P.
Michaeli, S.
Liimatainen, T.
author_sort Mareš, J.
collection PubMed
description The chemical exchange of labile protons of the hydroxyl groups can be exploited in a variety of magnetic resonance experiments to gain information about the groups and their physicochemical environment. The exchangeable –OH protons provide important contributions to the T(2) of water signals thus contributing to the T(2)-weighted contrast of MRI images. This exchange can be exploited more specifically and sensitively in chemical exchange saturation transfer (CEST) or longitudinal rotating frame relaxation (T(1,ρ)) experiments. Since glucose is omnipresent in living organisms, it may be seen as a rather universal probe. Even though the potential was first recognized many years ago, practical use has remained scarce due to numerous challenges. The major limitation is the rather low glucose concentration in most tissues. The other obstacles are related to multiple dependencies of the exchange parameters, such as temperature, pH, and concentration of various ions that are not known in sufficient detail for glucose. Thus, we embarked on evaluating the exchange parameters of a model that included every relevant chemical site for all –OH protons in both dominant enantiomers of glucose. We have (1) obtained conventional one-dimensional proton NMR spectra of glucose solutions in suitable temperature ranges, (2) we have iterated through several exchange models with various degrees of freedom determined by the number of distinguishable –OH proton sites and compared their performance, (3) we extrapolated the parameters of the best model of physiological temperature and (4) we demonstrated the use of the parameters in virtual experiments. As the main results, (1) we have obtained the temperature dependence of exchange parameters with reliable confidence intervals in three different pH values, with two of them reaching physiological temperature, and (2) we show how the parameters can be used in virtual experiments, helping to develop new applications for glucose as an NMR/MRI probe.
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spelling pubmed-104675652023-08-31 Glucose exchange parameters in a subset of physiological conditions Mareš, J. Karjalainen, J. Håkansson, P. Michaeli, S. Liimatainen, T. Phys Chem Chem Phys Chemistry The chemical exchange of labile protons of the hydroxyl groups can be exploited in a variety of magnetic resonance experiments to gain information about the groups and their physicochemical environment. The exchangeable –OH protons provide important contributions to the T(2) of water signals thus contributing to the T(2)-weighted contrast of MRI images. This exchange can be exploited more specifically and sensitively in chemical exchange saturation transfer (CEST) or longitudinal rotating frame relaxation (T(1,ρ)) experiments. Since glucose is omnipresent in living organisms, it may be seen as a rather universal probe. Even though the potential was first recognized many years ago, practical use has remained scarce due to numerous challenges. The major limitation is the rather low glucose concentration in most tissues. The other obstacles are related to multiple dependencies of the exchange parameters, such as temperature, pH, and concentration of various ions that are not known in sufficient detail for glucose. Thus, we embarked on evaluating the exchange parameters of a model that included every relevant chemical site for all –OH protons in both dominant enantiomers of glucose. We have (1) obtained conventional one-dimensional proton NMR spectra of glucose solutions in suitable temperature ranges, (2) we have iterated through several exchange models with various degrees of freedom determined by the number of distinguishable –OH proton sites and compared their performance, (3) we extrapolated the parameters of the best model of physiological temperature and (4) we demonstrated the use of the parameters in virtual experiments. As the main results, (1) we have obtained the temperature dependence of exchange parameters with reliable confidence intervals in three different pH values, with two of them reaching physiological temperature, and (2) we show how the parameters can be used in virtual experiments, helping to develop new applications for glucose as an NMR/MRI probe. The Royal Society of Chemistry 2023-08-01 /pmc/articles/PMC10467565/ /pubmed/37593950 http://dx.doi.org/10.1039/d3cp01973j Text en This journal is © the Owner Societies https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Mareš, J.
Karjalainen, J.
Håkansson, P.
Michaeli, S.
Liimatainen, T.
Glucose exchange parameters in a subset of physiological conditions
title Glucose exchange parameters in a subset of physiological conditions
title_full Glucose exchange parameters in a subset of physiological conditions
title_fullStr Glucose exchange parameters in a subset of physiological conditions
title_full_unstemmed Glucose exchange parameters in a subset of physiological conditions
title_short Glucose exchange parameters in a subset of physiological conditions
title_sort glucose exchange parameters in a subset of physiological conditions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467565/
https://www.ncbi.nlm.nih.gov/pubmed/37593950
http://dx.doi.org/10.1039/d3cp01973j
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AT liimatainent glucoseexchangeparametersinasubsetofphysiologicalconditions