Feasibility of deuterium magnetic resonance spectroscopy of 3-O-Methylglucose at 7 Tesla.

Deuterium Magnetic Resonance Spectroscopy (DMRS) is a non-invasive technique that allows the detection of deuterated compounds in vivo. DMRS has a large potential to analyze uptake, perfusion, washout or metabolism, since deuterium is a stable isotope and therefore does not decay during biologic pro...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Benedikt Hartmann, Max Müller, Lisa Seyler, Tobias Bäuerle, Tobias Wilferth, Nikolai Avdievitch, Loreen Ruhm, Anke Henning, Alexei Lesiv, Pavel Ivashkin, Michael Uder, Armin M Nagel
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/c4fbbe8fbc5a4bb0bdf2004e08926163
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:c4fbbe8fbc5a4bb0bdf2004e08926163
record_format dspace
spelling oai:doaj.org-article:c4fbbe8fbc5a4bb0bdf2004e089261632021-12-02T20:15:49ZFeasibility of deuterium magnetic resonance spectroscopy of 3-O-Methylglucose at 7 Tesla.1932-620310.1371/journal.pone.0252935https://doaj.org/article/c4fbbe8fbc5a4bb0bdf2004e089261632021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0252935https://doaj.org/toc/1932-6203Deuterium Magnetic Resonance Spectroscopy (DMRS) is a non-invasive technique that allows the detection of deuterated compounds in vivo. DMRS has a large potential to analyze uptake, perfusion, washout or metabolism, since deuterium is a stable isotope and therefore does not decay during biologic processing of a deuterium labelled substance. Moreover, DMRS allows the distinction between different deuterated substances. In this work, we performed DMRS of deuterated 3-O-Methylglucose (OMG). OMG is a non-metabolizable glucose analog which is transported similar to D-glucose. DMRS of OMG was performed in phantom and in vivo measurements using a preclinical 7 Tesla MRI system. The chemical shift (3.51 ± 0.1 ppm) and relaxation times were determined. OMG was injected intravenously and spectra were acquired over a period of one hour to monitor the time evolution of the deuterium signal in tumor-bearing rats. The increase and washout of OMG could be observed. Three different exponential functions were compared in terms of how well they describe the OMG washout. A mono-exponential model with offset seems to describe the observed time course best with a time constant of 1910 ± 770 s and an offset of 2.5 ± 1.2 mmol/l (mean ± std, N = 3). Chemical shift imaging could be performed with a voxel size of 7.1 mm x 7.1 mm x 7.9 mm. The feasibility of DMRS with deuterium labelled OMG could be demonstrated. These data might serve as basis for future studies that aim to characterize glucose transport using DMRS.Benedikt HartmannMax MüllerLisa SeylerTobias BäuerleTobias WilferthNikolai AvdievitchLoreen RuhmAnke HenningAlexei LesivPavel IvashkinMichael UderArmin M NagelPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 6, p e0252935 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Benedikt Hartmann
Max Müller
Lisa Seyler
Tobias Bäuerle
Tobias Wilferth
Nikolai Avdievitch
Loreen Ruhm
Anke Henning
Alexei Lesiv
Pavel Ivashkin
Michael Uder
Armin M Nagel
Feasibility of deuterium magnetic resonance spectroscopy of 3-O-Methylglucose at 7 Tesla.
description Deuterium Magnetic Resonance Spectroscopy (DMRS) is a non-invasive technique that allows the detection of deuterated compounds in vivo. DMRS has a large potential to analyze uptake, perfusion, washout or metabolism, since deuterium is a stable isotope and therefore does not decay during biologic processing of a deuterium labelled substance. Moreover, DMRS allows the distinction between different deuterated substances. In this work, we performed DMRS of deuterated 3-O-Methylglucose (OMG). OMG is a non-metabolizable glucose analog which is transported similar to D-glucose. DMRS of OMG was performed in phantom and in vivo measurements using a preclinical 7 Tesla MRI system. The chemical shift (3.51 ± 0.1 ppm) and relaxation times were determined. OMG was injected intravenously and spectra were acquired over a period of one hour to monitor the time evolution of the deuterium signal in tumor-bearing rats. The increase and washout of OMG could be observed. Three different exponential functions were compared in terms of how well they describe the OMG washout. A mono-exponential model with offset seems to describe the observed time course best with a time constant of 1910 ± 770 s and an offset of 2.5 ± 1.2 mmol/l (mean ± std, N = 3). Chemical shift imaging could be performed with a voxel size of 7.1 mm x 7.1 mm x 7.9 mm. The feasibility of DMRS with deuterium labelled OMG could be demonstrated. These data might serve as basis for future studies that aim to characterize glucose transport using DMRS.
format article
author Benedikt Hartmann
Max Müller
Lisa Seyler
Tobias Bäuerle
Tobias Wilferth
Nikolai Avdievitch
Loreen Ruhm
Anke Henning
Alexei Lesiv
Pavel Ivashkin
Michael Uder
Armin M Nagel
author_facet Benedikt Hartmann
Max Müller
Lisa Seyler
Tobias Bäuerle
Tobias Wilferth
Nikolai Avdievitch
Loreen Ruhm
Anke Henning
Alexei Lesiv
Pavel Ivashkin
Michael Uder
Armin M Nagel
author_sort Benedikt Hartmann
title Feasibility of deuterium magnetic resonance spectroscopy of 3-O-Methylglucose at 7 Tesla.
title_short Feasibility of deuterium magnetic resonance spectroscopy of 3-O-Methylglucose at 7 Tesla.
title_full Feasibility of deuterium magnetic resonance spectroscopy of 3-O-Methylglucose at 7 Tesla.
title_fullStr Feasibility of deuterium magnetic resonance spectroscopy of 3-O-Methylglucose at 7 Tesla.
title_full_unstemmed Feasibility of deuterium magnetic resonance spectroscopy of 3-O-Methylglucose at 7 Tesla.
title_sort feasibility of deuterium magnetic resonance spectroscopy of 3-o-methylglucose at 7 tesla.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/c4fbbe8fbc5a4bb0bdf2004e08926163
work_keys_str_mv AT benedikthartmann feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT maxmuller feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT lisaseyler feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT tobiasbauerle feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT tobiaswilferth feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT nikolaiavdievitch feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT loreenruhm feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT ankehenning feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT alexeilesiv feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT pavelivashkin feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT michaeluder feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
AT arminmnagel feasibilityofdeuteriummagneticresonancespectroscopyof3omethylglucoseat7tesla
_version_ 1718374550491627520