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(31)P magnetization transfer magnetic resonance spectroscopy: Assessing the activation induced change in cerebral ATP metabolic rates at 3 T

PURPOSE: In vivo (31)P magnetic resonance spectroscopy (MRS) magnetization transfer (MT) provides a direct measure of neuronal activity at the metabolic level. This work aims to use functional (31)P MRS‐MT to investigate the change in cerebral adenosine triphosphate (ATP) metabolic rates in healthy...

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Autores principales: Chen, Chen, Stephenson, Mary C., Peters, Andrew, Morris, Peter G., Francis, Susan T., Gowland, Penny A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706641/
https://www.ncbi.nlm.nih.gov/pubmed/28303591
http://dx.doi.org/10.1002/mrm.26663
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author Chen, Chen
Stephenson, Mary C.
Peters, Andrew
Morris, Peter G.
Francis, Susan T.
Gowland, Penny A.
author_facet Chen, Chen
Stephenson, Mary C.
Peters, Andrew
Morris, Peter G.
Francis, Susan T.
Gowland, Penny A.
author_sort Chen, Chen
collection PubMed
description PURPOSE: In vivo (31)P magnetic resonance spectroscopy (MRS) magnetization transfer (MT) provides a direct measure of neuronal activity at the metabolic level. This work aims to use functional (31)P MRS‐MT to investigate the change in cerebral adenosine triphosphate (ATP) metabolic rates in healthy adults upon repeated visual stimuli. METHODS: A magnetization saturation transfer sequence with narrowband selective saturation of γ‐ATP was developed for (31)P MT experiments at 3 T. RESULTS: Using progressive saturation of γ‐ATP, the intrinsic T(1) relaxation times of phosphocreatine (PCr) and inorganic phosphate (Pi) at 3 T were measured to be 5.1 ± 0.8 s and 3.0 ± 1.4 s, respectively. Using steady‐state saturation of γ‐ATP, a significant 24% ± 14% and 11% ± 7% increase in the forward creatine kinase (CK) pseudo‐first‐order reaction rate constant, k (1), was observed upon visual stimulation in the first and second cycles, respectively, of a paradigm consisting of 10‐minute rest followed by 10‐minute stimulation, with the measured baseline k (1) being 0.35 ± 0.04 s(−1). No significant changes in forward ATP synthase reaction rate, PCr/γ‐ATP, Pi/γ‐ATP, and nicotinamide adenine dinucleotide/γ‐ATP ratios, or intracellular pH were detected upon stimulation. CONCLUSION: This work demonstrates the potential of studying cerebral bioenergetics using functional (31)P MRS‐MT to determine the change in the forward CK reaction rate at 3 T. Magn Reson Med 79:22–30, 2018. © 2017 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 Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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spelling pubmed-57066412018-01-01 (31)P magnetization transfer magnetic resonance spectroscopy: Assessing the activation induced change in cerebral ATP metabolic rates at 3 T Chen, Chen Stephenson, Mary C. Peters, Andrew Morris, Peter G. Francis, Susan T. Gowland, Penny A. Magn Reson Med Full Papers—Spectroscopic Methodology PURPOSE: In vivo (31)P magnetic resonance spectroscopy (MRS) magnetization transfer (MT) provides a direct measure of neuronal activity at the metabolic level. This work aims to use functional (31)P MRS‐MT to investigate the change in cerebral adenosine triphosphate (ATP) metabolic rates in healthy adults upon repeated visual stimuli. METHODS: A magnetization saturation transfer sequence with narrowband selective saturation of γ‐ATP was developed for (31)P MT experiments at 3 T. RESULTS: Using progressive saturation of γ‐ATP, the intrinsic T(1) relaxation times of phosphocreatine (PCr) and inorganic phosphate (Pi) at 3 T were measured to be 5.1 ± 0.8 s and 3.0 ± 1.4 s, respectively. Using steady‐state saturation of γ‐ATP, a significant 24% ± 14% and 11% ± 7% increase in the forward creatine kinase (CK) pseudo‐first‐order reaction rate constant, k (1), was observed upon visual stimulation in the first and second cycles, respectively, of a paradigm consisting of 10‐minute rest followed by 10‐minute stimulation, with the measured baseline k (1) being 0.35 ± 0.04 s(−1). No significant changes in forward ATP synthase reaction rate, PCr/γ‐ATP, Pi/γ‐ATP, and nicotinamide adenine dinucleotide/γ‐ATP ratios, or intracellular pH were detected upon stimulation. CONCLUSION: This work demonstrates the potential of studying cerebral bioenergetics using functional (31)P MRS‐MT to determine the change in the forward CK reaction rate at 3 T. Magn Reson Med 79:22–30, 2018. © 2017 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 Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. John Wiley and Sons Inc. 2017-03-16 2018-01 /pmc/articles/PMC5706641/ /pubmed/28303591 http://dx.doi.org/10.1002/mrm.26663 Text en © 2017 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers—Spectroscopic Methodology
Chen, Chen
Stephenson, Mary C.
Peters, Andrew
Morris, Peter G.
Francis, Susan T.
Gowland, Penny A.
(31)P magnetization transfer magnetic resonance spectroscopy: Assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title (31)P magnetization transfer magnetic resonance spectroscopy: Assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_full (31)P magnetization transfer magnetic resonance spectroscopy: Assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_fullStr (31)P magnetization transfer magnetic resonance spectroscopy: Assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_full_unstemmed (31)P magnetization transfer magnetic resonance spectroscopy: Assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_short (31)P magnetization transfer magnetic resonance spectroscopy: Assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_sort (31)p magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral atp metabolic rates at 3 t
topic Full Papers—Spectroscopic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706641/
https://www.ncbi.nlm.nih.gov/pubmed/28303591
http://dx.doi.org/10.1002/mrm.26663
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