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

Purpose: In vivo ³¹P MRS magnetization transfer (MT) provides a direct measure of neuronal activity at the metabolic level. This work aims to use functional ³¹P MRS-MT to investigate the change in cerebral ATP metabolic rates in healthy adults upon repeated visual stimuli. Methods: A magnetizati...

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Main Authors: Chen, Chen, Stephenson, Mary C., Peters, Andrew, Morris, Peter G., Francis, Susan T., Gowland, Penny A.
Format: Article
Published: Wiley 2017
Subjects:
Online Access:https://eprints.nottingham.ac.uk/40872/
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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
building Nottingham Research Data Repository
collection Online Access
description Purpose: In vivo ³¹P MRS magnetization transfer (MT) provides a direct measure of neuronal activity at the metabolic level. This work aims to use functional ³¹P MRS-MT to investigate the change in cerebral 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 ³¹P MT experiments at 3 T. Results: Using progressive saturation of γ-ATP, the intrinsic T1 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, k₁, was observed upon visual stimulation in the first and second cycles respectively of a paradigm consisting of 10min-rest followed by 10min-stimulation, with the measured baseline k₁ being 0.35±0.04 s⁻¹. No significant changes in forward ATP synthase (ATPase) reaction rate, PCr/γ- ATP, Pi/γ-ATP, and NAD(H)/γ-ATP ratios, or intracellular pH were detected upon stimulation. Conclusion: This work demonstrates the potential of studying cerebral bioenergetics using functional ³¹P MRS-MT to determine the change in the forward CK reaction rate at 3 T.
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spelling nottingham-408722020-05-04T18:38:03Z https://eprints.nottingham.ac.uk/40872/ ³¹P 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. Purpose: In vivo ³¹P MRS magnetization transfer (MT) provides a direct measure of neuronal activity at the metabolic level. This work aims to use functional ³¹P MRS-MT to investigate the change in cerebral 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 ³¹P MT experiments at 3 T. Results: Using progressive saturation of γ-ATP, the intrinsic T1 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, k₁, was observed upon visual stimulation in the first and second cycles respectively of a paradigm consisting of 10min-rest followed by 10min-stimulation, with the measured baseline k₁ being 0.35±0.04 s⁻¹. No significant changes in forward ATP synthase (ATPase) reaction rate, PCr/γ- ATP, Pi/γ-ATP, and NAD(H)/γ-ATP ratios, or intracellular pH were detected upon stimulation. Conclusion: This work demonstrates the potential of studying cerebral bioenergetics using functional ³¹P MRS-MT to determine the change in the forward CK reaction rate at 3 T. Wiley 2017-03-16 Article PeerReviewed Chen, Chen, Stephenson, Mary C., Peters, Andrew, Morris, Peter G., Francis, Susan T. and Gowland, Penny A. (2017) ³¹P magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral ATP metabolic rates at 3 T. Magnetic Resonance in Medicine, 79 (1). pp. 22-30. ISSN 1522-2594 Adenosine triphosphate (ATP) metabolism; Magnetization transfer; In vivo 31P magnetic resonance spectroscopy (MRS); Visual stimulation; Bioenergetics; Brain http://onlinelibrary.wiley.com/doi/10.1002/mrm.26663/full doi:10.1002/mrm.26663 doi:10.1002/mrm.26663
spellingShingle Adenosine triphosphate (ATP) metabolism; Magnetization transfer; In vivo 31P magnetic resonance spectroscopy (MRS); Visual stimulation; Bioenergetics; Brain
Chen, Chen
Stephenson, Mary C.
Peters, Andrew
Morris, Peter G.
Francis, Susan T.
Gowland, Penny A.
³¹P magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title ³¹P magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_full ³¹P magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_fullStr ³¹P magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_full_unstemmed ³¹P magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_short ³¹P magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral ATP metabolic rates at 3 T
title_sort ³¹p magnetization transfer magnetic resonance spectroscopy: assessing the activation induced change in cerebral atp metabolic rates at 3 t
topic Adenosine triphosphate (ATP) metabolism; Magnetization transfer; In vivo 31P magnetic resonance spectroscopy (MRS); Visual stimulation; Bioenergetics; Brain
url https://eprints.nottingham.ac.uk/40872/
https://eprints.nottingham.ac.uk/40872/
https://eprints.nottingham.ac.uk/40872/