Feasibility of in vivo measurement of glucose metabolism in the mouse hypothalamus by 1 H-[13 C] MRS at 14.1T
Lizarbe, Blanca ; Lei, Hongxia ; Duarte, Joao M N LU
; Lanz, Bernard
; Cherix, Antoine
and Gruetter, Rolf
(2018)
In Magnetic Resonance in Medicine
80(3).
p.874-884
- Abstract
PURPOSE: Determine the feasibility of 1 H-[13 C] MRS in the mouse hypothalamus using a 14.1T magnet.
METHODS: We optimized the design of a 1 H-[13 C] surface coil to maximize the signal-to-noise ratio of 1 H-[13 C] MRS in the mouse hypothalamus. With enhanced signal, 13 C accumulation in glucose metabolites was measured in a 8.7 µL voxel in the hypothalamus of 5 healthy mice during the continuous administration of [1,6-13 C2 ]glucose.
RESULTS: Accumulation of 13 C label in glucose C6 and lactate C3 was visible in the hypothalamus 11 min after glucose administration. The 13 C fractional enrichment (FE) curves of lactate C3, glutamate and glutamine C4, glutamate+glutamine C3 and C2, GABA C2, C3, and C4, and aspartate C3 were... (More)
PURPOSE: Determine the feasibility of 1 H-[13 C] MRS in the mouse hypothalamus using a 14.1T magnet.
METHODS: We optimized the design of a 1 H-[13 C] surface coil to maximize the signal-to-noise ratio of 1 H-[13 C] MRS in the mouse hypothalamus. With enhanced signal, 13 C accumulation in glucose metabolites was measured in a 8.7 µL voxel in the hypothalamus of 5 healthy mice during the continuous administration of [1,6-13 C2 ]glucose.
RESULTS: Accumulation of 13 C label in glucose C6 and lactate C3 was visible in the hypothalamus 11 min after glucose administration. The 13 C fractional enrichment (FE) curves of lactate C3, glutamate and glutamine C4, glutamate+glutamine C3 and C2, GABA C2, C3, and C4, and aspartate C3 were measured with a time resolution of 11 min over 190 min. FE time-courses and metabolic pool sizes were averaged to fit a novel one-compartment model of brain energy metabolism that incorporates the main features of the hypothalamus.
CONCLUSION: Dynamic 1 H-[13 C] MRS is able to measure in vivo brain metabolism in small and deep areas of the mouse brain such as the hypothalamus, and it can be used to calculate metabolic fluxes, including glutamatergic and GABAergic metabolism as well as the contribution of metabolic sources other than glucose.
(Less)
- author
- Lizarbe, Blanca
; Lei, Hongxia
; Duarte, Joao M N
LU
; Lanz, Bernard
; Cherix, Antoine
and Gruetter, Rolf
- publishing date
- 2018-09
- type
- Contribution to journal
- publication status
- published
- in
- Magnetic Resonance in Medicine
- volume
- 80
- issue
- 3
- pages
- 874 - 884
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- pmid:29427382
- scopus:85041523201
- ISSN
- 1522-2594
- DOI
- 10.1002/mrm.27129
- language
- English
- LU publication?
- no
- id
- 02ab9ea8-0247-48fe-8921-4fa1fc8de36c
- date added to LUP
- 2019-02-22 09:13:31
- date last changed
- 2024-06-11 05:27:30
@article{02ab9ea8-0247-48fe-8921-4fa1fc8de36c,
abstract = {{<p>PURPOSE: Determine the feasibility of 1 H-[13 C] MRS in the mouse hypothalamus using a 14.1T magnet.</p><p>METHODS: We optimized the design of a 1 H-[13 C] surface coil to maximize the signal-to-noise ratio of 1 H-[13 C] MRS in the mouse hypothalamus. With enhanced signal, 13 C accumulation in glucose metabolites was measured in a 8.7 µL voxel in the hypothalamus of 5 healthy mice during the continuous administration of [1,6-13 C2 ]glucose.</p><p>RESULTS: Accumulation of 13 C label in glucose C6 and lactate C3 was visible in the hypothalamus 11 min after glucose administration. The 13 C fractional enrichment (FE) curves of lactate C3, glutamate and glutamine C4, glutamate+glutamine C3 and C2, GABA C2, C3, and C4, and aspartate C3 were measured with a time resolution of 11 min over 190 min. FE time-courses and metabolic pool sizes were averaged to fit a novel one-compartment model of brain energy metabolism that incorporates the main features of the hypothalamus.</p><p>CONCLUSION: Dynamic 1 H-[13 C] MRS is able to measure in vivo brain metabolism in small and deep areas of the mouse brain such as the hypothalamus, and it can be used to calculate metabolic fluxes, including glutamatergic and GABAergic metabolism as well as the contribution of metabolic sources other than glucose.</p>}},
author = {{Lizarbe, Blanca and Lei, Hongxia and Duarte, Joao M N and Lanz, Bernard and Cherix, Antoine and Gruetter, Rolf}},
issn = {{1522-2594}},
language = {{eng}},
number = {{3}},
pages = {{874--884}},
publisher = {{John Wiley & Sons Inc.}},
series = {{Magnetic Resonance in Medicine}},
title = {{Feasibility of in vivo measurement of glucose metabolism in the mouse hypothalamus by 1 H-[13 C] MRS at 14.1T}},
url = {{http://dx.doi.org/10.1002/mrm.27129}},
doi = {{10.1002/mrm.27129}},
volume = {{80}},
year = {{2018}},
}