In vivo γ-aminobutyric acid measurement in rats with spectral editing at 4.7T
View / Open Files
Authors
Jupp, Bianca
Taylor, Tom
Caprioli, Daniele
Publication Date
2015-12-03Journal Title
Journal of Magnetic Resonance Imaging
ISSN
1053-1807
Publisher
Wiley
Language
English
Type
Article
Metadata
Show full item recordCitation
Sawiak, S., Jupp, B., Taylor, T., Caprioli, D., Carpenter, A., & Dalley, J. (2015). In vivo γ-aminobutyric acid measurement in rats with spectral editing at 4.7T. Journal of Magnetic Resonance Imaging https://doi.org/10.1002/jmri.25093
Abstract
Purpose
To evaluate the feasibility of spectral editing for quantification of γ-aminobutyric acid (GABA) in the rat brain and to determine whether altered GABA concentration in the ventral striatum is a neural endophenotype associated with trait-like impulsive behavior.
Materials and Methods
Spectra were acquired at 4.7T for 23 male Lister-hooded rats that had been previously screened for extremely low and high impulsivity phenotypes on an automated behavioral task (n = 11 low-impulsive; n = 12 high-impulsive). Voxels of 3 × 7 × 4 mm3 (84 μL) centered bilaterally across the ventral striatum were used to evaluate GABA concentration ratios.
Results
Quantifiable GABA signals in the ventral striatum were obtained for all rats. Mean-edited GABA to n-acetyl aspartate (NAA) ratios in the ventral striatum were 0.22 (95% confidence interval [CI] [0.18, 0.25]). Mean GABA/NAA ratios in this region were significantly decreased by 28% in high-impulsive rats compared to low-impulsive rats (P = 0.02; 95% CI [–53%, –2%]).
Conclusion
These findings demonstrate that spectral editing at 4.7T is a feasible method to assess in vivo GABA concentrations in the rat brain. The results show that diminished GABA content in the ventral striatum may be a neural endophenotype associated with impulsivity. J. Magn. Reson. Imaging 2015.
Keywords
spectroscopy, behavior, nucleus accumbens, striatum, GABA
Sponsorship
This study was funded by the UK Medical Research Council (G0701500) and by a joint award from the Medical Research Council (G1000183) and Wellcome Trust (093875/Z/10/Z) in support of the Behavioural and Clinical Neuroscience Institute at Cambridge University. BJ is supported by grants from the AXA Research Fund and the Australian National Health and Medical Research Council (1016313).
Funder references
MEDICAL RESEARCH COUNCIL (G0001354)
MRC (G0701500)
MRC (G1000183)
Wellcome Trust (093875/Z/10/Z)
Identifiers
External DOI: https://doi.org/10.1002/jmri.25093
This record's URL: https://www.repository.cam.ac.uk/handle/1810/252960
Rights
Licence:
http://www.rioxx.net/licenses/all-rights-reserved