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In vivo γ‐aminobutyric acid measurement in rats with spectral editing at 4.7T

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: Spect...

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Detalles Bibliográficos
Autores principales: Sawiak, Stephen J., Jupp, Bianca, Taylor, Tom, Caprioli, Daniele, Carpenter, T. Adrian, Dalley, Jeffrey W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869682/
https://www.ncbi.nlm.nih.gov/pubmed/26633759
http://dx.doi.org/10.1002/jmri.25093
Descripción
Sumario: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 mm(3) (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 2016;43:1308–1312.