Research ReportBrain metabolite concentrations across cortical regions in healthy adults

Magnetic resonance spectroscopy (MRS) can provide in vivo information about metabolite levels across multiple brain regions. This study used MRS to examine concentrations of N-acetylaspartate (NAA), a marker of neuronal integrity and function, and choline (Cho), which is related to the amount of cell membrane per unit volume, in anterior cingulate cortex (ACC) and parieto-occipital cortex (POC) in healthy individuals. Data were drawn from two experiments which examined glutamatergic and GABAergic signaling in schizophrenia and bipolar disorder. After controlling for gray matter percentages, NAA/creatine (Cr) was 18% higher in POC than in ACC (p < 0.001); Cho/Cr was 46% lower in POC than in ACC (p < 0.001). There was an effect of study (p < 0.001 for both metabolites), but no region by study interaction (NAA p = 0.101, Cho p = 0.850). Since NAA is localized to the intracellular space, these data suggest that ACC neuronal compartment is reduced as compared with POC, or that there is a lower concentration of NAA per cell in the ACC than POC, or both. Since elevated Cho suggests more cell membrane per unit volume, reduced NAA in ACC appears to be coupled with increases in overall cell membrane compartment. These findings are consistent with a number of previous studies using proton MRS which found increasing NAA and decreasing Cho moving caudally, and with postmortem anatomical studies which found neurons in more widely spaced bundles in ACC when compared to parietal and occipital cortices. MRS may be a useful tool for studying physical properties of the living human brain.

Research Highlights► NAA/Cr was 18% higher; Cho/Cr was 46% lower in POC than in ACC (p < 0.001 for each). ►This suggests lower membrane density and higher neuronal volume in POC. ► This could point to a reduction in the complexity of neuronal profiles. ► These findings are consistent with previous anatomical and proton MRS studies. ► MRS may provide in vivo measures reflecting the brain's cellular properties.