Dynamic metabolic changes in human visual cortex in regions with positive and negative blood oxygenation level-dependent response

J Cereb Blood Flow Metab. 2019 Nov;39(11):2295-2307. doi: 10.1177/0271678X18795426. Epub 2018 Aug 17.

Abstract

Dynamic metabolic changes were investigated by functional magnetic resonance spectroscopy (fMRS) during sustained stimulation of human primary visual cortex. Two established paradigms, consisting of either a full-field or a small-circle flickering checkerboard, were employed to generate wide-spread areas of positive or negative blood oxygenation level-dependent (BOLD) responses, respectively. Compared to baseline, the glutamate concentration increased by 5.3% (p = 0.007) during activation and decreased by -3.8% (p = 0.017) during deactivation. These changes were positively correlated with the amplitude of the BOLD response (R = 0.60, p = 0.002) and probably reflect changes of tricarboxylic acid cycle activity. During deactivation, the glucose concentration decreased by -7.9% (p = 0.025) presumably suggesting increased consumption or reduced glucose supply. Other findings included an increased concentration of glutathione (4.2%, p = 0.023) during deactivation and a negative correlation of glutathione and BOLD signal changes (R = -0.49, p = 0.012) as well as positive correlations of aspartate (R = 0.44, p = 0.035) and N-acetylaspartylglutamate (R = 0.42, p = 0.035) baseline concentrations with the BOLD response. It remains to be shown in future work if the observed effects on glutamate and glucose levels deviate from the assumption of a direct link between glucose utilization and regulation of blood flow or support previous suggestions that the hemodynamic response is mainly driven by feedforward release of vasoactive messengers.

Keywords: Functional magnetic resonance spectroscopy; glucose; glutamate; negative blood oxygenation level-dependent response; positive blood oxygenation level-dependent response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Glucose / metabolism
  • Glutamic Acid / metabolism
  • Hemodynamics
  • Humans
  • Magnetic Resonance Spectroscopy / methods*
  • Oxygen / blood*
  • Oxygen Consumption / physiology
  • Visual Cortex / metabolism*

Substances

  • Glutamic Acid
  • Glucose
  • Oxygen