Measurement of CMRO2 and its relationship with CBF in hypoxia with an extended calibrated BOLD method

J Cereb Blood Flow Metab. 2020 Oct;40(10):2066-2080. doi: 10.1177/0271678X19885124. Epub 2019 Oct 30.

Abstract

Cerebral blood flow (CBF) and cerebral metabolic rate of oxygen (CMRO2) are physiological parameters that not only reflect brain health and disease but also jointly contribute to blood oxygen level-dependent (BOLD) signals. Nevertheless, unsolved issues remain concerning the CBF-CMRO2 relationship in the working brain under various oxygen conditions. In particular, the CMRO2 responses to functional tasks in hypoxia are less studied. We extended the calibrated BOLD model to incorporate CMRO2 measurements in hypoxia. The extended model, which was cross-validated with a multicompartment BOLD model, considers the influences of the reduced arterial saturation level and increased baseline cerebral blood volume (CBV) and deoxyhemoglobin concentration on the changes of BOLD signals in hypoxia. By implementing a pulse sequence to simultaneously acquire the CBV-, CBF- and BOLD-weighted signals, we investigated the effects of mild hypoxia on the CBF and CMRO2 responses to graded visual stimuli. Compared with normoxia, mild hypoxia caused significant alterations in both the amplitude and the trend of the CMRO2 responses but did not impact the corresponding CBF responses. Our observations suggested that the flow-metabolism coupling strategies in the brain during mild hypoxia were different from those during normoxia.

Keywords: Blood oxygen level-dependent; cerebral blood flow; cerebral metabolic rate of oxygen; flow-metabolism; hypoxia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Algorithms
  • Blood Volume / physiology
  • Brain Chemistry / physiology
  • Brain Mapping
  • Cerebrovascular Circulation*
  • Female
  • Hemoglobins / metabolism
  • Humans
  • Hypoxia, Brain / metabolism*
  • Hypoxia, Brain / physiopathology*
  • Kinetics
  • Magnetic Resonance Imaging / methods*
  • Male
  • Oxygen / blood
  • Oxygen Consumption*
  • Reproducibility of Results
  • Young Adult

Substances

  • Hemoglobins
  • deoxyhemoglobin
  • Oxygen