Uniform distributions of glucose oxidation and oxygen extraction in gray matter of normal human brain: No evidence of regional differences of aerobic glycolysis
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Uniform distributions of glucose oxidation and oxygen extraction in gray matter of normal human brain : No evidence of regional differences of aerobic glycolysis. / Hyder, Fahmeed; Herman, Peter; Bailey, Christopher J.; Møller, Arne; Globinsky, Ronen; Fulbright, Robert K; Rothman, Douglas L; Gjedde, Albert.
In: Journal of Cerebral Blood Flow and Metabolism, Vol. 36, No. 5, 2016, p. 903-916.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Uniform distributions of glucose oxidation and oxygen extraction in gray matter of normal human brain
T2 - No evidence of regional differences of aerobic glycolysis
AU - Hyder, Fahmeed
AU - Herman, Peter
AU - Bailey, Christopher J.
AU - Møller, Arne
AU - Globinsky, Ronen
AU - Fulbright, Robert K
AU - Rothman, Douglas L
AU - Gjedde, Albert
N1 - © The Author(s) 2016.
PY - 2016
Y1 - 2016
N2 - Regionally variable rates of aerobic glycolysis in brain networks identified by resting-state functional magnetic resonance imaging (R-fMRI) imply regionally variable adenosine triphosphate (ATP) regeneration. When regional glucose utilization is not matched to oxygen delivery, affected regions have correspondingly variable rates of ATP and lactate production. We tested the extent to which aerobic glycolysis and oxidative phosphorylation power R-fMRI networks by measuring quantitative differences between the oxygen to glucose index (OGI) and the oxygen extraction fraction (OEF) as measured by positron emission tomography (PET) in normal human brain (resting awake, eyes closed). Regionally uniform and correlated OEF and OGI estimates prevailed, with network values that matched the gray matter means, regardless of size, location, and origin. The spatial agreement between oxygen delivery (OEF≈0.4) and glucose oxidation (OGI ≈ 5.3) suggests that no specific regions have preferentially high aerobic glycolysis and low oxidative phosphorylation rates, with globally optimal maximum ATP turnover rates (VATP ≈ 9.4 µmol/g/min), in good agreement with (31)P and (13)C magnetic resonance spectroscopy measurements. These results imply that the intrinsic network activity in healthy human brain powers the entire gray matter with ubiquitously high rates of glucose oxidation. Reports of departures from normal brain-wide homogeny of oxygen extraction fraction and oxygen to glucose index may be due to normalization artefacts from relative PET measurements.
AB - Regionally variable rates of aerobic glycolysis in brain networks identified by resting-state functional magnetic resonance imaging (R-fMRI) imply regionally variable adenosine triphosphate (ATP) regeneration. When regional glucose utilization is not matched to oxygen delivery, affected regions have correspondingly variable rates of ATP and lactate production. We tested the extent to which aerobic glycolysis and oxidative phosphorylation power R-fMRI networks by measuring quantitative differences between the oxygen to glucose index (OGI) and the oxygen extraction fraction (OEF) as measured by positron emission tomography (PET) in normal human brain (resting awake, eyes closed). Regionally uniform and correlated OEF and OGI estimates prevailed, with network values that matched the gray matter means, regardless of size, location, and origin. The spatial agreement between oxygen delivery (OEF≈0.4) and glucose oxidation (OGI ≈ 5.3) suggests that no specific regions have preferentially high aerobic glycolysis and low oxidative phosphorylation rates, with globally optimal maximum ATP turnover rates (VATP ≈ 9.4 µmol/g/min), in good agreement with (31)P and (13)C magnetic resonance spectroscopy measurements. These results imply that the intrinsic network activity in healthy human brain powers the entire gray matter with ubiquitously high rates of glucose oxidation. Reports of departures from normal brain-wide homogeny of oxygen extraction fraction and oxygen to glucose index may be due to normalization artefacts from relative PET measurements.
KW - Adenosine Triphosphate/metabolism
KW - Brain/metabolism
KW - Glucose/analysis
KW - Glycolysis/physiology
KW - Gray Matter/metabolism
KW - Humans
KW - Magnetic Resonance Imaging
KW - Male
KW - Oxidation-Reduction
KW - Oxidative Phosphorylation
KW - Oxygen/analysis
KW - Positron-Emission Tomography
U2 - 10.1177/0271678X15625349
DO - 10.1177/0271678X15625349
M3 - Journal article
C2 - 26755443
VL - 36
SP - 903
EP - 916
JO - Journal of Cerebral Blood Flow and Metabolism
JF - Journal of Cerebral Blood Flow and Metabolism
SN - 0271-678X
IS - 5
ER -
ID: 202511985