4.5 Article

Revisiting Glycogen Content in the Human Brain

Journal

NEUROCHEMICAL RESEARCH
Volume 40, Issue 12, Pages 2473-2481

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11064-015-1664-4

Keywords

C-13 magnetic resonance spectroscopy; Human brain; Glycogen; Mathematical modeling

Funding

  1. National Institute of Neurological Disorders and Stroke (NINDS) [R01 NS035192]
  2. National Institute of Biomedical Imaging and Bioengineering (NIBIB) [P41 EB015894]
  3. Institutional Center Cores for Advanced Neuroimaging award [P30 NS076408]
  4. National Center for Research Resources (NCRR) [S10 RR023730, S10 RR027290]
  5. CTSA [5KL2TR000113]
  6. National Center for Advancing Translational Sciences of the National Institutes of Health [UL1TR000114]

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Glycogen provides an important glucose reservoir in the brain since the concentration of glucosyl units stored in glycogen is several fold higher than free glucose available in brain tissue. We have previously reported 3-4 mu mol/g brain glycogen content using in vivo C-13 magnetic resonance spectroscopy (MRS) in conjunction with [1-C-13] glucose administration in healthy humans, while higher levels were reported in the rodent brain. Due to the slow turnover of bulk brain glycogen in humans, complete turnover of the glycogen pool, estimated to take 3-5 days, was not observed in these prior studies. In an attempt to reach complete turnover and thereby steady state C-13 labeling in glycogen, here we administered [1-C-13] glucose to healthy volunteers for 80 h. To eliminate any net glycogen synthesis during this period and thereby achieve an accurate estimate of glycogen concentration, volunteers were maintained at euglycemic blood glucose levels during [1-C-13] glucose administration and C-13-glycogen levels in the occipital lobe were measured by C-13 MRS approximately every 12 h. Finally, we fitted the data with a biophysical model that was recently developed to take into account the tiered structure of the glycogen molecule and additionally incorporated blood glucose levels and isotopic enrichments as input function in the model. We obtained excellent fits of the model to the C-13-glycogen data, and glycogen content in the healthy human brain tissue was found to be 7.8 +/- 0.3 mu mol/g, a value substantially higher than previous estimates of glycogen content in the human brain.

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