Functional brain imaging is based upon the assumption that localized changes in brain circulation(i.e., blood flow, blood volume, vascular mean transit time) and metabolism accurately reflect changes in neuronal activity. Positron emission tomography (PET) and magnetic resonance imaging (MRI) are able to measure changes in circulation and metabolism safely and accurately to provide a unique window into human brain function. However, our understanding of the relationship of brain circulation and metabolism to neuronal activity is incomplete as is our understanding of the respective roles of PET and MRI in investigating these issues. It is the purpose of this project to employ PET, MRI and magnetic resonance spectroscopy (MRS) together in normal human subjects as well as patients with selected diseases to obtain a more complete understanding of the basis for the signals obtained and the respective role to be played by PET and MRI in functional brain imaging. This project compliments work in the project by powers which explores in detail the relationship of brain function to the delivery, transport and metabolism of glucose. This project will also be important to the work in the project by Peterson where the role of MRI has yet to be determined. Finally, this project brings together the expertise and resources of 3 major research groups whose combined experience in functional brain imaging with PET (Raichle an Powers), MRI (Haacke and Lin) and MRS (Ackerman, Neil and Bretthorst) is unique and should ensure that significant new scientific information regarding human brain function will be forthcoming from the proposed studies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center (P50)
Project #
5P50NS006833-33
Application #
6111999
Study Section
Project Start
1998-12-01
Project End
2000-04-14
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
33
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Goyal, Manu S; Vlassenko, Andrei G; Blazey, Tyler M et al. (2017) Loss of Brain Aerobic Glycolysis in Normal Human Aging. Cell Metab 26:353-360.e3
Shannon, Benjamin J; Vaishnavi, Sanjeev Neil; Vlassenko, Andrei G et al. (2016) Brain aerobic glycolysis and motor adaptation learning. Proc Natl Acad Sci U S A 113:E3782-91
Wig, Gagan S; Laumann, Timothy O; Cohen, Alexander L et al. (2014) Parcellating an individual subject's cortical and subcortical brain structures using snowball sampling of resting-state correlations. Cereb Cortex 24:2036-54
Goyal, Manu S; Hawrylycz, Michael; Miller, Jeremy A et al. (2014) Aerobic glycolysis in the human brain is associated with development and neotenous gene expression. Cell Metab 19:49-57
Powers, William J (2014) William M. Feinberg award for excellence in clinical stroke: hemodynamics and stroke risk in carotid artery occlusion. Stroke 45:3123-8
Glasser, Matthew F; Goyal, Manu S; Preuss, Todd M et al. (2014) Trends and properties of human cerebral cortex: correlations with cortical myelin content. Neuroimage 93 Pt 2:165-75
Power, Jonathan D; Mitra, Anish; Laumann, Timothy O et al. (2014) Methods to detect, characterize, and remove motion artifact in resting state fMRI. Neuroimage 84:320-41
Duchek, Janet M; Balota, David A; Thomas, Jewell B et al. (2013) Relationship between Stroop performance and resting state functional connectivity in cognitively normal older adults. Neuropsychology 27:516-28
Wang, Liang; Brier, Matthew R; Snyder, Abraham Z et al. (2013) Cerebrospinal fluid A?42, phosphorylated Tau181, and resting-state functional connectivity. JAMA Neurol 70:1242-8
Shannon, B J; Dosenbach, R A; Su, Y et al. (2013) Morning-evening variation in human brain metabolism and memory circuits. J Neurophysiol 109:1444-56

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