The overall objective of this work is to further our understanding of the relationship between changes in brain cellular activity, caused by the functional activity of the brain in neurologically normal humans, and changes in blood flow and metabolism. Everyone agrees that the resting brain metabolizes glucose aerobically as its main source of energy. On the basis it was assumed that changes in the activity of the brain would be accompanied by parallel changes in blood glow, glucose utilization and oxygen consumption. It came as a considerable surprise when work with positron emission tomography (PET), supported previously under this program project [Fox, 1986#18][Fox, 1988#19], revealed parallel changes in glucose utilization and blood flow unaccompanied by changes in oxygen consumption. This important observation has not only catalyzed a re- evaluation of these relationships but also provided the physiological rationale for functional mapping of the human brain with magnetic resonance imaging (MRI). Despite the immense interest in functional mapping of the brain, uncertainty surrounds our understanding of these functionally-induced metabolic and circulatory changes. This project addresses two central questions concerning that understanding. First, do the changes in blood flow exceed those of oxygen consumption simply to maintain adequate tissue oxygen. To answer this question we propose to examine blood flow responses as a function of oxygen availability. Second, if glucose is used but only metabolized to lactate, why don't tissue lactate levels adequately reflect the increased glycolysis? To answer this question we propose to determine whether lactate egress from brain is facilitated in areas of increased functional activity. These experiments will provide valuable new information on the relationship of brain functional activity to brain energy metabolism in neurologically normal humans and a sounder scientific basis for functional brain imaging with PET and fMRI.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL013851-36
Application #
6202155
Study Section
Project Start
1999-07-01
Project End
2000-06-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
36
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
Peterson, Linda R; Herrero, Pilar; Coggan, Andrew R et al. (2015) Type 2 diabetes, obesity, and sex difference affect the fate of glucose in the human heart. Am J Physiol Heart Circ Physiol 308:H1510-6
Zhou, Dong; Chu, Wenhua; Xu, Jinbin et al. (2014) Synthesis, [¹?F] radiolabeling, and evaluation of poly (ADP-ribose) polymerase-1 (PARP-1) inhibitors for in vivo imaging of PARP-1 using positron emission tomography. Bioorg Med Chem 22:1700-7
Gropler, Robert J (2014) Trying to prevent diabetic cardiovascular autonomic neuropathy: more questions than answers. J Nucl Cardiol 21:842-4
Lyons, Matthew R; Peterson, Linda R; McGill, Janet B et al. (2013) Impact of sex on the heart's metabolic and functional responses to diabetic therapies. Am J Physiol Heart Circ Physiol 305:H1584-91
Herrero, Pilar; Laforest, Richard; Shoghi, Kooresh et al. (2012) Feasibility and dosimetry studies for 18F-NOS as a potential PET radiopharmaceutical for inducible nitric oxide synthase in humans. J Nucl Med 53:994-1001
Gropler, Robert J (2012) The road connecting obesity and coronary vasomotor function: straight line or U-turn? JACC Cardiovasc Imaging 5:816-8
Solingapuram Sai, Kiran Kumar; Kil, Kun-Eek; Tu, Zhude et al. (2012) Synthesis, radiolabeling and initial in vivo evaluation of [(11)C]KSM-01 for imaging PPAR-? receptors. Bioorg Med Chem Lett 22:6233-6
Cheng, Ju-Chieh Kevin; Shoghi, Kooresh; Laforest, Richard (2012) Quantitative accuracy of MAP reconstruction for dynamic PET imaging in small animals. Med Phys 39:1029-41
Peterson, Linda R; Saeed, Ibrahim M; McGill, Janet B et al. (2012) Sex and type 2 diabetes: obesity-independent effects on left ventricular substrate metabolism and relaxation in humans. Obesity (Silver Spring) 20:802-10
Zhou, Dong; Chu, Wenhua; Dence, Carmen S et al. (2012) Highly efficient click labeling using 2-[¹?F]fluoroethyl azide and synthesis of an ¹?FN-hydroxysuccinimide ester as conjugation agent. Nucl Med Biol 39:1175-81

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