The objectives of this research effort are the assessment, in vivo, and regionally of metabolic pathways in various organs, particularly the brain and the heart, by following the fate of radioactively-labeled metabolic substrates. The ultimate goals of this investigation are to develop and apply methods for the in vivo and regional measure of physiological processes which will be ultimately applied to the understanding of basic biological processes and to the understanding and diagnosis of pathology. The proposed approach consists of labeling selected metabolic substrates or other molecules of importance in physiological processes with a radioactive nuclide, the decay of which result inthe generation of high energy electromagnetic radiation. After the administration of the substrate to the subject under the study, the location of the nuclide, as a function of time, is followed by externally placed detectors, or more often, by positron emission tomography (PET), and the metabolic pathway under study is unraveled through the application of a suitable mathematical model. For this purpose, the labels must be with few exception, nuclide akin to those found in the chemical structure of living matter. We propose to use carbon-11, nitrogen-13, oxygen-15, and in some instances, in the labeling of substrate analogs, fluorine-18. These nuclides are prepared by a cyclotron located n our medical center. All of them decay with the emission of positrons, which, as they are absorbed, generate the annihilation radiation which is used in generating """"""""functional images."""""""" The program is divided into three areas: (1) chemical investigations; (2) neurological studies; and (3) cardiovascular studies. The above three projects share the common CORE facilities and are extensively cross linked by the methodology used.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL013851-23
Application #
3097487
Study Section
Heart, Lung, and Blood Research Review Committee A (HLBA)
Project Start
1976-06-01
Project End
1987-02-28
Budget Start
1985-03-01
Budget End
1986-02-28
Support Year
23
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Washington University
Department
Type
Schools of Medicine
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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