The primary objective is the establishment of a regional and national facility for metabolic measurements in vivo using NMR spectroscopy techniques. Specifically, the facility will focus on methods of spatial localization, assessing the utility and value of magnetic field strengths higher than those previously available in a larger bore system (4.2 Tesla, 50 cm warm bore), and determining the research and clinical potential for the less sensitive nuclei - 13C, 23Na, and the less common element 19F. The second major aim is to evaluate the existence or absence of acute or chronic biological effects of strong static magnetic fields, rapidly switched gradients super-imposed on the static field (dB/dt), and the risk from rf power deposition (heating) at the 4.2 T field. The third goal is to develop pediatric applications for the assessment of abnormal organ metabolic function and the effects of diet and therapy on such conditions. The fourth fundamental goal is the development and application of NMR methods to evaluate tumor type (are metabolic profiles specific?), and to assess the ability of 19F-labeled compounds to measure tumor temperature (as altered by hyperthermia) and the effects of various therapies. Specifically, NMR spectroscopy and imaging will be used to assess the use of perfluorocarbons and other agents as markers of vescular disruption and/or altered blood flow to a tumor region before, coincident with, and following therapy. 19F-labeled compounds are amenable to both imaging and 1-dimensional NMR studies with flat, """"""""surface"""""""" coils. This project focuses on the development and use of a high magnetic field strength system for enhanced signal-to-noise and spectral dispersion in NMR spectroscopy. It is expected that this project will provide new and basic information regarding organ metabolism and tumor metabolism. Further, that this information and the technology to be developed and applied will enhance the diagnosis and medical treatment of a number of the project's goals to the regional and national scientific community.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
1P41RR002584-01
Application #
3104172
Study Section
(SSS)
Project Start
1985-09-30
Project End
1990-09-29
Budget Start
1985-09-30
Budget End
1986-09-29
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Chiu, Tsuicheng D; Arai, Tatsuya J; Campbell Iii, James et al. (2018) MR-CBCT image-guided system for radiotherapy of orthotopic rat prostate tumors. PLoS One 13:e0198065
Mishkovsky, Mor; Anderson, Brian; Karlsson, Magnus et al. (2017) Measuring glucose cerebral metabolism in the healthy mouse using hyperpolarized 13C magnetic resonance. Sci Rep 7:11719
Moreno, Karlos X; Harrison, Crystal E; Merritt, Matthew E et al. (2017) Hyperpolarized ?-[1-13 C]gluconolactone as a probe of the pentose phosphate pathway. NMR Biomed 30:
Funk, Alexander M; Anderson, Brian L; Wen, Xiaodong et al. (2017) The rate of lactate production from glucose in hearts is not altered by per-deuteration of glucose. J Magn Reson 284:86-93
Zhang, Liang; Habib, Amyn A; Zhao, Dawen (2016) Phosphatidylserine-targeted liposome for enhanced glioma-selective imaging. Oncotarget 7:38693-38706
Walker, Christopher M; Merritt, Matthew; Wang, Jian-Xiong et al. (2016) Use of a Multi-compartment Dynamic Single Enzyme Phantom for Studies of Hyperpolarized Magnetic Resonance Agents. J Vis Exp :e53607
Wu, Yunkou; Zhang, Shanrong; Soesbe, Todd C et al. (2016) pH imaging of mouse kidneys in vivo using a frequency-dependent paraCEST agent. Magn Reson Med 75:2432-41
Malloy, Craig R; Sherry, A Dean (2016) Biochemical Specificity in Human Cardiac Imaging by 13C Magnetic Resonance Imaging. Circ Res 119:1146-1148
Moss, Lacy R; Mulik, Rohit S; Van Treuren, Tim et al. (2016) Investigation into the distinct subcellular effects of docosahexaenoic acid loaded low-density lipoprotein nanoparticles in normal and malignant murine liver cells. Biochim Biophys Acta 1860:2363-2376
Bastiaansen, Jessica A M; Merritt, Matthew E; Comment, Arnaud (2016) Measuring changes in substrate utilization in the myocardium in response to fasting using hyperpolarized [1-(13)C]butyrate and [1-(13)C]pyruvate. Sci Rep 6:25573

Showing the most recent 10 out of 374 publications