There are two main objectives of this Core. First, we intend to provide training in the use of stable isotope technology within the BTRC for use by scientists and clinicians outside the BTRC. The goal is to expand the general knowledge of how to use stable isotopes for investigation of metabolic questions in intact tissues and patients. Much of the technology, once understood, is easily transferred to most university and medical school settings in the United States. Second, we intend to disseminate the results of the work described in the TR&D projects to the clinical and scientific community. The goal is to make physicians and biomedical scientists aware of the capabilities of the technologies and to encourage use of the advances from the BTRC. To achieve these goals, we propose four specific aims.
Aim 1 is to continue to present a two-day Annual Symposium with a focus on magnetic resonance and metabolism. The first day will be refocused on training in technology and the second day will continue to present broader biological and clinical topics that are relevant to the technology developed in the BTRC.
Aim 2 is to provide training tailored to the needs of visiting scientists, students, medical housestaff and subspeciality clinical fellows as necessary to allow investigators outside the BTRC to apply the technology to clinical problems.
Aim 3 is to disseminate results and technologies via multiple strategies including a continued local Mini-Symposium for Undergraduates, continued participation in the NIH Isotope Course presented by the NIDDK, a newly proposed training course in 13C isotopomer and flux analysis at the World Molecular Imaging Congress, the web page and teaching in graduate courses.
Aim 4 is to disseminate open source software designed for experiment planning, spectral analysis and metabolic fitting of 13C tracer experiments. Together, our training and dissemination activities provide a wide range of opportunities for investigators to learn to use stable isotopes for their studies in intermediary metabolism in patients and other systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Biotechnology Resource Grants (P41)
Project #
5P41EB015908-32
Application #
9850596
Study Section
Special Emphasis Panel (ZEB1)
Project Start
Project End
Budget Start
2020-01-01
Budget End
2020-12-31
Support Year
32
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
Lux, Jacques; Sherry, A Dean (2018) Advances in gadolinium-based MRI contrast agent designs for monitoring biological processes in vivo. Curr Opin Chem Biol 45:121-130
Kaushik, Akash K; DeBerardinis, Ralph J (2018) Applications of metabolomics to study cancer metabolism. Biochim Biophys Acta Rev Cancer 1870:2-14
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
Xie, Fang; Cai, Huawei; Peng, Fangyu (2018) Anti-prostate cancer activity of 8-hydroxyquinoline-2-carboxaldehyde-thiosemicarbazide copper complexes in vivo by bioluminescence imaging. J Biol Inorg Chem :
Imakura, Yuki; Nonaka, Hiroshi; Takakusagi, Yoichi et al. (2018) Rational Design of [13 C,D14 ]Tert-butylbenzene as a Scaffold Structure for Designing Long-lived Hyperpolarized 13 C Probes. Chem Asian J 13:280-283
Kikuchi, Kazufumi; Ishimatsu, Keisuke; Zhang, Shanrong et al. (2018) Presaturation Power Adjusted Pulsed CEST: A Method to Increase Independence of Target CEST Signals. Contrast Media Mol Imaging 2018:3141789
Garda, Zoltán; Molnár, Enik?; Kálmán, Ferenc K et al. (2018) Effect of the Nature of Donor Atoms on the Thermodynamic, Kinetic and Relaxation Properties of Mn(II) Complexes Formed With Some Trisubstituted 12-Membered Macrocyclic Ligands. Front Chem 6:232
Zhou, Heling; Arias-Ramos, Nuria; López-Larrubia, Pilar et al. (2018) Oxygenation Imaging by Nuclear Magnetic Resonance Methods. Methods Mol Biol 1718:297-313
Jin, Eunsook S; Lee, Min Hee; Murphy, Rebecca E et al. (2018) Pentose phosphate pathway activity parallels lipogenesis but not antioxidant processes in rat liver. Am J Physiol Endocrinol Metab 314:E543-E551
Pérez-Malo, Marylaine; Szabó, Gergely; Eppard, Elisabeth et al. (2018) Improved Efficacy of Synthesizing *MIII-Labeled DOTA Complexes in Binary Mixtures of Water and Organic Solvents. A Combined Radio- and Physicochemical Study. Inorg Chem 57:6107-6117

Showing the most recent 10 out of 149 publications