application): The function of the Mass Spectrometry Core is to provide a state-of-the-art laboratory facility for the purpose of enhancing the use of stable isotopes in nutrition research. This research will help us develop an understanding of nutrient absorption, metabolism, and turnover. Specifically, the core will be involved in mineral metabolism (mineral enrichment methodologies including modeling); measuring enrichments in biomolecules that will be sued to detect bioconversion and metabolism; gas isotope ration determinations for total energy expenditure (TEE); gas isotope ratio determinations for substrate oxidation. The Mass Spectrometry center has a long standing history at the University of Colorado Health Sciences Center, and served as an NIH Research resource facility for more than 12 years (until 1991). Through the strong bridging support of the School of Medicine and the Department of Pediatrics, we have maintained the Mass Spectrometry facility and its expert staff. The CNRU grant has provided new equipment for this core and has helped to stabilize the salary support for the most important human resources of this core. The Mass Spectrometry Core laboratory provides access to a number of state of the art mass spectrometers and trained personnel who can assist each investigator to effectively plan and implement their specific research project. This core provides an instrument (VG 7070H) and corresponding hardware for the measurement of enrichment of minerals (Fe, Cu, and ZN); three instruments (MSDs) that are dedicated to the measurements of stable isotopes in simple biomolecules (amino acids, sugars, and fats); an instrument (HP 5989A Engine) is used for developmental assays and measurement of specific target compounds; and a VG Optima gas isotope ratio mass spectrometer for both enriched CO2 and 2H determinations. However, the high expense of this equipment and the complexity of its maintenance make it impossible for an single investigator to function independent of the center. Thus, this is clearly an example of a core which extends and enhances the research opportunities of the core members.

Project Start
2000-06-01
Project End
2000-12-31
Budget Start
Budget End
Support Year
6
Fiscal Year
2000
Total Cost
$235,000
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Lee, Dustin M; Battson, Micah L; Jarrell, Dillon K et al. (2018) SGLT2 inhibition via dapagliflozin improves generalized vascular dysfunction and alters the gut microbiota in type 2 diabetic mice. Cardiovasc Diabetol 17:62
Alexeev, Erica E; Lanis, Jordi M; Kao, Daniel J et al. (2018) Microbiota-Derived Indole Metabolites Promote Human and Murine Intestinal Homeostasis through Regulation of Interleukin-10 Receptor. Am J Pathol 188:1183-1194
Beli, Eleni; Yan, Yuanqing; Moldovan, Leni et al. (2018) Restructuring of the Gut Microbiome by Intermittent Fasting Prevents Retinopathy and Prolongs Survival in db/db Mice. Diabetes 67:1867-1879
Mintz, Michael; Khair, Shanawaj; Grewal, Suman et al. (2018) Longitudinal microbiome analysis of single donor fecal microbiota transplantation in patients with recurrent Clostridium difficile infection and/or ulcerative colitis. PLoS One 13:e0190997
Keller, A C; Knaub, L A; Scalzo, R L et al. (2018) Sepiapterin Improves Vascular Reactivity and Insulin-Stimulated Glucose in Wistar Rats. Oxid Med Cell Longev 2018:7363485
Creasy, Seth A; Rynders, Corey A; Bergouignan, Audrey et al. (2018) Free-Living Responses in Energy Balance to Short-Term Overfeeding in Adults Differing in Propensity for Obesity. Obesity (Silver Spring) 26:696-702
Hildreth, Kerry L; Ozemek, Cemal; Kohrt, Wendy M et al. (2018) Vascular dysfunction across the stages of the menopausal transition is associated with menopausal symptoms and quality of life. Menopause 25:1011-1019
Beune, Irene M; Bloomfield, Frank H; Ganzevoort, Wessel et al. (2018) Consensus Based Definition of Growth Restriction in the Newborn. J Pediatr 196:71-76.e1
Rynders, Corey A; Schmidt, Stacy L; Bergouignan, Audrey et al. (2018) Effects of short-term sex steroid suppression on dietary fat storage patterns in healthy males. Physiol Rep 6:
Jensen, Thomas; Abdelmalek, Manal F; Sullivan, Shelby et al. (2018) Fructose and sugar: A major mediator of non-alcoholic fatty liver disease. J Hepatol 68:1063-1075

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