The Metabolic Physiology Shared Resource (MPSR) provides investigators with a platform for the design, execution, and interpretation of highly specialized procedures for conducting experiments in vivo. The MPSR facilitates research for investigators in species spanning from mouse to humans. Many of the basic tenets of experimental design are species-independent permitting resources and expertise to be pooled under the common MPSR umbrella. This philosophy alleviates experimental constraints by providing access to a variety of model systems and provides for seamless translation of basic experimental findings to humans. The MPSR uses a defined mechanism for the design and optimization of experimental protocols using an established Studio format. The Studio (i) brings together Vanderbilt scientists with specific expertise to review a proposal; (ii) identifies potential limitations on the front-end; and (iii) leads to the most efficient use of resources including animals and human volunteers. The MPSR makes complex in vivo experiments feasible by providing specialized animal surgical (e.g. catheter placement, bariatric surgery) and experimental (e.g. clamps, energy balance) services. Advancements in the present cycle have led to the development of bariatric surgery procedures and expansion of resources for energy balance measurements in animals that parallel procedures used in human studies conducted by the MPSR. The MPSR has also added a human clamp component. The addition of these vital services fills out the scope of services leading to comprehensive analyses of insulin action and energy balance from rodents to large animals to human subjects. MPSR services will channel into analytical, statistical, and bioinformatics services, thereby enhancing the utility of this resource.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK020593-42
Application #
9691329
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
42
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
079917897
City
Nashville
State
TN
Country
United States
Zip Code
37232
Dutter, Brendan F; Ender, Anna; Sulikowski, Gary A et al. (2018) Rhodol-based thallium sensors for cellular imaging of potassium channel activity. Org Biomol Chem 16:5575-5579
Horwitz, Elad; Krogvold, Lars; Zhitomirsky, Sophia et al. (2018) ?-Cell DNA Damage Response Promotes Islet Inflammation in Type 1 Diabetes. Diabetes 67:2305-2318
Herrick, Mary K; Favela, Kristin M; Simerly, Richard B et al. (2018) Attenuation of diet-induced hypothalamic inflammation following bariatric surgery in female mice. Mol Med 24:56
Martinez 2nd, Keith A; Romano-Keeler, Joann; Zackular, Joseph P et al. (2018) Bacterial DNA is present in the fetal intestine and overlaps with that in the placenta in mice. PLoS One 13:e0197439
Perez, Katia M; Curley, Kathleen L; Slaughter, James C et al. (2018) Glucose Homeostasis and Energy Balance in Children With Pseudohypoparathyroidism. J Clin Endocrinol Metab 103:4265-4274
Saunders, Diane C; Brissova, Marcela; Phillips, Neil et al. (2018) Ectonucleoside Triphosphate Diphosphohydrolase-3 Antibody Targets Adult Human Pancreatic ? Cells for In Vitro and In Vivo Analysis. Cell Metab :
Marre, Meghan L; McGinty, John W; Chow, I-Ting et al. (2018) Modifying Enzymes Are Elicited by ER Stress, Generating Epitopes That Are Selectively Recognized by CD4+ T Cells in Patients With Type 1 Diabetes. Diabetes 67:1356-1368
Wang, Feng; Katagiri, Daisuke; Li, Ke et al. (2018) Assessment of renal fibrosis in murine diabetic nephropathy using quantitative magnetization transfer MRI. Magn Reson Med 80:2655-2669
Creecy, Amy; Uppuganti, Sasidhar; Unal, Mustafa et al. (2018) Low bone toughness in the TallyHO model of juvenile type 2 diabetes does not worsen with age. Bone 110:204-214
Santos Guasch, Gabriela L; Beeler, J Scott; Marshall, Clayton B et al. (2018) p73 Is Required for Ovarian Follicle Development and Regulates a Gene Network Involved in Cell-to-Cell Adhesion. iScience 8:236-249

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