- Animal Model Research Core: The goal of the Animal Model Research (AMR) Core facility of the NORC is to facilitate the nutritional and obesity-related research of investigators using animal models to generate translational and hopefully transformational insight into human disease. Since its founding in 1999, the Core has continually evolved by modifying existing services, introducing new services, and providing extensive training to investigators in state- of-the-art techniques for animal phenotyping relevant to nutrition and obesity. We now focus on the following seven critical Core services: 1) Provision of mouse models relevant to nutritional and obesity research; 2) Biochemical analysis of serum samples; 3) Biochemical analysis of tissue lipids; 4) Molecular analyses of gene expression using quantitative RT-PCR; 5) Body composition analyses; 6) Energy metabolism and balance; and 7) Consultation and training. During this last funding period, the Core added a new Associate Director, hired a new lab manager, streamlined operations to allow ready access of crticial equipment to the user base, brought online new metabolic phenotyping (TSE Phenomaster) instrumentation and mRNA analysis instrumentation (both with supplemental institutional support), completely upgraded our body composition instrumentation (also with supplemental institutional support), and enhanced the training capabilites of the Core. These improvements attracted 20 new investigators to the Core, successfully assisted 15 Pilot and Feasibilty recipients in obtaining independent grant support, and helped fuel an impressive range of discovery research in nutrition/obesity, including studies of the microbiota in obesity and the role of nutrition in reproduction, lipid metabolism, atherosclerosis, and bone health. Through joint operations with the Mouse Phenotyping Core of the NIDDK-funded Diabetes Research Center (DRC) at Washington University, the Animal Model Core enjoys synergies through collaborative interactions, shared staff, volume discounts in reagents, and shared institutional investments to provide cost-effective and efficient services for NORC investigators.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK056341-18
Application #
9462079
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
18
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Riek, Amy E; Oh, Jisu; Darwech, Isra et al. (2018) Vitamin D3 supplementation decreases a unique circulating monocyte cholesterol pool in patients with type 2 diabetes. J Steroid Biochem Mol Biol 177:187-192
Bittel, Adam J; Bohnert, Kathryn L; Reeds, Dominic N et al. (2018) Reduced Muscle Strength in Barth Syndrome May Be Improved by Resistance Exercise Training: A Pilot Study. JIMD Rep :
Shepherd, Andrew J; Copits, Bryan A; Mickle, Aaron D et al. (2018) Angiotensin II Triggers Peripheral Macrophage-to-Sensory Neuron Redox Crosstalk to Elicit Pain. J Neurosci 38:7032-7057
Cifarelli, Vincenza; Abumrad, Nada A (2018) Intestinal CD36 and Other Key Proteins of Lipid Utilization: Role in Absorption and Gut Homeostasis. Compr Physiol 8:493-507
Smith, Gordon I; Commean, Paul K; Reeds, Dominic N et al. (2018) Effect of Protein Supplementation During Diet-Induced Weight Loss on Muscle Mass and Strength: A Randomized Controlled Study. Obesity (Silver Spring) 26:854-861
Perry, Justin S A; Russler-Germain, Emilie V; Zhou, You W et al. (2018) Transfer of Cell-Surface Antigens by Scavenger Receptor CD36 Promotes Thymic Regulatory T Cell Receptor Repertoire Development and Allo-tolerance. Immunity 48:1271
Turecamo, S E; Walji, T A; Broekelmann, T J et al. (2018) Contribution of metabolic disease to bone fragility in MAGP1-deficient mice. Matrix Biol 67:1-14
Samovski, Dmitri; Dhule, Pallavi; Pietka, Terri et al. (2018) Regulation of Insulin Receptor Pathway and Glucose Metabolism by CD36 Signaling. Diabetes 67:1272-1284
Porter, Lane C; Franczyk, Michael P; Pietka, Terri et al. (2018) NAD+-dependent deacetylase SIRT3 in adipocytes is dispensable for maintaining normal adipose tissue mitochondrial function and whole body metabolism. Am J Physiol Endocrinol Metab 315:E520-E530
Acevedo, María Belén; Eagon, J Christopher; Bartholow, Bruce D et al. (2018) Sleeve gastrectomy surgery: when 2 alcoholic drinks are converted to 4. Surg Obes Relat Dis 14:277-283

Showing the most recent 10 out of 1334 publications