MOUSE PHENOTYPING, PHYSIOLOGY, AND METABOLISM CORE: Director - R. AhimaOur understanding of the pathogenesis of diabetes has benefited from the use of gene targetingmethodology in mice to elucidate molecular mechanisms. However, such efforts are oftenhampered by an absence of a clear metabolic phenotype. Failure to identify a phenotype may bedue to lack of expertise and/or facilities for evaluating metabolic changes in mice. The MousePhenotyping, Physiology and Metabolism Core provides investigators of the Penn Diabetes andEndocrinology Research Center (DERC) with state-of-the-art, timely and cost-effective diagnosticstudies in mice. The core offers consultation and experimental design, monitoring of feeding,energy expenditure and locomotor activity using the Comprehensive Laboratory Animal MonitoringSystem (CLAMS), treadmill exercise using the Oxymax system, and measurement of bodycomposition using dual emission x-ray absorptiometry (DEXA) and carcass chemistry. Glucosehomeostasis is assessed by oral or intraperitoneal (i.p.) glucose administration, and whole bodyinsulin sensitivity by i.p. insulin injection. Insulin clamp and radioactive tracers are used to assessglucose fluxes and tissue specific glucose uptake. Studies in the core are performed by tworesearch specialists under the direction of Rex Ahima. Future plans for the core include the usemagnetic resonance (MRI) for measurement of water, lean and fat content, assessment of in vivolipid kinetics, and employment of an additional technician to expedite services. The MousePhenotyping, Physiology and Metabolism Core will maintain a databank of metabolic and hormonalparameters in mouse models of diabetes and obesity, and coordinate its activities with other corelaboratories, i.e. Islet Cell Biology (Franz Matschinsky), Radioimmunoassay/Biomarkers (BryanWolf; Muredach Reilly), Transgenic and Chimeric Mouse (Nancy Cooke), and Genomics and GeneTargeting Cores (Klaus Kaestner). These efforts will result in optimum data acquisition andmetabolic phenotyping of mice, and facilitate the translation of ideas from the bench to mice, andultimately to humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK019525-31
Application #
7284633
Study Section
Special Emphasis Panel (ZDK1-GRB-N (J1))
Project Start
2007-04-01
Project End
2012-03-31
Budget Start
2007-05-15
Budget End
2008-03-31
Support Year
31
Fiscal Year
2007
Total Cost
$172,992
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Rickels, Michael R; Peleckis, Amy J; Dalton-Bakes, Cornelia et al. (2018) Continuous Glucose Monitoring for Hypoglycemia Avoidance and Glucose Counterregulation in Long-Standing Type 1 Diabetes. J Clin Endocrinol Metab 103:105-114
Guan, Dongyin; Xiong, Ying; Borck, Patricia C et al. (2018) Diet-Induced Circadian Enhancer Remodeling Synchronizes Opposing Hepatic Lipid Metabolic Processes. Cell 174:831-842.e12
Jang, Cholsoon; Chen, Li; Rabinowitz, Joshua D (2018) Metabolomics and Isotope Tracing. Cell 173:822-837
Shoshkes-Carmel, Michal; Wang, Yue J; Wangensteen, Kirk J et al. (2018) Subepithelial telocytes are an important source of Wnts that supports intestinal crypts. Nature 557:242-246
Ibrahim, Fadia; Maragkakis, Manolis; Alexiou, Panagiotis et al. (2018) Ribothrypsis, a novel process of canonical mRNA decay, mediates ribosome-phased mRNA endonucleolysis. Nat Struct Mol Biol 25:302-310
Condon, David E; Tran, Phu V; Lien, Yu-Chin et al. (2018) Defiant: (DMRs: easy, fast, identification and ANnoTation) identifies differentially Methylated regions from iron-deficient rat hippocampus. BMC Bioinformatics 19:31
Cooney, Laura G; Milman, Lauren W; Hantsoo, Liisa et al. (2018) Cognitive-behavioral therapy improves weight loss and quality of life in women with polycystic ovary syndrome: a pilot randomized clinical trial. Fertil Steril 110:161-171.e1
Williams, Bianca; Correnti, Jason; Oranu, Amanke et al. (2018) A novel role for ceramide synthase 6 in mouse and human alcoholic steatosis. FASEB J 32:130-142
Correnti, Jason M; Gottshall, Lauren; Lin, Annie et al. (2018) Ethanol and C2 ceramide activate fatty acid oxidation in human hepatoma cells. Sci Rep 8:12923
Qiu, Chengxiang; Huang, Shizheng; Park, Jihwan et al. (2018) Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease. Nat Med 24:1721-1731

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