Diabetes is highly prevalent in the United States and is associated with increased morbidity from cardiovascular, renal, neurological and other complications. Our understanding of the pathogenesis of diabetes has benefited immensely from pharmacological, dietary and genetic manipulations in mice and other rodents. Despite the rapid increase in the use of gene targeting methodology to elucidate the molecular mechanisms mediating diabetes in mice, such efforts are often hampered by the absence of a clear phenotype. Failure to demonstrate a phenotype is attributable in part to the lack of expertise and/or facilities for evaluating physiologic and metabolic features in mice. We propose to establish a Mouse Phenotyping, Physiology and Metabolism Core, with the objective of providing investigators of the Penn Diabetes Center with state-of-the-art, timely and cost-effective diagnostic studies in mice. The core will offer services for analyzing glucose homeostasis, feeding behavior and energy balance, body composition, blood chemistry and hemodynamics. Activities of the core will be carried out by 2 technicians under the direction of Dr. Rex Ahima. The Phenotyping Core will maintain a databank of physiological, hormonal and metabolic measurements in mouse models of diabetes and obesity, and offer advice and training on various aspects of mouse physiology. Activities of the core will be coordinated with other core laboratories, Le Islet Cell Biology (Franz Matschinsky), Radioimmunoassay (Bryan Wolf), Transgenic and Chimeric (Nancy Cooke and Functional Genomics (Klaus Kaestner). These efforts will result in optimum data acquisition in diabetic mouse models, and facilitate the translation of ideas from the bench to mice and ultimately 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 #
2P30DK019525-26
Application #
6503275
Study Section
Special Emphasis Panel (ZDK1)
Project Start
1977-03-01
Project End
2007-02-28
Budget Start
Budget End
Support Year
26
Fiscal Year
2002
Total Cost
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
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
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
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
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
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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