- Animal Studies Core As it has for over a decade, the fee-for-service MDRC Animal Studies Core (ASC) (previously, the Animal Phenotyping Core- APC) provides state-of-the art equipment, services, training, and consultation regarding the detailed metabolic phenotyping of mouse and rat models of metabolic disease. T o address the previously unmet needs of MDRC members , the MDRC has invested in new technology and established a host of new services over the past five years . The ASC will continue to support these technologies and services, providing access to crucial equipment, expertise and training to empower specialized studies of rodent models of diabetes and related diseases. The ASC consists of four labs: 1) The Rat Metabolic Phenotyping Lab: includes the assessment of glucose homeostasis, whole animal metabolic assessment, body composition, and other specialized metabolic assessments in rats. 2) The Optogenetics and Behavioral Phenotyping Lab: provides training and access to optogenetic equipment to examine physiologic and behavioral responses to neural circuit manipulation, as well as with equipment to measure relevant behaviors, such as homeostatic and non-homeostatic feeding, activity, reward, and other behaviors that impact and/or are regulated by metabolic parameters in rodents. 3) The Continuous Glucose Monitoring Lab: provides continuous assessment of blood glucose concentrations in conscious, unrestrained rodents by radiotelemetry. This technology minimizes the stress of handling rodents and permits a detailed analysis of glucose fluctuations within normal feeding patterns and across extended time-frames. 4) The Islet Lab: provides islet isolation from mice and rats and ex vivo studies (including perifusion) of islets and other endocrine tissues. The ASC directly supports the goals of the MDRC. The services that the ASC provide are unique and are an important means to study rodent models of diabetes and related diseases, without which crucial aspects of diabetes-related research could not be accomplished. This core provides the necessary i nfrastructure to perform advanced, standardized, metabolic phenotyping of animal models of diabetes and related disorders that arise from genetic, pharmacologic, dietary, or other perturbations. The centralized equipment and services expedites research for many MDRC investigators in a cost-effective manner and provides access to complex metabolic techniques that they may not have otherwise.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK020572-44
Application #
10071172
Study Section
Special Emphasis Panel (ZDK1)
Project Start
2019-12-01
Project End
2022-11-30
Budget Start
2020-12-01
Budget End
2021-11-30
Support Year
44
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Steyn, Frederik J; Ngo, Shyuan T; Chen, Vicky Ping et al. (2018) 17?-estradiol acts through hypothalamic pro-opiomelanocortin expressing neurons to reduce feeding behavior. Aging Cell 17:
Schofield, Heather K; Tandon, Manuj; Park, Min-Jung et al. (2018) Pancreatic HIF2? Stabilization Leads to Chronic Pancreatitis and Predisposes to Mucinous Cystic Neoplasm. Cell Mol Gastroenterol Hepatol 5:169-185.e2
Zhao, Xu-Yun; Xiong, Xuelian; Liu, Tongyu et al. (2018) Long noncoding RNA licensing of obesity-linked hepatic lipogenesis and NAFLD pathogenesis. Nat Commun 9:2986
Kim, Geun Hyang; Shi, Guojun; Somlo, Diane Rm et al. (2018) Hypothalamic ER-associated degradation regulates POMC maturation, feeding, and age-associated obesity. J Clin Invest 128:1125-1140
Elenbaas, Jared S; Bragazzi Cunha, Juliana; Azuero-Dajud, Rodrigo et al. (2018) Lamin A/C Maintains Exocrine Pancreas Homeostasis by Regulating Stability of RB and Activity of E2F. Gastroenterology 154:1625-1629.e8
Herman, William H; Pan, Qing; Edelstein, Sharon L et al. (2018) Erratum. Impact of Lifestyle and Metformin Interventions on the Risk of Progression to Diabetes and Regression to Normal Glucose Regulation in Overweight or Obese People With Impaired Glucose Regulation. Diabetes Care 2017;40:1668-1677. Diabetes Care 41:913
Rajala, Ammaji; Wang, Yuhong; Abcouwer, Steven F et al. (2018) Developmental and light regulation of tumor suppressor protein PP2A in the retina. Oncotarget 9:1505-1523
McCabe, Laura R; Parameswaran, Narayanan (2018) Advances in Probiotic Regulation of Bone and Mineral Metabolism. Calcif Tissue Int 102:480-488
Wood, Landon; Roelofs, Karen; Koch, Lauren G et al. (2018) Vertical sleeve gastrectomy corrects metabolic perturbations in a low-exercise capacity rat model. Mol Metab 11:189-196
Kycia, Ina; Wolford, Brooke N; Huyghe, Jeroen R et al. (2018) A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression. Am J Hum Genet 102:620-635

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