- 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 #
2P30DK020572-41
Application #
9443253
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2018-02-27
Budget End
2018-11-30
Support Year
41
Fiscal Year
2018
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
Yu, Jingcheng; Koenig, Ronald J (2018) Thyroid-Specific PPAR? Deletion Is Benign in the Mouse. Endocrinology 159:1463-1468
Griffin, Cameron; Eter, Leila; Lanzetta, Nico et al. (2018) TLR4, TRIF, and MyD88 are essential for myelopoiesis and CD11c+ adipose tissue macrophage production in obese mice. J Biol Chem 293:8775-8786
Jun, Goo; Manning, Alisa; Almeida, Marcio et al. (2018) Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proc Natl Acad Sci U S A 115:379-384
Perkins, Bruce A; Lovblom, Leif E; Bril, Vera et al. (2018) Corneal confocal microscopy for identification of diabetic sensorimotor polyneuropathy: a pooled multinational consortium study. Diabetologia 61:1856-1861
Pearson, Gemma; Chai, Biaoxin; Vozheiko, Tracy et al. (2018) Clec16a, Nrdp1, and USP8 Form a Ubiquitin-Dependent Tripartite Complex That Regulates ?-Cell Mitophagy. Diabetes 67:265-277
Wang, Luhong; Burger, Laura L; Greenwald-Yarnell, Megan L et al. (2018) Glutamatergic Transmission to Hypothalamic Kisspeptin Neurons Is Differentially Regulated by Estradiol through Estrogen Receptor ? in Adult Female Mice. J Neurosci 38:1061-1072
Gregg, Brigid E; Botezatu, Nathalie; Brill, Joshua D et al. (2018) Gestational exposure to metformin programs improved glucose tolerance and insulin secretion in adult male mouse offspring. Sci Rep 8:5745
Semple, Erin; Hill, Jennifer W (2018) Sim1 Neurons Are Sufficient for MC4R-Mediated Sexual Function in Male Mice. Endocrinology 159:439-449
Ward, Kristen M; Yeoman, Larisa; McHugh, Cora et al. (2018) Atypical Antipsychotic Exposure May Not Differentiate Metabolic Phenotypes of Patients with Schizophrenia. Pharmacotherapy 38:638-650
Khan, Sabbir; Kowluru, Anjaneyulu (2018) CD36 mediates lipid accumulation in pancreatic beta cells under the duress of glucolipotoxic conditions: Novel roles of lysine deacetylases. Biochem Biophys Res Commun 495:2221-2226

Showing the most recent 10 out of 1823 publications