Animal Phenotyping Core A thorough understanding of the processes controlling the response to nutrients and of the mechanisms that contribute to obesity and related metabolic diseases is required if we are to effectively combat these conditions. The detailed analysis of animals with altered metabolism (e.g. due to dietary, molecular, genetic, or pharmacological manipulation) at a level that reveals basic underlying mechanisms of control requires specialized expertise and technology not normally available to individual investigators. Established in 2006, the goals of the MNORC Animal Phenotyping Core was are to provide state-of-the art equipment, services and consultative advice regarding the detailed metabolic phenotyping of rodent models of metabolic diseases. The Animal Phenotyping Core makes the metabolic analysis of rodent models of disease available, expeditious, affordable, effective, and convenient for individual investigators. In addition to providing education, consultation and advice regarding the analysis of rat and mouse models with altered metabolism, the Core provides phenotyping services on specialized equipment that it operates. Specifically, the core determines body composition and utilizes the CLAMS apparatus and other systems to examine metabolic rate, respiratory quotient, food consumption, and activity in rodent models of metabolic disease. The Core also examines the response to exercise and examines cardiovascular and ether parameters by telemetry in rodents. The Core performs hyperinsulinemic/euglycemic clamp studies including specialized analysis of metabolite storage and release in rats and mice, as well as providing catheterization/cannulation services and tissue harvesting in rodents. Thus, overall, the Animal Phenotyping Core will consultatively aid individual investigators in designing an appropriate experimental plan for the metabolic analysis of animal models relevant to obesity and then provide the tools and services necessary to effect this analysis. This research is relevant to public health because it will increase our understanding of the events that underlie the development of obesity and its complications, and hence will facilitate the development of improved diagnostic, prevention and treatment strategies.

Public Health Relevance

Obesity has become a national problem that has defied easy treatment. The Animal Phenotyping Core of the Michigan Nutrition Obesity Research Center will provide investigators with advanced phenotyping techniques to understand the response to nutrition and/or other mechanisms that underlie obesity and alterations in metabolism in rodent models of disease. These insights will enable the design of novel dietary, exercise and medication interventions to control obesity and obesity-related diseases

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK089503-04
Application #
8490370
Study Section
Special Emphasis Panel (ZDK1-GRB-2)
Project Start
Project End
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
4
Fiscal Year
2013
Total Cost
$44,992
Indirect Cost
$16,058
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Zhang, Kezhong; Kim, Hyunbae; Fu, Zhiyao et al. (2018) Deficiency of the Mitochondrial NAD Kinase Causes Stress-Induced Hepatic Steatosis in Mice. Gastroenterology 154:224-237
Dinov, Ivo D; Palanimalai, Selvam; Khare, Ashwini et al. (2018) Randomization-Based Statistical Inference: A Resampling and Simulation Infrastructure. Teach Stat 40:64-73
Isaman, Deanna J M; Rothberg, Amy E (2018) Weight Mobility and Obesity in a Representative Sample of the US Adult Population. Int J Endocrinol 2018:4561213
Wernisch, Stefanie; Afshinnia, Farsad; Rajendiran, Thekkelnaycke et al. (2018) Probing the application range and selectivity of a differential mobility spectrometry-mass spectrometry platform for metabolomics. Anal Bioanal Chem 410:2865-2877
Assari, Shervin (2018) Self-rated Health and Mortality due to Kidney Diseases: Racial Differences in the United States. Adv Biomed Res 7:4
Li, Ziru; Hardij, Julie; Bagchi, Devika P et al. (2018) Development, regulation, metabolism and function of bone marrow adipose tissues. Bone 110:134-140
Wilson, Matthew J; Sen, Ananda; Bridges, Dave et al. (2018) Higher baseline expression of the PTGS2 gene and greater decreases in total colonic fatty acid content predict greater decreases in colonic prostaglandin-E2 concentrations after dietary supplementation with ?-3 fatty acids. Prostaglandins Leukot Essent Fatty Acids 139:14-19
Ryan, Benjamin J; Van Pelt, Douglas W; Guth, Lisa M et al. (2018) Plasma ferritin concentration is positively associated with in vivo fatty acid mobilization and insulin resistance in obese women. Exp Physiol 103:1443-1447
Kalinin, Alexandr A; Allyn-Feuer, Ari; Ade, Alex et al. (2018) 3D Shape Modeling for Cell Nuclear Morphological Analysis and Classification. Sci Rep 8:13658
Harvey, Innocence; Stephenson, Erin J; Redd, JeAnna R et al. (2018) Glucocorticoid-Induced Metabolic Disturbances Are Exacerbated in Obese Male Mice. Endocrinology 159:2275-2287

Showing the most recent 10 out of 342 publications