(Swine Core) The central function of the Indiana Diabetes Research Center (IDRC) Swine Core (a Regional/Shared Resource Core) is to reduce barriers to the use of Ossabaw swine, a unique animal model that closely approximates human metabolic syndrome (MetS) and progression to type 2 diabetes. Providing this animal resource enables testing of numerous hypotheses about the integrated, in vivo pathogenesis and long-term complications of MetS and type 2 diabetes and provides tissues for studies of cellular and molecular mechanisms. The Comparative Medicine Center, a collaboration between Purdue University and Indiana University School of Medicine (lUSM), has the only research and large-scale breeding colony of Ossabaw miniature swine in the world. Induced by an excess calorie atherogenic diet, Ossabaw swine develop MetS and atherosclerosis among other complications, and are an ideal model for testing human therapies. The Ossabaw swine resource has been used for numerous studies, including metabolism in skeletal muscle and liver, percutaneous catheter interventions and stents, lithotripsy of kidney stones, and bariatric surgery among others. The current and projected demand for Ossabaw miniature swine for NIDDK and several NIH Institutes, universities and biomedical and biotechnology companies clearly states the need for this animal model and justifies this Core as a Regional/National Shared Resource. The Swine Core is a critical interface in the translation of research from simpler animal models (Rodent Core) to humans (Translation Core). Islet and Microscopy Cores will be complementary with the Swine Core for basic cellular characterization. The primary aims of the Swine Core are to (1) provide quality control and care of the breeding colony of Ossabaw swine, (2) provide quality control of diet-induced MetS and diabetes (MetS/D), (3) phenotype the endocrine, metabolic, and dyslipidemia indices of MetS/D, (4) phenotype cardiovascular disease, and (5) provide a tissue and data bank for distribution for research studies.
These aims of the Swine Core will reduce barriers to study of this highly relevant animal model, and will facilitate the progressive translation of research from simpler, less complex models 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 #
5P30DK097512-05
Application #
9772441
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
5
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Type
DUNS #
603007902
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Mulukutla, Surya N; Tersey, Sarah A; Hampe, Christiane S et al. (2018) Elevated unmethylated and methylated insulin DNA are unique markers of A+?+ ketosis prone diabetes. J Diabetes Complications 32:193-195
González, Frank; Considine, Robert V; Abdelhadi, Ola A et al. (2018) Saturated fat ingestion promotes lipopolysaccharide-mediated inflammation and insulin resistance in PCOS. J Clin Endocrinol Metab :
Hood, Sula; Irby-Shasanmi, Amy; de Groot, Mary et al. (2018) Understanding Diabetes-Related Distress Characteristics and Psychosocial Support Preferences of Urban African American Adults Living With Type 2 Diabetes: A Mixed-Methods Study. Diabetes Educ 44:144-157
Engle, Staci E; Antonellis, Patrick J; Whitehouse, Logan S et al. (2018) A CreER mouse to study melanin concentrating hormone signaling in the developing brain. Genesis 56:e23217
Fritz, Brandon M; Muñoz, Braulio; Yin, Fuqin et al. (2018) A High-fat, High-sugar 'Western' Diet Alters Dorsal Striatal Glutamate, Opioid, and Dopamine Transmission in Mice. Neuroscience 372:1-15
Marasco, Michelle R; Conteh, Abass M; Reissaus, Christopher A et al. (2018) Interleukin-6 Reduces ?-Cell Oxidative Stress by Linking Autophagy With the Antioxidant Response. Diabetes 67:1576-1588
Sims, Emily K; Park, Grace; Mather, Kieren J et al. (2018) Immune reconstitution in ART treated, but not untreated HIV infection, is associated with abnormal beta cell function. PLoS One 13:e0197080
Beli, Eleni; Yan, Yuanqing; Moldovan, Leni et al. (2018) Restructuring of the Gut Microbiome by Intermittent Fasting Prevents Retinopathy and Prolongs Survival in db/db Mice. Diabetes 67:1867-1879
Chen, Melinda E; Chandramouli, Aaditya G; Considine, Robert V et al. (2018) Comparison of ?-Cell Function Between Overweight/Obese Adults and Adolescents Across the Spectrum of Glycemia. Diabetes Care 41:318-325
Aslamy, Arianne; Oh, Eunjin; Ahn, Miwon et al. (2018) Exocytosis Protein DOC2B as a Biomarker of Type 1 Diabetes. J Clin Endocrinol Metab 103:1966-1976

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