application) The major goal of the Clinical Nutrition Research Unit (CNRU) at the University of Washington is to promote and enhance interdisciplinary nutrition research by bringing together basic science and clinical investigators on a cooperative basis. Because of the multidisciplinary nature of nutrition, close interaction across disciplines and optimal use of resources is necessary to better understand the relationships among diet, health and disease states. By providing a number of Core facilities, the CNRU integrates and coordinates health and disease states. By providing a number of Core facilities, the CNRU integrates and coordinates research activities in the field of nutrition and attempts to foster new interdisciplinary research collaboration, stimulate new research activities, improve nutrition education at multiple levels and facilitate the nutritional management of patients. The five Cores are: 1) a Laboratory Core to provide affiliate investigators with cost-efficient state-of-the-art nutritional assays and to help with new methods development; 2) a Clinical Research Core to provide facilities and help for investigators with their clinical research, and to provide a patient registry, behavioral psychologist, and biostatistical unit; 3) a Body Composition and Energy Expenditure Core to provide facilities for measuring body composition and energy expenditure; 4) a Nutrient-Gene Core to provide genetically-defined mouse models for use in studies of nutrient-gene interactions; and 5) an Administrative and Enrichment Core that is responsible for the day-to-day administration of the CNRU. This Core also arranges a series of seminars, retreats, and Visiting Professorships, and administers the Pilot and Feasibility and New Investigator Programs that are aimed at stimulating nutrition research by junior investigators and by more established investigators new to the field of nutrition in response to evolving research interests at the University of Washington. Thus, the CNRU provides facilities and support for the large and varied nutrition research base of the University in 6 major areas (lipids and atherosclerosis, diabetes, body weight regulation and obesity cancer, women?s health, and aging), thereby stimulating not only research, but also educational and clinical activities in the area of nutrition.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK035816-19
Application #
6693333
Study Section
Special Emphasis Panel (ZDK1-GRB-8 (M1))
Program Officer
Miles, Carolyn
Project Start
1985-09-01
Project End
2005-11-30
Budget Start
2003-12-01
Budget End
2004-11-30
Support Year
19
Fiscal Year
2004
Total Cost
$920,000
Indirect Cost
Name
University of Washington
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Du, Dan; Gu, Haiwei; Djukovic, Danijel et al. (2018) Multiplatform Metabolomics Investigation of Antiadipogenic Effects on 3T3-L1 Adipocytes by a Potent Diarylheptanoid. J Proteome Res 17:2092-2101
Vaisar, Tomáš; Couzens, Erica; Hwang, Arnold et al. (2018) Type 2 diabetes is associated with loss of HDL endothelium protective functions. PLoS One 13:e0192616
Anderson, Lindsey J; Tamayose, Jamie M; Garcia, Jose M (2018) Use of growth hormone, IGF-I, and insulin for anabolic purpose: Pharmacological basis, methods of detection, and adverse effects. Mol Cell Endocrinol 464:65-74
Han, Seung Jin; Boyko, Edward J; Kim, Soo Kyung et al. (2018) Association of Thigh Muscle Mass with Insulin Resistance and Incident Type 2 Diabetes Mellitus in Japanese Americans. Diabetes Metab J 42:488-495
Wander, Pandora L; Hayashi, Tomoshige; Sato, Kyoko Kogawa et al. (2018) Design and validation of a novel estimator of visceral adipose tissue area and comparison to existing adiposity surrogates. J Diabetes Complications 32:1062-1067
Bornfeldt, Karin E; Kramer, Farah; Batorsky, Anna et al. (2018) A Novel Type 2 Diabetes Mouse Model of Combined Diabetic Kidney Disease and Atherosclerosis. Am J Pathol 188:343-352
Haenisch, Michael; Treuting, Piper M; Brabb, Thea et al. (2018) Pharmacological inhibition of ALDH1A enzymes suppresses weight gain in a mouse model of diet-induced obesity. Obes Res Clin Pract 12:93-101
Bentsen, Marie Aare; Mirzadeh, Zaman; Schwartz, Michael W (2018) Revisiting How the Brain Senses Glucose-And Why. Cell Metab :
Faber, Chelsea L; Matsen, Miles E; Velasco, Kevin R et al. (2018) Distinct Neuronal Projections From the Hypothalamic Ventromedial Nucleus Mediate Glycemic and Behavioral Effects. Diabetes 67:2518-2529
Goh, Charlene E; Mooney, Stephen J; Siscovick, David S et al. (2018) Medical facilities in the neighborhood and incidence of sudden cardiac arrest. Resuscitation 130:118-123

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