The goal of the Bio-Analytical Redox Biology (BARB) core is to provide state-of-the-art services in mitochondrial and cellular metabolism and oxidative stress assessment. Since its intiation in 2008, the BARB Core has provided services at a rate that has increased on average by 215% per year. New services will include the ex vivo measurement of cellular/tissue bioenergetics, mitochondrial metabolomics (citric acid cycle intermediates), and introduction of new measures of oxidative stress that will utilize 2-hydroxyethidium and related molecules employing mass spectrometry. These services will expand upon the current services and provide novel measures for research in diabetes and cardiometabolic disease.
The specific aims are: 1) Provide services to DRC Members and pilot &feasibility grant awardees in: (A) Mitochondrial metabolism: isolation, bioenergetics, membrane potential, ATP generation, oxidant production (amplex red), mt DNA damage;(B) Oxidative stress assessment (oxidized lipids, 3NT, aconitase inactivation, lipid peroxidation, LPO products, isoprostanes, GSH/GSSG, dihydroethidine and related compounds inactivation, S0D2 activity and GSH/GSSG);and (C) Cellular metabolism analyses - cell and tissue (permeabilized tissue - in situ/ex vivo) bioenergetics, citric acid cycle intermediate metabolomics and enzyme peptidomics. 2) To reduce cost and investigator time commitment by accessing the centralized resources of the core. 3) To provide investigators opportunities to learn and develop new research methodologies through recurring workshops and consultations that utilize BARB core services. 4) Development of new methodologies that extend research capabilities in redox and free radical biology.
These aims are based on the expressed needs of funded DRC investigators. The BARB core is unique within UAB and at NIDDK diabetes centers. The Core plans to continue the development of technologies to keep our investigators appraised of current developments in bioenergetics, metabolism, and oxidant stress quantification, via a continued outreach program consisting of tutorials and seminars.

Public Health Relevance

The BARB Core is at the forefront of methods assessing mitochondrial metabolism, energetics, and oxidative stress, which are processes central to the pathogenesis of diabetes and cardiometabolic disease. The constellation of core services reflects an area of excellence in the DRC investigator base, and is unique among NIDDK diabetes centers and nation-wide. The Core will continue its outstanding and increasing record of service and facilitate advances pertaining to metabolic and vascular patholoav in diabetes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK079626-06
Application #
8443899
Study Section
Special Emphasis Panel (ZDK1-GRB-S (O2))
Project Start
Project End
Budget Start
2013-03-25
Budget End
2014-02-28
Support Year
6
Fiscal Year
2013
Total Cost
$251,070
Indirect Cost
$63,821
Name
University of Alabama Birmingham
Department
Type
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Loomis, Stephanie J; Li, Man; Maruthur, Nisa M et al. (2018) Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results From the Atherosclerosis Risk in Communities Study. Diabetes 67:1684-1696
Wingo, Brooks C; Barry, Valene Garr; Ellis, Amy C et al. (2018) Comparison of segmental body composition estimated by bioelectrical impedance analysis and dual-energy X-ray absorptiometry. Clin Nutr ESPEN 28:141-147
Frugé, Andrew D; Cases, Mallory G; Howell, Carrie R et al. (2018) Fingernail and toenail clippings as a non-invasive measure of chronic cortisol levels in adult cancer survivors. Cancer Causes Control 29:185-191
Kim, Teayoun; Holleman, Cassie L; Nason, Shelly et al. (2018) Hepatic Glucagon Receptor Signaling Enhances Insulin-Stimulated Glucose Disposal in Rodents. Diabetes 67:2157-2166
Kreisler, A D; Mattock, M; Zorrilla, E P (2018) The duration of intermittent access to preferred sucrose-rich food affects binge-like intake, fat accumulation, and fasting glucose in male rats. Appetite 130:59-69
Sweatt, S Katherine; Gower, Barbara A; Chieh, Angela Y et al. (2018) Sleep quality is differentially related to adiposity in adults. Psychoneuroendocrinology 98:46-51
Chusyd, Daniella E; Brown, Janine L; Hambly, Catherine et al. (2018) Adiposity and Reproductive Cycling Status in Zoo African Elephants. Obesity (Silver Spring) 26:103-110
Ellis, Amy C; Hunter, Gary R; Goss, Amy M et al. (2018) Oral Supplementation with Beta-Hydroxy-Beta-Methylbutyrate, Arginine, and Glutamine Improves Lean Body Mass in Healthy Older Adults. J Diet Suppl :1-13
Bush, Nikki C; Resuehr, Holly E S; Goree, Laura Lee et al. (2018) A High-Fat Compared with a High-Carbohydrate Breakfast Enhances 24-Hour Fat Oxidation in Older Adults. J Nutr 148:220-226
Gupta, Rajesh; Nguyen, Dan C; Schaid, Michael D et al. (2018) Complement 1q-like-3 protein inhibits insulin secretion from pancreatic ?-cells via the cell adhesion G protein-coupled receptor BAI3. J Biol Chem 293:18086-18098

Showing the most recent 10 out of 643 publications