This application seeks continued funding for our multidisciplinary Burn Trauma Center which began in 1974. The Center has continued to evolve to keep pace with the exciting new knowledge in biology and the state-of-the- art methods for conduct of clinical investigations and mechanistic studies in model systems. The Center's research addresses the underlying basis for metabolic events produced by life-threatening hypermetabolism and organ failure of severe burn injury. The unifying hypothesis is that burn injury uniquely changes the homeostasis of nitrogen and major energy-yielding substrate metabolism and profoundly reintegrates inter-organ cooperatively in nitrogen and energy economy. The net effect is a nitrogen catabolic state which compromises wound healing and recovery and currently, this state is refractory to treatment. This reintegration leads to a redistribution of amino acid, protein, and substrate metabolism among the wounded tissues and major organs by reordering carbon and nitrogen flow within and among body regions. To test the foregoing hypothesis, investigations are conducted in healthy volunteers and patients at the whole body level using non-invasive state-of-the-art clinical investigation tools. Human studies are necessary because the metabolic status of the burned patient represents more than a sum of the elements of metabolism studied in isolation. Mechanistic studies are also needed if rational and more effective metabolically designed substrate (nutritional) and pharmacological interventions are to be developed to improve patient care. Therefore, the defining feature of this Center is an exciting, integrated mixture of human and animal studies, in vivo and in vitro, observational, interventional, basic, and more applied studies with a major focus on interrelated aspects of specific amino acids, glucose, and fatty acid metabolism and the multiple signals involved. Thus, four projects are proposed: addressing (1) energy and nitrogen metabolism; (2) tissue-specific contributions to the altered metabolic state; (3) molecular mechanisms of burn-induced insulin resistance; and (4) molecular basis of hepatic hypermetabolism in burns. These synergistic studies will interact within and be supported by the Core facilities which provide technical, professional, and analytical services. These facilities include: (1) Clinical studies, (2) Animal studies, (3) Mass spectrometry, (4) Nuclear magnetic resonance spectroscopy, (5) Cyclotron and radiochemistry, and PET camera, (6) Computational and statistical consultation, and (7) Biochemical synthesis and image analysis.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center (P50)
Project #
5P50GM021700-26
Application #
6476330
Study Section
Special Emphasis Panel (ZGM1-TB-4 (01))
Program Officer
Somers, Scott D
Project Start
1977-12-01
Project End
2003-03-31
Budget Start
2001-12-01
Budget End
2003-03-31
Support Year
26
Fiscal Year
2002
Total Cost
$1,171,372
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02199
Tao, Rongya; Wang, Caixia; Stöhr, Oliver et al. (2018) Inactivating hepatic follistatin alleviates hyperglycemia. Nat Med 24:1058-1069
Nakazawa, Harumasa; Chang, Kyungho; Shinozaki, Shohei et al. (2017) iNOS as a Driver of Inflammation and Apoptosis in Mouse Skeletal Muscle after Burn Injury: Possible Involvement of Sirt1 S-Nitrosylation-Mediated Acetylation of p65 NF-?B and p53. PLoS One 12:e0170391
Frydman, Galit H; Marini, Robert P; Bakthavatchalu, Vasudevan et al. (2017) Local and Systemic Changes Associated with Long-term, Percutaneous, Static Implantation of Titanium Alloys in Rhesus Macaques (Macaca mulatta). Comp Med 67:165-175
Khan, Mohammed A S; Khan, Mohammed F; Kashiwagi, Shizuka et al. (2017) An ALPHA7 Nicotinic Acetylcholine Receptor Agonist (GTS-21) Promotes C2C12 Myonuclear Accretion in Association with Release of Interleukin-6 (IL-6) and Improves Survival in Burned Mice. Shock 48:227-235
Li, Peng; Tompkins, Ronald G; Xiao, Wenzhong et al. (2017) KERIS: kaleidoscope of gene responses to inflammation between species. Nucleic Acids Res 45:D908-D914
Kashiwagi, Shizuka; Khan, Mohammed A S; Yasuhara, Shingo et al. (2017) Prevention of Burn-Induced Inflammatory Responses and Muscle Wasting by GTS-21, a Specific Agonist for ?7 Nicotinic Acetylcholine Receptors. Shock 47:61-69
Agarwal, Shailesh; Loder, Shawn; Brownley, Cameron et al. (2016) Inhibition of Hif1? prevents both trauma-induced and genetic heterotopic ossification. Proc Natl Acad Sci U S A 113:E338-47
Shank, Erik S; Martyn, Jeevendra A; Donelan, Mathias B et al. (2016) Ultrasound-Guided Regional Anesthesia for Pediatric Burn Reconstructive Surgery: A Prospective Study. J Burn Care Res 37:e213-7
Copps, Kyle D; Hançer, Nancy J; Qiu, Wei et al. (2016) Serine 302 Phosphorylation of Mouse Insulin Receptor Substrate 1 (IRS1) Is Dispensable for Normal Insulin Signaling and Feedback Regulation by Hepatic S6 Kinase. J Biol Chem 291:8602-17
Law, Nathan C; White, Morris F; Hunzicker-Dunn, Mary E (2016) G protein-coupled receptors (GPCRs) That Signal via Protein Kinase A (PKA) Cross-talk at Insulin Receptor Substrate 1 (IRS1) to Activate the phosphatidylinositol 3-kinase (PI3K)/AKT Pathway. J Biol Chem 291:27160-27169

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