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Institution

Shriners Hospitals for Children - Galveston

HealthcareGalveston, Texas, United States
About: Shriners Hospitals for Children - Galveston is a healthcare organization based out in Galveston, Texas, United States. It is known for research contribution in the topics: Burn injury & Lean body mass. The organization has 249 authors who have published 420 publications receiving 15311 citations.


Papers
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Journal ArticleDOI
TL;DR: Following severe burn, a shift occurs toward a predominant Th2 phenotype, and exogenous IGF-I/IGFBP-3 treatment partially reverses this response.

24 citations

Journal ArticleDOI
TL;DR: It is proposed that PBMCs in critical illness upregulate their intracellular hemoglobin levels by a defense mechanism protecting the cell against cytotoxic concentrations of H2S and other gaseous transmitters, oxidants and free radicals produced in critically ill patients.
Abstract: The classical role of hemoglobin in the erythrocytes is to carry oxygen from the lungs to the tissues via the circulation However, hemoglobin also acts as a redox regulator and as a scavenger of the gaseous mediators nitric oxide (NO) and hydrogen sulfide (H2S) Here we show that upregulation of hemoglobin (α, β and δ variants of globin proteins) occurs in human peripheral blood mononuclear cells (PBMCs) in critical illness (patients with severe third-degree burn injury and patients with sepsis) The increase in intracellular hemoglobin concentration is a result of a combination of enhanced protein expression and uptake from the extracellular space via a CD163-dependent mechanism Intracellular hemoglobin preferentially localizes to the mitochondria, where it interacts with complex I and, on the one hand, increases mitochondrial respiratory rate and mitochondrial membrane potential, and on the other hand, protects from H2O2-induced cytotoxicity and mitochondrial DNA damage Both burn injury and sepsis were associated with increased plasma levels of H2S Incubation of mononuclear cells with H2S induced hemoglobin mRNA upregulation in PBMCs in vitro Intracellular hemoglobin upregulation conferred a protective effect against cell dysfunction elicited by H2S Hemoglobin uptake also was associated with a protection from, and induced the upregulation of, HIF-1α and Nrf2 mRNA In conclusion, PBMCs in critical illness upregulate their intracellular hemoglobin levels by a combination of active synthesis and uptake from the extracellular medium We propose that this process serves as a defense mechanism protecting the cell against cytotoxic concentrations of H2S and other gaseous transmitters, oxidants and free radicals produced in critically ill patients

24 citations

Journal ArticleDOI
01 Feb 2009-Burns
TL;DR: In this article, the duration of insulin resistance following recovery from the acute burn injury was measured with a standard 2-h oral glucose tolerance test in 46 severely burned children at 6, 9 or 12 months following initial injury.

24 citations

01 Aug 2016
TL;DR: In this article, the authors hypothesized that hypermetabolism contributes to muscle wasting in burn patients and hypothesized that oxidative enzymes are involved in the muscle wasting, but their hypothesis was not validated.
Abstract: Burn trauma results in prolonged hypermetabolism and skeletal muscle wasting. How hypermetabolism contributes to muscle wasting in burn patients remains unknown. We hypothesized that oxidative stre...

24 citations

Journal ArticleDOI
TL;DR: It is suggested that ONOO(-) plays a crucial role in the pathogenesis of pulmonary microvascular hyperpermeability and pulmonary dysfunction following burn and smoke inhalation injury in sheep.
Abstract: During acute lung injury, nitric oxide (NO) exerts cytotoxic effects by reacting with superoxide radicals, yielding the reactive nitrogen species peroxynitrite (ONOO−). ONOO− exerts cytotoxic effec...

23 citations


Authors

Showing all 250 results

NameH-indexPapersCitations
Robert R. Wolfe12456654000
Csaba Szabó12395861791
David N. Herndon108122754888
Steven E. Wolf7441921329
Blake B. Rasmussen6515218951
Marc G. Jeschke6417413903
Daniel L. Traber6262914801
Nicole S. Gibran6027314304
Donald S. Prough5850811644
David L. Chinkes5615111871
Labros S. Sidossis5322411636
Robert E. Barrow511307114
Ashok K. Chopra491997568
James A. Carson491577554
Celeste C. Finnerty4817210647
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20221
20215
202026
201928
201822
201746