Metal chelation reduces skin epithelial inflammation and rescues epithelial cells from toxicity due to thermal injury in a rat model

Author:

El Ayadi Amina1ORCID,Wang Cheng Z2,Zhang Min2,Wetzel Michael1,Prasai Anesh1,Finnerty Celeste C1,Enkhbaatar Perenlei3,Herndon David N1,Ansari Naseem H2

Affiliation:

1. Department of Surgery, University of Texas Medical Branch, Galveston, TX 77555, USA

2. Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA

3. Department of Anesthesiology, 301 University Blvd., University of Texas Medical Branch, Galveston, TX 77555, USA

Abstract

Abstract Background One of the most pervasive complications of burn injury is wound progression, characterized by continuous tissue destruction in untreated wounds, which leads to wound infection, inflammation, oxidative stress and excessive scar formation. We determined whether additional tissue destruction could be attenuated with Livionex formulation (LF) lotion, which contains a metal-chelating agent and reduces inflammation in burn wounds. Methods We subjected male Sprague Dawley rats to a 2% total body surface area (TBSA) burn using a brass comb model and topically applied LF lotion (containing ethylenediaminetetraacetic acid and methyl sulfonyl methane) to the affected area every 8 hours over 3 days. Inflammatory cytokine levels, cell apoptosis and wound healing were compared in LF lotion-treated and untreated rats. Statistical analysis was performed using a one-way analysis of variance in conjunction with Tukey’s post-hoc test. Results Serum inflammatory cytokines were not detectable after 3 days, suggesting that small burn wounds induce only an immediate, localized inflammatory response. Microscopy revealed that LF lotion improved burn site pathology. Deoxynucleotidyl transferase biotin-d-UTP nick-end labeling staining showed reduced cell death in the LF-treated samples. LF lotion prevented the spread of tissue damage, as seen by increased amounts of Ki-67-positive nuclei in the adjacent epidermis and hair follicles. Tumor necrosis factor-alpha, interleukin-6 and inducible nitric oxide synthase levels in LF-treated skin sections from burned rats were comparable to the levels observed in unburned control sections, indicating that LF lotion reduces inflammation in and around the burn site. Conclusions These results establish LF lotion as a therapeutic agent for reducing inflammatory stress, cell death and tissue destruction when applied immediately after a burn injury. Further studies of LF lotion on large TBSA burns will determine its efficacy as an emergency treatment for reducing long-term morbidity and scarring.

Funder

National Institute of Environmental Health Sciences

National Institute of General Medical Sciences

Shriners Hospitals for Children

Army, Navy, NIH, Air Force, VA and Health Affairs

Publisher

Oxford University Press (OUP)

Subject

Critical Care and Intensive Care Medicine,Dermatology,Biomedical Engineering,Emergency Medicine,Immunology and Allergy,Surgery

Reference54 articles.

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2. Burn wound infections;Church;Clin Microbiol Rev.,2006

3. The treatment of burns: an exercise in emergency surgery;Jackson;Ann R Coll Surg Engl.,1953

4. Diagnosis in the management of burns;Jackson;Br Med J.,1959

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