Topically applied metal chelator reduces thermal injury progression in a rat model of brass comb burn

Burns. 2015 Dec;41(8):1775-1787. doi: 10.1016/j.burns.2015.08.012. Epub 2015 Sep 29.

Abstract

Oxidative stress may be involved in the cellular damage and tissue destruction as burn wounds continues to progress after abatement of the initial insult. Since iron and calcium ions play key roles in oxidative stress, this study tested whether topical application of Livionex formulation (LF) lotion, that contains disodium EDTA as a metal chelator and methyl sulfonyl methane (MSM) as a permeability enhancer, would prevent or reduce burns.

Methods: We used an established brass comb burn model with some modifications. Topical application of LF lotion was started 5 min post-burn, and repeated every 8 h for 3 consecutive days. Rats were euthanized and skin harvested for histochemistry and immunohistochemistry. Formation of protein adducts of 4-hydroxynonenal (HNE), malonadialdehyde (MDA) and acrolein (ACR) and expression of aldehyde dehydrogenase (ALDH) isozymes, ALDH1 and ALDH2 were assessed.

Results: LF lotion-treated burn sites and interspaces showed mild morphological improvement compared to untreated burn sites. Furthermore, the lotion significantly decreased the immunostaining of lipid aldehyde-protein adducts including protein -HNE, -MDA and -ACR adducts, and restored the expression of aldehyde dehydrogenase isozymes in the unburned interspaces.

Conclusion: This data, for the first time, demonstrates that a topically applied EDTA-containing lotion protects burns progression with a concomitant decrease in the accumulation of reactive lipid aldehydes and protection of aldehyde dehydrogenase isozymes. Present studies are suggestive of therapeutic intervention of burns by this novel lotion.

Keywords: Brass comb burn; Burn progression; Iron chelation; Oxidative stress; Reactive aldehydes; Thermal injury; Wound healing.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acrolein / metabolism
  • Administration, Cutaneous
  • Aldehyde Dehydrogenase / drug effects
  • Aldehyde Dehydrogenase / metabolism
  • Aldehyde Dehydrogenase 1 Family
  • Aldehyde Dehydrogenase, Mitochondrial
  • Aldehydes / metabolism
  • Animals
  • Burns*
  • Chelating Agents / pharmacology*
  • Copper
  • Dimethyl Sulfoxide / pharmacology*
  • Disease Models, Animal
  • Edetic Acid / pharmacology*
  • Immunohistochemistry
  • Malondialdehyde / metabolism
  • Mitochondrial Proteins / drug effects
  • Mitochondrial Proteins / metabolism
  • Oxidative Stress / drug effects*
  • Permeability / drug effects
  • Rats
  • Retinal Dehydrogenase / drug effects
  • Retinal Dehydrogenase / metabolism
  • Skin / drug effects*
  • Skin / metabolism
  • Skin / pathology
  • Sulfones / pharmacology*
  • Trauma Severity Indices
  • Zinc

Substances

  • Aldehydes
  • Chelating Agents
  • Mitochondrial Proteins
  • Sulfones
  • brass
  • Malondialdehyde
  • Acrolein
  • Copper
  • Edetic Acid
  • dimethyl sulfone
  • Aldehyde Dehydrogenase 1 Family
  • Aldehyde Dehydrogenase
  • Aldehyde Dehydrogenase, Mitochondrial
  • Aldh2 protein, rat
  • Aldh1a1 protein, rat
  • Retinal Dehydrogenase
  • Zinc
  • 4-hydroxy-2-nonenal
  • Dimethyl Sulfoxide