3.9 Article

Topical nitrogen mustard exposure causes systemic toxic effects in mice

Journal

EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY
Volume 67, Issue 2, Pages 161-170

Publisher

ELSEVIER GMBH, URBAN & FISCHER VERLAG
DOI: 10.1016/j.etp.2014.11.006

Keywords

Nitrogen mustard; Skin topical exposure; Systemic toxicity; Leucocytes; SKH-1 hairless mice

Funding

  1. Countermeasures Against Chemical Threats (CounterACT) Program, Office of the Director National Institutes of Health (OD)
  2. National Institute of Environmental Health Sciences (NIEHS) [U54ES015678]
  3. NIH
  4. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [U54ES015678] Funding Source: NIH RePORTER

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Vesicating agents sulfur mustard (SM) and nitrogen mustard (NM) are reported to be easily absorbed by skin upon exposure causing severe cutaneous injury and blistering. Our studies show that topical exposure of NM (3.2 mg) onto SKH-1 hairless mouse skin, not only caused skin injury, but also led to significant body weight loss and 40-80% mortality (120 h post-exposure), suggesting its systemic effects. Accordingly, further studies herein show that NM exposure initiated an increase in circulating white blood cells by 24 h (neutrophils, eosinophils and basophils) and thereafter a decrease (neutrophils, lymphocytes and monocytes). NM exposure also reduced both white and red pulp areas of the spleen. In the small intestine, NM exposure caused loss of membrane integrity of the surface epithelium, abnormal structure of glands and degeneration of villi. NM exposure also resulted in the dilation of glomerular capillaries of kidneys, and an increase in blood urea nitrogen/creatinine ratio. Our results here with NM are consistent with earlier reports that exposure to higher SM levels can cause damage to the hematopoietic system, and kidney, spleen and gastrointestinal tract toxicity. These outcomes will add to our understanding of the toxic effects of topical vesicant exposure, which might be helpful towards developing effective countermeasures against injuries from acute topical exposures. (C) 2014 Elsevier GmbH. All rights reserved.

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