Literature DB >> 15147793

Biochemical changes in mouse lung after subcutaneous injection of the sulfur mustard 2-chloroethyl 4-chlorobutyl sulfide.

Nabil M Elsayed1, Stanley T Omaye.   

Abstract

Sulfur mustard (HD) is a vesicant-type chemical warfare agent (CWA) introduced in World War I which continues to be produced, stockpiled, and occasionally deployed by some countries, and could be used potentially by terrorists. Exposure to HD can cause erythema, blisters, corneal opacity, and airway damage. We have reported previously that subcutaneous (SC) injection of immunodeficient athymic nude mice with the half mustard butyl 2-chloroethyl sulfide (BCS) causes systemic biochemical changes in several organs distal to the exposure site. In the present study, we examined the response of non-immunodeficient Swiss Webster mice to the mustard, 2-chloroethyl 4-chlorobutyl sulfide (CECBS). In a pilot study, we found that a single SC injection of 20-25 microl/mouse causes death within 24h. Consequently, we used 5 microl/mouse (approx. 0.017 mg/kg body weight) of neat CECBS or an equal volume of saline as control. We examined the lungs after 1, 24, and 48 h for biochemical changes including total and oxidized glutathione, protein, DNA, and lipid peroxidation contents in tissue homogenate, and superoxide dismutase, catalase, glucose-6-phosphate dehydrogenase, and glutathione S-transferases activities in the cytosol. After 1h and/or 24h, we found statistically significant changes that were resolved by 48 h. These changes mimicked those of HD and BCS and were generally consistent with free radical-mediated oxidative stress. The implications of these observations are two-fold. First, dermal exposure to low-dose mustard gas could elicit systemic changes impacting distal organs such as the lungs. It also suggests that antioxidants could potentially modulate the response and reduce the damage. Second, although the use of known CWAs such as HD is prohibited, analogs that are not recognized as agents are as toxic and could be dangerous if acquired and used by potential terrorists.

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Year:  2004        PMID: 15147793     DOI: 10.1016/j.tox.2004.02.020

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  12 in total

1.  Role of reactive nitrogen species generated via inducible nitric oxide synthase in vesicant-induced lung injury, inflammation and altered lung functioning.

Authors:  Vasanthi R Sunil; Jianliang Shen; Kinal Patel-Vayas; Andrew J Gow; Jeffrey D Laskin; Debra L Laskin
Journal:  Toxicol Appl Pharmacol       Date:  2012-03-14       Impact factor: 4.219

2.  Role of MAP kinases in regulating expression of antioxidants and inflammatory mediators in mouse keratinocytes following exposure to the half mustard, 2-chloroethyl ethyl sulfide.

Authors:  Adrienne T Black; Laurie B Joseph; Robert P Casillas; Diane E Heck; Donald R Gerecke; Patrick J Sinko; Debra L Laskin; Jeffrey D Laskin
Journal:  Toxicol Appl Pharmacol       Date:  2010-04-09       Impact factor: 4.219

3.  Inhibition of NADPH cytochrome P450 reductase by the model sulfur mustard vesicant 2-chloroethyl ethyl sulfide is associated with increased production of reactive oxygen species.

Authors:  Joshua P Gray; Vladimir Mishin; Diane E Heck; Debra L Laskin; Jeffrey D Laskin
Journal:  Toxicol Appl Pharmacol       Date:  2010-06-02       Impact factor: 4.219

Review 4.  Sulfur mustard-induced pulmonary injury: therapeutic approaches to mitigating toxicity.

Authors:  Barry Weinberger; Jeffrey D Laskin; Vasanthi R Sunil; Patrick J Sinko; Diane E Heck; Debra L Laskin
Journal:  Pulm Pharmacol Ther       Date:  2010-09-17       Impact factor: 3.410

Review 5.  Oxidants and antioxidants in sulfur mustard-induced injury.

Authors:  Jeffrey D Laskin; Adrienne T Black; Yi-Hua Jan; Patrick J Sinko; Ned D Heindel; Vasanthi Sunil; Diane E Heck; Debra L Laskin
Journal:  Ann N Y Acad Sci       Date:  2010-08       Impact factor: 5.691

6.  Treatment with the catalytic metalloporphyrin AEOL 10150 reduces inflammation and oxidative stress due to inhalation of the sulfur mustard analog 2-chloroethyl ethyl sulfide.

Authors:  Heidi C O'Neill; Carl W White; Livia A Veress; Tara B Hendry-Hofer; Joan E Loader; Elysia Min; Jie Huang; Raymond C Rancourt; Brian J Day
Journal:  Free Radic Biol Med       Date:  2010-02-04       Impact factor: 7.376

7.  Glutathione and malondialdehyde levels in late pulmonary complications of sulfur mustard intoxication.

Authors:  Majid Shohrati; Mostafa Ghanei; Navvab Shamspour; Fatemeh Babaei; Majid Norozi Abadi; Mahvash Jafari; Ali Amini Harandi; Amini Harandi Ali
Journal:  Lung       Date:  2009-10-28       Impact factor: 2.584

8.  Protective effect of liposome-encapsulated glutathione in a human epidermal model exposed to a mustard gas analog.

Authors:  Victor Paromov; Sudha Kumari; Marianne Brannon; Naga S Kanaparthy; Hongsong Yang; Milton G Smith; William L Stone
Journal:  J Toxicol       Date:  2011-05-30

9.  Inhibition of inducible Nitric Oxide Synthase by a mustard gas analog in murine macrophages.

Authors:  Min Qui; Victor M Paromov; Hongsong Yang; Milton Smith; William L Stone
Journal:  BMC Cell Biol       Date:  2006-11-30       Impact factor: 4.241

10.  Sulfur mustard toxicity following dermal exposure: role of oxidative stress, and antioxidant therapy.

Authors:  Victor Paromov; Zacharias Suntres; Milton Smith; William L Stone
Journal:  J Burns Wounds       Date:  2007-10-30
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