| Literature DB >> 24801489 |
Brian M Keyser1, Devon K Andres1, Wesley W Holmes2, Danielle Paradiso2, Ashley Appell1, Valerie A Letukas1, Betty Benton1, Offie E Clark1, Xiugong Gao3, Prabhati Ray3, Dana R Anderson2, Radharaman Ray4.
Abstract
Mustard gas (sulfur mustard [SM], bis-[2-chloroethyl] sulfide) is a vesicating chemical warfare agent and a potential chemical terrorism agent. Exposure of SM causes debilitating skin blisters (vesication) and injury to the eyes and the respiratory tract; of these, the respiratory injury, if severe, may even be fatal. Therefore, developing an effective therapeutic strategy to protect against SM-induced respiratory injury is an urgent priority of not only the US military but also the civilian antiterrorism agencies, for example, the Homeland Security. Toward developing a respiratory medical countermeasure for SM, four different classes of therapeutic compounds have been evaluated in the past: anti-inflammatory compounds, antioxidants, protease inhibitors and antiapoptotic compounds. This review examines all of these different options; however, it suggests that preventing cell death by inhibiting apoptosis seems to be a compelling strategy but possibly dependent on adjunct therapies using the other drugs, that is, anti-inflammatory, antioxidant, and protease inhibitor compounds.Entities:
Keywords: anti-inflammatory; antioxidants; apoptosis; inhalation; protease; sulfur mustard
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Year: 2014 PMID: 24801489 DOI: 10.1177/1091581814532959
Source DB: PubMed Journal: Int J Toxicol ISSN: 1091-5818 Impact factor: 2.032