2010
DOI: 10.3389/fphar.2010.00140
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Capsaicinoids, Chloropicrin and Sulfur Mustard: Possibilities for Exposure Biomarkers

Abstract: Incapacitating and irritating agents produce temporary disability persisting for hours to days after the exposure. One can be exposed to these agents occupationally in industrial or other working environments. Also general public can be exposed in special circumstances, like industrial accidents or riots. Incapacitating and irritating agents discussed in this review are chloropicrin and capsaicinoids. In addition, we include sulfur mustard, which is an old chemical warfare agent and known to cause severe long-… Show more

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Cited by 20 publications
(14 citation statements)
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References 129 publications
(193 reference statements)
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“…chlorine) (Gaskin et al, ); (3) vesicating agents (e.g. sulfur mustard) (Pesonen et al, ); and (4) organophosphorous compounds (i.e. nerve agents) (Pereira et al, ).…”
Section: Introductionmentioning
confidence: 99%
“…chlorine) (Gaskin et al, ); (3) vesicating agents (e.g. sulfur mustard) (Pesonen et al, ); and (4) organophosphorous compounds (i.e. nerve agents) (Pereira et al, ).…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, in view of the hypothesis of SM accumulation in adipose depots (Kehe et al 2008;Pesonen et al 2010;Somani and Babu 1989) mentioned in several reports but no animal experimental evidences to support this assumption, experiments on the tissue distribution of SM in rats after percutaneous exposure at three doses were performed. The distribution and the toxicokinetic behavior of intact SM in adipose tissues were initially investigated.…”
Section: Introductionmentioning
confidence: 99%
“…[114][115][116] Despite the different mode-of-action of SMs (hydrolysis and conjugation to glutathione involving β-lyase and S-oxidation) many studies indicate that DNA alkylation is related to its toxicity. 117 The alkylation pathway of both mustards follow a similar mechanism through a three-membered heterocycle and preferentially modifying the N7 position of guanine in DNA, comparable to the natural products leinamycin and azinomycin discussed in the previous section. In a first step the aziridium or episulfonium is attacked by a guanine residue.…”
Section: Artificial Chemical Agents Acting On Nucleobasesmentioning
confidence: 85%