Literature DB >> 24091052

Limitations and challenges in treatment of acute chemical warfare agent poisoning.

Horst Thiermann1, Franz Worek, Kai Kehe.   

Abstract

Recent news from Syria on a possible use of chemical warfare agents made the headlines. Furthermore, the motivation of terrorists to cause maximal harm shifts these agents into the public focus. For incidents with mass casualties appropriate medical countermeasures must be available. At present, the most important threats arise from nerve agents and sulfur mustard. At first, self-protection and protection of medical units from contamination is of utmost importance. Volatile nerve agent exposure, e.g. sarin, results in fast development of cholinergic crisis. Immediate clinical diagnosis can be confirmed on-site by assessment of acetylcholinesterase activity. Treatment with autoinjectors that are filled with 2mg atropine and an oxime (at present obidoxime, pralidoxime, TMB-4 or HI-6) are not effective against all nerve agents. A more aggressive atropinisation has to be considered and more effective oximes (if possible with a broad spectrum or a combination of different oximes) as well as alternative strategies to cope with high acetylcholine levels at synaptic sites should be developed. A further gap exists for the treatment of patients with sustained cholinergic crisis that has to be expected after exposure to persistent nerve agents, e.g. VX. The requirement for long-lasting artificial ventilation can be reduced with an oxime therapy that is optimized by using the cholinesterase status for guidance or by measures (e.g. scavengers) that are able to reduce the poison load substantially in the patients. For sulfur mustard poisoning no specific antidote is available until now. Symptomatic measures as used for treatment of burns are recommended together with surgical or laser debridement. Thus, huge amounts of resources are expected to be consumed as wound healing is impaired. Possible depots of sulfur mustard in tissues may aggravate the situation. More basic knowledge is necessary to improve substantially therapeutic options. The use of stem cells may provide a new and promising option.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Acetylcholinesterase; Chemical warfare agents; Human; Organophosphorus compounds; Sulfur mustard; Treatment

Mesh:

Substances:

Year:  2013        PMID: 24091052     DOI: 10.1016/j.cbi.2013.09.015

Source DB:  PubMed          Journal:  Chem Biol Interact        ISSN: 0009-2797            Impact factor:   5.192


  25 in total

1.  In vitro evaluation of the catalytic activity of paraoxonases and phosphotriesterases predicts the enzyme circulatory levels required for in vivo protection against organophosphate intoxications.

Authors:  Yacov Ashani; Haim Leader; Nidhi Aggarwal; Israel Silman; Franz Worek; Joel L Sussman; Moshe Goldsmith
Journal:  Chem Biol Interact       Date:  2016-05-06       Impact factor: 5.192

2.  Dynamic cytotoxic profiles of sulfur mustard in human dermal cells determined by multiparametric high-content analysis.

Authors:  Long Long; Wei Li; Wei Chen; Fei-Fei Li; Hua Li; Li-Li Wang
Journal:  Toxicol Res (Camb)       Date:  2016-01-11       Impact factor: 3.524

Review 3.  Mustard vesicating agent-induced toxicity in the skin tissue and silibinin as a potential countermeasure.

Authors:  Neera Tewari-Singh; Rajesh Agarwal
Journal:  Ann N Y Acad Sci       Date:  2016-06-21       Impact factor: 5.691

4.  Sulfur mustard induced mast cell degranulation in mouse skin is inhibited by a novel anti-inflammatory and anticholinergic bifunctional prodrug.

Authors:  Laurie B Joseph; Gabriella M Composto; Roberto M Perez; Hong-Duck Kim; Robert P Casillas; Ned D Heindel; Sherri C Young; Carl J Lacey; Jaya Saxena; Christophe D Guillon; Claire R Croutch; Jeffrey D Laskin; Diane E Heck
Journal:  Toxicol Lett       Date:  2017-11-07       Impact factor: 4.372

Review 5.  Acute and long-term consequences of exposure to organophosphate nerve agents in humans.

Authors:  Taiza H Figueiredo; James P Apland; Maria F M Braga; Ann M Marini
Journal:  Epilepsia       Date:  2018-08-29       Impact factor: 5.864

6.  Evaluating the broad-spectrum efficacy of the acetylcholinesterase oximes reactivators MMB4 DMS, HLö-7 DMS, and 2-PAM Cl against phorate oxon, sarin, and VX in the Hartley guinea pig.

Authors:  Christina M Wilhelm; Thomas H Snider; Michael C Babin; Gennady E Platoff; David A Jett; David T Yeung
Journal:  Neurotoxicology       Date:  2018-07-26       Impact factor: 4.294

7.  A comprehensive evaluation of the efficacy of leading oxime therapies in guinea pigs exposed to organophosphorus chemical warfare agents or pesticides.

Authors:  Christina M Wilhelm; Thomas H Snider; Michael C Babin; David A Jett; Gennady E Platoff; David T Yeung
Journal:  Toxicol Appl Pharmacol       Date:  2014-10-31       Impact factor: 4.219

Review 8.  Organophosphate-Hydrolyzing Enzymes as First-Line of Defence Against Nerve Agent-Poisoning: Perspectives and the Road Ahead.

Authors:  A R Satvik Iyengar; Abhay H Pande
Journal:  Protein J       Date:  2016-12       Impact factor: 2.371

9.  Detoxification of Organophosphate Poisoning Using Nanoparticle Bioscavengers.

Authors:  Zhiqing Pang; Che-Ming J Hu; Ronnie H Fang; Brian T Luk; Weiwei Gao; Fei Wang; Erdembileg Chuluun; Pavimol Angsantikul; Soracha Thamphiwatana; Weiyue Lu; Xinguo Jiang; Liangfang Zhang
Journal:  ACS Nano       Date:  2015-06-08       Impact factor: 15.881

10.  Kinetic analysis of oxime-assisted reactivation of human, Guinea pig, and rat acetylcholinesterase inhibited by the organophosphorus pesticide metabolite phorate oxon (PHO).

Authors:  Robert A Moyer; Kevin G McGarry; Michael C Babin; Gennady E Platoff; David A Jett; David T Yeung
Journal:  Pestic Biochem Physiol       Date:  2018-01-31       Impact factor: 3.963

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