Sarin effects

Moreover organophosphoric acid esters have found application as insecticides (e.g. Parathion). Some derivatives are highly toxic to man (e.g. Sarin, Soman). The organophosphonates act as inhibitors of the enzyme cholinesterase by phosphorylating it. This enzyme is involved in the proper function of the parasympathetic nervous system. A concentration of 5 x 10 g/L in the air can already cause strong toxic effects to man. 

Sarin SK, Sood A, Kumar M, Arora A, Amrapurkar D, Sharma BC, Konar A, Chawla YK, Jain RK, Nanda V, Kumar A, Hissar S, Lavate P, Lahoti D (2007) Effect of lowering HBV DNA levels by initial antiviral therapy before adding immunomodulator on treatment of chronic hepatitis B. Am J Gastroenterol 102 96-104... 

Burchfield, J.L, Duffy, F.H., and Sim, V.N. (1976). Persistent effect of sarin and dieldrin upon the primate electroencephalogram. Toxicology and Applied Pharmacology 35, 365-379. 

Sanchez F, Rodriguez-Alavarez MJ (1999) Effect of pH, conductivity and sediment size on thorium and radium activities along Jucar River (Spain). J Radioanal Nucl Chem 242 671-681 Sarin MM, Krishnaswami S, Somayajulu BLK, Moore WS (1990) Chemistry of U, Th, and Ra isotopes in the Ganga-Brahmaputra river system Weathering processes and fluxes to the bay of Bengal. Geochim Cosmochim Acta 54 1387-1396... 

Most chemical agents are essentially cumulative in their effects. The reason is that the human body detoxifies them very slowly or not at all. For example, a 1-h exposure to HD or CG followed within a few hours by another 1-h exposure has about the same effect as a single 2-h exposure. Continued exposure to low concentrations of HD may cause sensitivity to very low concentrations of HD. Other chemical agents also have cumulative effects. For example, an initial exposure to a small (less than lethal) amount of Sarin (GB) would decrease cholinesterase levels a second quantity less than the FDS0... 

Final Recommendations for Protecting Human Health From Potential Adverse Effects of Exposure to Agents GA (Tabun), GB (Sarin), and VX." Federal Register 68, No. 196 (October 9, 2003) 58348-58351. 

The toxic effects model translates the exposure profiles into casualty probabilities for the personnel, assuming a probabilistic dose-effect relationship. The casualty levels and spectra can be obtained for various type of health effects, e.g. eye effects, inhalation, percutane, subdivided in two levels (incapacitating and lethal), and various protection levels, e.g. no protection, suit only, mask only, mask and suit, and collective protection. Table 1 gives a typical result for one scenario. In case no protection is used, 63% of the population dies due to inhalation of sarin and 25% dies due to percutaneous exposure. Clearly, when both mask and suit are worn, the casualty levels are dropping drastically. 

High therapeutic effect was received with the usage of atropine (10 mg/kg, i.m.) and carboxime (30 mg/kg, i.m.) in animals poisoned with sarin, soman and VX. 

In contrast to dipiroxime, alloxime in therapeutic doses demonstrates a pronounced therapeutic effect in poisonings induced both by sarin and soman (rats and dogs) and by high toxic carbamates (carbofuran, ellocron, pirimor). 

Highly effective warfare agents (e.g. soman, sarin, tabun) and certain of their direct precursors. 

The use of a lipophilic zinc(II) macrocycle complex, 1-hexadecyl-1,4,7,10-tetraazacyclododecane, to catalyze hydrolysis of lipophilic esters, both phosphate and carboxy (425), links this Section to the previous Section. Here, and in studies of the catalysis of hydrolysis of 4-nitrophenyl acetate by the Zn2+ and Co2+ complexes of tris(4,5-di-n-propyl-2 -imidazolyl)phosphine (426) and of a phosphate triester, a phos-phonate diester, and O-isopropyl methylfluorophosphonate (Sarin) by [Cu(A(A(A/,-trimethyl-A/,-tetradecylethylenediamine)l (427), various micellar effects have been brought into play. Catalysis of carboxylic ester hydrolysis is more effectively catalyzed by A"-methylimidazole-functionalized gold nanoparticles than by micellar catalysis (428). Other reports on mechanisms of metal-assisted carboxy ester hydrolyses deal with copper(II) (429), zinc(II) (430,431), and palladium(II) (432). 

Nerve Agent Antidote Kit (NAAK or MARK I) consists of an atropine auto-injector (2 mg), a pralidoxime chloride auto-injector (2-Pam-Cl, 600 mg), the plastic clip joining the two injectors, and a foam case. The kit serve as a countermeasure to nerve agents, including tabun (GA), sarin (GB), soman (GD), GF, and VX. Military personnel can receive three MARK I for self/buddy aid. Possible side effects of atropine and/or 2-PAM-C1 are deemed insignificant in a nerve agent casualty. Intravenous atropine and 2-PAM-C1 can also be made available. The MARK I kit is manufactured by Survival Technology, Inc., Rockville, Maryland. 

While nerve agents vary in molecular structure, they all exert the same physiological effect on the body an increase in acetylcholine throughout the body caused by interference with a vital enzyme known as cholinesterase. The four primary nerve agents are tabun, sarin, soman, and VX. 

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