Literature DB >> 2730340

Survivors of soman poisoning: recovery of the soman LD50 to control value in the presence of extensive acetylcholinesterase inhibition.

J G Clement1.   

Abstract

Initially, mice were pretreated with atropine (17.4 mg/kg; IP) and the oxime reactivator HI-6 (50 mg/kg; IP) 5 min prior to an injection of soman (287 micrograms/kg, SC); approximately 2.1 x LD50 dose). More than 95% of the mice survived this dose of soman with atropine and HI-6 pretreatment. In these survivors of soman poisoning the return of the soman LD50 value to control value (124 micrograms/kg, SC) was determined at various times after the initial soman exposure. Mice which survived exposure to a lethal dose of soman by pretreatment with atropine and HI-6 were sensitized to the lethal effects of soman upon reexposure. The SC soman LD50 at 4 h, after surviving the initial soman exposure, was 20 micrograms/kg. The normal soman LD50 (as evidenced by a LD50 value which was not significantly different from the control value) returned within 4 days, at which time there was still extensive acetylcholinesterase inhibition in all brain regions (striatum, pons-medulla, cerebellum, hypothalamus, hippocampus), diaphragm and erythrocytes. Serum carboxylesterase recovered to control levels within 48 h, whereas liver carboxylesterase activity was not inhibited following the initial soman exposure. The results demonstrate that there is an excess of acetylcholinesterase which is required for normal response in the toxicological sense.

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Year:  1989        PMID: 2730340     DOI: 10.1007/bf00316438

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  15 in total

1.  Comparison of the effects of inhibition of external, internal and total acetylcholinesterase upon ganglionic transmission.

Authors:  R J McISAAC; G B KOELLE
Journal:  J Pharmacol Exp Ther       Date:  1959-05       Impact factor: 4.030

2.  [Relationship between cholinesterase activity and acetylcholine of the brains of mice acutely intoxicated with soman].

Authors:  X Zhang; B Y Qin
Journal:  Zhongguo Yao Li Xue Bao       Date:  1985-03

3.  Correlation between signs of toxicity and some biochemical changes in rats poisoned by soman.

Authors:  R C Jović
Journal:  Eur J Pharmacol       Date:  1974-02       Impact factor: 4.432

4.  De novo synthesis of acetylcholinesterase in guinea pig retina after inhibition by pinacolyl methylphosphonofluoridate.

Authors:  L W Harris; H I Yamamura; J H Fleisher
Journal:  Biochem Pharmacol       Date:  1971-10       Impact factor: 5.858

5.  The spontaneous recovery of respiration and neuromuscular transmission in the rat after anticholinesterase poisoning.

Authors:  E Meeter; O L Wolthuis
Journal:  Eur J Pharmacol       Date:  1968-03       Impact factor: 4.432

6.  Dealkylation studies on inhibited acetylcholinesterase.

Authors:  D B Coult; D J Marsh; G Read
Journal:  Biochem J       Date:  1966-03       Impact factor: 3.857

7.  Role of aliesterase in organophosphate poisoning.

Authors:  J G Clement
Journal:  Fundam Appl Toxicol       Date:  1984-04

8.  Toxicity of soman after repetitive injection of sublethal doses in guinea-pig and mouse.

Authors:  S H Sterri; S Lyngaas; F Fonnum
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1981-07

9.  The influence of 2-/o-cresyl/-4 H-1 : 3 : 2-benzodioxa-phosphorin-2-oxide (CBDP) on organophosphate poisoning and its therapy.

Authors:  B Bosković
Journal:  Arch Toxicol       Date:  1979-07-11       Impact factor: 5.153

10.  Relationship between inhibition of acetylcholinesterase and response of the rat phrenic nerve-diaphragm preparation to indirect stimulation at higher frequencies.

Authors:  P F Heffron; F Hobbiger
Journal:  Br J Pharmacol       Date:  1979-06       Impact factor: 8.739

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  2 in total

1.  Biological monitoring of exposure to nerve agents.

Authors:  J Bajgar
Journal:  Br J Ind Med       Date:  1992-09

2.  The functional role of molecular forms of acetylcholinesterase in neuromuscular transmission.

Authors:  R W Busker; J J Zijlstra; H J van der Wiel; H P van Helden
Journal:  Neurochem Res       Date:  1994-06       Impact factor: 3.996

  2 in total

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