Literature DB >> 7447543

comparison of the efficacy of HS-6 versus HI-6 when combined with atropine, pyridostigmine and clonazepam for soman poisoning in the monkey.

J Lipp, T Dola.   

Abstract

Monkeys were exposed to varying doses of soman and given therapy. Therapy consisted of pyridostigmine, clonazepam, atropine and HS-6 or HI-6. Cerebral electrical activity, heart rate, respiration, systemic blood pressure and cholinesterase activity were recorded thoughtout the experiment. The animals in the HS-6 series were divided into 4 groups depending upon the dose of soman; one group received 30 microgram/kg of soman, the second group received 40 microgran/kg. All animals in the HI06 series survived while only one of three monkeys in the fourth group survived. Administration of therapy immediately suppressed all seizure activity and convulsions and the animals appeared awake throughout the experiment. All animals exhibited bradycardia and hypotension following the adminstration of therapy. The cholinesterase activity was depressed after administration of HS-6 therapy. Three of the four monkey that received therapy consisting of HI-6 at a dose of 15 mg/kg survived, while one of two that received HI-6 at a dose of 30 mg/kg survived. The animals that received HI-6 at a dose of 15 mg/kg did not exhibit as severe a decrease in blood pressure as the animals in either the HS-6 series or the monkeys that received HI-6 at 30 mg/kg. In addition, these monkeys were awake and appeared alert throughout the experiment and were up within 4-6 hr post-exposure to soman. The animals that received 30 mg/kg exhibited severe hypotension and did poorly.

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Year:  1980        PMID: 7447543

Source DB:  PubMed          Journal:  Arch Int Pharmacodyn Ther        ISSN: 0003-9780


  10 in total

1.  Distribution of the bispyridinium oxime [14C] HI-6 in male and female rats.

Authors:  P M Lundy; B T Hand; B R Broxup; G Yipchuck; M G Hamilton
Journal:  Arch Toxicol       Date:  1990       Impact factor: 5.153

2.  In vitro oxime-induced reactivation of various molecular forms of soman-inhibited acetylcholinesterase in striated muscle from rat, monkey and human.

Authors:  J G Clement; N Erhardt
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

3.  HI-6 therapy of soman and tabun poisoning in primates and rodents.

Authors:  M G Hamilton; P M Lundy
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

4.  Treatment of organophosphate poisoning in pigs: antidote administration by a new binary autoinjector.

Authors:  A Göransson-Nyberg; G Cassel; T Jeneskog; L Karlsson; R Larsson; M Lundström; S A Persson
Journal:  Arch Toxicol       Date:  1995       Impact factor: 5.153

5.  Effect of pyridostigmine pretreatment, HI-6 and Toxogonin treatment on rat tracheal smooth muscle response to cholinergic stimulation after organophosphorus inhalation exposure.

Authors:  P Walday; P Aas; T Haider; F Fonnum
Journal:  Arch Toxicol       Date:  1993       Impact factor: 5.153

6.  Non-reactivating effects of HI-6 on hippocampal neurotransmission.

Authors:  B P Melchers; A L van der Laaken; R W Busker; P L Bruijnzeel; H P Van Helden
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

7.  Bioavailability of diazepam after intramuscular injection of its water-soluble prodrug alone or with atropine-pralidoxime in healthy volunteers.

Authors:  C Abbara; J M Rousseau; A Turcant; G Lallement; E Comets; I Bardot; P Clair; B Diquet
Journal:  Br J Pharmacol       Date:  2009-08       Impact factor: 8.739

8.  Pharmacokinetics and pharmacodynamics of the oxime HI6 in dogs.

Authors:  R Klimmek; P Eyer
Journal:  Arch Toxicol       Date:  1986-12       Impact factor: 5.153

9.  Treatment of tabun poisoned guinea-pigs with atropine, HLö 7 or HI 6: effect on respiratory and circulatory function.

Authors:  F Worek; T Kirchner; L Szinicz
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

10.  Comparison of the therapeutic effects and pharmacokinetics of HI-6, HLö-7, HGG-12, HGG-42 and obidoxime following non-reactivatable acetylcholinesterase inhibition in rats.

Authors:  H P van Helden; H J van der Wiel; J J Zijlstra; B P Melchers; R W Busker
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

  10 in total

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