Literature DB >> 42547

Ganglion blocking properties of some bispyridinium soman antagonists.

P M Lundy, K P Tremblay.   

Abstract

Various doses of several bispyridinium compounds (HS-6, HI-6, HGG-12, HGG-42, and SAD-128) known to protect animals against the irreversible cholinesterase inhibitor soman were examined to determine their effects on the cardiovascular and respiratory system of cats. Although the potency varied considerably all of the compounds tested lowered the blood pressure, which appeared to be the result of ganglion blocking properties as determined by their reduction of the pressor response to dimethylphenylpiperazinium and the blockage of the contraction of the preganglionically stimulated cat nictitating membrane. Some of the compounds caused cessation of respiration at much lower doses than others but did so at doses greater than those causing ganglion blockage.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 42547     DOI: 10.1016/0014-2999(79)90051-7

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  18 in total

1.  The acetylcholinesterase reactivator HI-6 (1-[[[4-(aminocarbonyl)pyridinio]methoxyl]methyl]- 2-[(hydroxyimino)methyl]-pyridinium dichloride): a comparative study of HI-6 samples from various sources.

Authors:  J G Clement; P A Lockwood; H G Thompson
Journal:  Arch Toxicol       Date:  1988       Impact factor: 5.153

2.  Studies on the role of central catecholaminergic mechanisms in the antidotal effect of the oxime HI 6 in soman poisoned mice.

Authors:  C Reithmann; H Arbogast; M Hallek; G Auburger; L Szinicz
Journal:  Arch Toxicol       Date:  1988-08       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.  Receptor-mediated presynaptic facilitation of quantal release of acetylcholine induced by pralidoxime in Aplysia.

Authors:  P Fossier; G Baux; B Poulain; L Tauc
Journal:  Cell Mol Neurobiol       Date:  1990-09       Impact factor: 5.046

5.  Ion channel blockade by oximes and recovery of diaphragm muscle from soman poisoning in vitro.

Authors:  J E Tattersall
Journal:  Br J Pharmacol       Date:  1993-04       Impact factor: 8.739

6.  The oxime HGG-12 as a muscarinic acetylcholine receptor antagonist without intrinsic activity in cardiac membranes.

Authors:  C Reithmann; H J Berger; G Hilf; K Werdan
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

7.  Reactivators of organophosphate-inhibited cholinesterase. Phenylhydroxymethyl and cyclohexylhydroxymethyl substituted bis-pyridinium monooximes.

Authors:  V Deljac; M Maksimović; L Radović; D Rakin; V Markov; I Bregovec; Z Binenfeld
Journal:  Arch Toxicol       Date:  1982-03       Impact factor: 5.153

8.  Interactions of bisquaternary pyridine salts (H-oximes) with cholinergic receptors.

Authors:  D Kuhnen-Clausen; I Hagedorn; G Gross; H Bayer; F Hucho
Journal:  Arch Toxicol       Date:  1983-11       Impact factor: 5.153

9.  Bispyridinium (oxime) compounds antagonize the "ganglion blocking" effect of pyridostigmine in isolated superior cervical ganglia of the rat.

Authors:  C Schlagmann; H Ulbrich; J Remien
Journal:  Arch Toxicol       Date:  1990       Impact factor: 5.153

10.  Noncholinesterase actions of an irreversible acetylcholinesterase inhibitor on synaptic transmission and membrane properties in autonomic ganglia.

Authors:  P Yarowsky; J C Fowler; G Taylor; D Weinreich
Journal:  Cell Mol Neurobiol       Date:  1984-12       Impact factor: 5.046

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.