The ganglionic blocking properties of the cholinesterase reactivator, HS-6
Author:
- Paul M. LundyPLPaul M. Lundy
- 1 October 1978
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Physiology and Pharmacology
- Vol. 56 (5) , 857-862
Abstract
Following intravenous administration of the cholinesterase reactivator HS-6 (30 mg/kg), blood pressure fell (up to 50 mmHg) and maximal blood levels of HS-6 reached 242 μg/ml. HS-6 attenuated the pressor response resulting from carotid occlusion and the depressor effect of vagal stimulation. Doses of HS-6 below those used to protect against soman in different animal species (10–30 μmol/kg) progressively blocked the ganglion-stimulating effects of nicotine and dimethylphenylpiperazinium but not the pressor effect following adrenaline, a pattern similar to that produced by hexamethonium but only [ ] as potent. HS-6, like hexamethonium and mecamylamine, progressively blocked the contraction of the nictitating membrane of the cat resulting from preganglionic stimulation.The results indicate that HS-6 possesses ganglion-blocking properties at doses likely to be used in the protection against soman poisoning. The ganglion-blocking properties of the drug may be a factor in the beneficial effects of HS-6.Keywords
This publication has 3 references indexed in Scilit:
- The dependence of the blood level of the oxime HS-6 on the severity of organophosphate poisoningEuropean Journal of Pharmacology, 1976
- Therapeutic effects of HS-3, HS-6, benactyzine, and atropine in soman poisoning of dogsArchives of Toxicology, 1976
- PYRIDINE-2-ALDOXIME METHIODIDE IN THE TREATMENT OF SARIN AND TABUN POISONING, WITH NOTES ON ITS PHARMACOLOGYThe Journal of Pharmacology and Experimental Therapeutics, 1957