Affiliation:
1. Pathology and Toxicology Section, Research Laboratories, Food and Drug Directorate, Department of National Health and Welfare, Ottawa, Canada
Abstract
Abstract
The simultaneous administration of ethanol at doses of either 2, 3, or 4 g/kg intraperitoneally produced a dose-related decrease in the intraperitoneal LD50 for thiopentone, pentobarbitone, amylobarbitone, phenobarbitone and barbitone in rats. The most marked ethanol-barbiturate interaction was with the long-acting, poorly metabolized, less potent barbiturates phenobarbitone and barbitone. Similarly, a non-hypnotic dose of ethanol (3 g/kg, i.p.) produced a much greater prolongation of the sleeping time with non-hypnotic doses of phenobarbitone and barbitone, than with threshold doses of the shorter acting barbiturates. Various postulates are advanced to explain the underlying mechanism of the barbiturate-ethanol interaction.
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
Cited by
24 articles.
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