SIGMOIDAL COMPRESSION RATE-DEPENDENCE OF INERT-GAS NARCOTIC POTENCY IN RATS - IMPLICATION FOR LIPID VS. PROTEIN THEORIES OF INERT-GAS ACTION IN THE CENTRAL-NERVOUS-SYSTEM

Citation
Jh. Abraini et al., SIGMOIDAL COMPRESSION RATE-DEPENDENCE OF INERT-GAS NARCOTIC POTENCY IN RATS - IMPLICATION FOR LIPID VS. PROTEIN THEORIES OF INERT-GAS ACTION IN THE CENTRAL-NERVOUS-SYSTEM, Brain research, 808(2), 1998, pp. 300-304
Citations number
30
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
00068993
Volume
808
Issue
2
Year of publication
1998
Pages
300 - 304
Database
ISI
SICI code
0006-8993(1998)808:2<300:SCROIN>2.0.ZU;2-N
Abstract
Inert gases at raised pressure exert anaesthetic effects. It is assume d that anaesthesia by the inert gases is fundamentally similar to anae sthesia produced by general anaesthetics. However, do general anaesthe tics bind directly to proteins or influence activity by indirectly per turbing membrane lipids still remains a major question. Although the p ressure required to achieve anaesthesia with inert gases has been sugg ested to exert potentially some pressure antagonism per se, this has n ot been studied yet to our knowledge. We investigated this possibility using nitrogen, argon, and nitrous oxide. Whatever the narcotic agent used, our results showed that the pressure of narcotic required to in duce anaesthetic effects increased, as compression rate increased, in a sigmoid fashion rather than in a linear fashion. Evidence for sigmoi dal responses vs. linear responses depended of the narcotic potency of the anaesthetic agent used (nitrogen: r(2) = 0.973 vs, r(2) = 0.941; argon: r(2) = 0.971 vs. r(2) = 0.866; nitrous oxide: r(2) = 0.995 vs. r(2) = 0.879). Since a linear antagonism is predicted by Lipid theorie s, we think it likely that these findings indicate that inert gases bi nd to a modulatory site of a protein receptor and act as allosteric mo dulators. Since other workers provided evidence for binding processes using volatile anaesthetics, the present findings could indicate that all classes of general anaesthetics, including inert gases, could act by binding directly to proteins rather than by dissolving in some lipi ds of the cellular membrane. (C) 1998 Elsevier Science B.V. All rights reserved.