Literature DB >> 655442

The pressure reversal of a variety of anesthetic agents in mice.

K W Miller, M W Wilson.   

Abstract

The aim of this work was to study in mammals the ability of high pressures to reverse the anesthesia produced by a wide range of general anesthetics. Dose-response curves were obtained using mice at pressures ranging from 1 to 125 atm for five agents, namely alpha-chloralose, ethylcarbamate, phenobarbital and, for comparison, nitrogen and argon. The increase of ED50 was found to be a linear function of pressure in each case, but the proportionate increases in ED50 with pressure were greater for the three non-inhalation agents than for the two gases. Thus, the ratio of ED50 at 100 atm to that at 1 atm was 1.74 for alpha-chloralose, 1.68 for ethylcarbamate, and 1.54 for phenobarbital. On the other hand, the corresponding ratios for argon and nitrogen were only 1.36 and 1.34. The potencies of three short-acting agents (trichloroethanol, ketamine, and alphadione) were shown to increase with decreasing pressure, although ED50 values could not be obtained. It is concluded that pressure reverses the actions of a wide variety of anesthetics in mice. The results of this study are not inconsistent with either the fluidized lipid membrane or the critical volume hypotheses of anesthetic action.

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Year:  1978        PMID: 655442     DOI: 10.1097/00000542-197802000-00005

Source DB:  PubMed          Journal:  Anesthesiology        ISSN: 0003-3022            Impact factor:   7.892


  10 in total

1.  Anesthetic inhibition of firefly luciferase, a protein model for general anesthesia, does not exhibit pressure reversal.

Authors:  G W Moss; W R Lieb; N P Franks
Journal:  Biophys J       Date:  1991-12       Impact factor: 4.033

2.  Pressure reversal of alphaxalone/alphadolone and methohexitone in tadpoles: evidence for different molecular sites for general anaesthesia.

Authors:  M J Halsey; B Wardley-Smith; S Wood
Journal:  Br J Pharmacol       Date:  1986-10       Impact factor: 8.739

3.  Reduced lethality from ethanol or ethanol plus pentobarbital in mice exposed to 1 or 12 atmospheres absolute helium-oxygen.

Authors:  R D Malcolm; D A Finn; P J Syapin; R L Alkana
Journal:  Psychopharmacology (Berl)       Date:  1985       Impact factor: 4.530

4.  The physiological effects of hydrostatic pressure are not equivalent to those of helium pressure on Rana pipiens.

Authors:  B A Dodson; Z W Furmaniuk; K W Miller
Journal:  J Physiol       Date:  1985-05       Impact factor: 5.182

Review 5.  Molecular targets and mechanisms for ethanol action in glycine receptors.

Authors:  Daya I Perkins; James R Trudell; Daniel K Crawford; Ronald L Alkana; Daryl L Davies
Journal:  Pharmacol Ther       Date:  2010-04-23       Impact factor: 12.310

6.  Hyperbaric ethanol antagonism in mice: studies on oxygen, nitrogen, strain and sex.

Authors:  R L Alkana; R D Malcolm
Journal:  Psychopharmacology (Berl)       Date:  1982       Impact factor: 4.530

7.  Investigations into pharmacological antagonism of general anaesthesia.

Authors:  H J Little; A Clark; W P Watson
Journal:  Br J Pharmacol       Date:  2000-04       Impact factor: 8.739

Review 8.  Bench-to-bedside review: Molecular pharmacology and clinical use of inert gases in anesthesia and neuroprotection.

Authors:  Robert Dickinson; Nicholas P Franks
Journal:  Crit Care       Date:  2010-08-12       Impact factor: 9.097

9.  Effects of ketamine and of high pressure on the responses to gamma-aminobutyric acid of the rat superior cervical ganglion in vitro.

Authors:  H J Little
Journal:  Br J Pharmacol       Date:  1982-10       Impact factor: 8.739

10.  The effects of anaesthetics and high pressure on the responses of the rat superior cervical ganglion in vitro.

Authors:  H J Little; D L Thomas
Journal:  J Physiol       Date:  1986-05       Impact factor: 5.182

  10 in total

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