The effect of high pressure on glycine- and kainate-sensitive receptor channels expressed in Xenopus oocytes
- 22 November 1993
- journal article
- Published by The Royal Society in Proceedings Of The Royal Society B-Biological Sciences
- Vol. 254 (1340) , 131-137
- https://doi.org/10.1098/rspb.1993.0137
Abstract
The effect of high pressure on the response to glycine or kainate of voltage-clamped Xenopus oocytes micro-injected with messenger-RNA derived from either rat spinal cord or whole brain, respectively, has been investigated. Current responses were measured at 1 bar (= 10(5) Pa), 50 bar, 100 bar and 150 bar, with PO2 fixed at 1 bar and the balance helium. Glycine elicited a depolarizing current response which was antagonized by nanomolar concentrations of strychnine. The responses reversibly desensitized, with a decay constant of 0.01 s-1, when glycine concentrations greater than 250 microM were used. The decay constant was insensitive to both glycine concentration and pressure. Resensitization was complete within 4 min. Kainate elicited a depolarizing current which was non-desensitizing. The response was slightly sensitive to glutamate diethyl ester (50 microM), which increased the EC50 by 25%. The action of glycine was highly pressure sensitive. The dose-response curves established at 50 bar, 100 bar and 150 bar were shifted progressively to the right, with no effect on the maximal current. The EC50 increased from 216 microM to 296 microM at 50 bar, to 345 microM at 100 bar, and to 425 microM at 150 bar. The action of kainate was unaffected by pressure. No shift in the dose-response curves was established, nor was there any effect on the maximum current. The EC50 was 113 microM at 1 bar, and 111 microM at both 50 bar and 100 bar.(ABSTRACT TRUNCATED AT 250 WORDS)Keywords
This publication has 28 references indexed in Scilit:
- The Nicotinic Acetylcholine Receptor in Its Membrane EnvironmentaAnnals of the New York Academy of Sciences, 1991
- Responses to GABA, glycine and β-alanine induced in Xenopus oocytes by messenger RNA from chick and rat brainProceedings of the Royal Society of London. B. Biological Sciences, 1988
- Channel families in the brainNature, 1987
- The Use ofXenopusOocytes for the Study of Ion ChannelCritical Reviews in Biochemistry, 1987
- Species variation and the mechanism of pressure–anaesthetic interactionsNature, 1984
- Messenger RNA from human brain induces drug- and voltage-operated channels in Xenopus oocytesNature, 1984
- Mechanistic studies on the high pressure neurological syndromePhilosophical Transactions of the Royal Society of London. B, Biological Sciences, 1984
- The benzodiazepine antagonist, Ro 15-1788, prevents the effects of flurazepam on the high pressure neurological syndromeNeuropharmacology, 1982
- Diazepam Under Hyperbaric Conditions in RatsActa Anaesthesiologica Scandinavica, 1980
- Animals at Very High Pressures of Helium and NeonScience, 1967