Abstract
The structural organization of membrane proteins and their interaction with lipids renders them sensitive to perturbations of organic solvents. Some membrane proteins are inhibited up to 50 per cent at the anaesthetic concentration of many inhalation anaesthetics, aliphatic and aromatic hydrocarbons, alcohols, ketones, esters and alkanes (Franks and Lieb 1982). Hydrophilic pockets of proteins may bind anaesthetics with high selectivity and cause conformational changes. Changes of the allosteric properties of membrane proteins may provide a possible mechanism of anaesthesia. The aim of the present study was to evaluate whether peripheral erythrocyte and platelet membranes as well as cerebral synaptosome membranes can be used in determinations of the anaesthetic potency of organic solvents.
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References
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© 1991 Springer-Verlag Berlin Heidelberg
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Tähti, H., Valaja, A. (1991). The Mechanism of the Anaesthetic Action of Organic Solvents Studied with Different Membrane Models in Vitro. In: Chambers, P.L., Chambers, C.M., Wiezorek, W.D., Golbs, S. (eds) Recent Developments in Toxicology: Trends, Methods and Problems. Archives of Toxicology, vol 14. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-74936-0_57
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DOI: https://doi.org/10.1007/978-3-642-74936-0_57
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-51422-0
Online ISBN: 978-3-642-74936-0
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