{"title":"Comparative effects of ethanol and other depressant drugs on membrane order in rat synaptosomes using ESR spectroscopy.","authors":"B J Logan, R Laverty","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The effects of ethanol, t-butanol and pentobarbitone on the membrane order of rat synaptosomal membranes have been compared using 3 spin-label probes, 5-doxyl-stearic acid which reports from a lipid site near the membrane surface, 16-doxyl-stearic acid which reports from a deeper lipid site, and maleimide-TEMPO which covalently binds to membrane protein. The sensitivity of the membrane proteins to a fluidizing effect of ethanol was increased by lowering the concentration of protein-binding probe. Significant decreases in membrane order were observed at anaesthetic concentrations of ethanol and t-butanol with all three probes; pentobarbitone produced a similar effect but only at very high concentrations. Pentobarbitone caused a marked change in high-field peak shape of the 16-doxyl-stearic acid spectra at anaesthetic concentrations; this effect was seen slightly with t-butanol and trichlorethanol but not with ethanol. These studies indicate that the membrane sites of action of ethanol and pentobarbitone as shown by ESR probes are different.</p>","PeriodicalId":7671,"journal":{"name":"Alcohol and drug research","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1987-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alcohol and drug research","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The effects of ethanol, t-butanol and pentobarbitone on the membrane order of rat synaptosomal membranes have been compared using 3 spin-label probes, 5-doxyl-stearic acid which reports from a lipid site near the membrane surface, 16-doxyl-stearic acid which reports from a deeper lipid site, and maleimide-TEMPO which covalently binds to membrane protein. The sensitivity of the membrane proteins to a fluidizing effect of ethanol was increased by lowering the concentration of protein-binding probe. Significant decreases in membrane order were observed at anaesthetic concentrations of ethanol and t-butanol with all three probes; pentobarbitone produced a similar effect but only at very high concentrations. Pentobarbitone caused a marked change in high-field peak shape of the 16-doxyl-stearic acid spectra at anaesthetic concentrations; this effect was seen slightly with t-butanol and trichlorethanol but not with ethanol. These studies indicate that the membrane sites of action of ethanol and pentobarbitone as shown by ESR probes are different.