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. Author manuscript; available in PMC: 2009 Apr 13.
Published in final edited form as: Anesth Analg. 2008 Sep;107(3):868–874. doi: 10.1213/ane.0b013e31817ee500

Fig 4.

Fig 4

α1 Glycine receptors expressed in Xenopus oocytes were significantly potentiated by isoflurane, ethanol, and six surfactants and inhibited by one (SDS) (all effects are significantly different from zero, P<0.05). Summary bar graphs show the mean glycine-induced responses, at EC5 agonist concentrations, from multiple oocytes expressing α1 glycine receptors in the presence of study compounds. Means ± SE (N = 4–7) are displayed. SDS = sodium dodecyl sulfate, SOS = sodium n-octyl sulfate, OTABR = (1-octyl)trimethylammonium bromide, DTACL = (1dodecyl) trimethylammonium chloride, DAPS = 3-(dodecyldimethylammonio)propanesulfonate. C12 = 12 carbon tail, C8 = 8 carbon tail for the surfactants. Anionic, cationic, zwitterionic, and uncharged refer to head group charges for the surfactants.