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. 2011 Nov;339(2):386–393. doi: 10.1124/jpet.111.184408

Fig. 5.

Fig. 5.

The increase in ethanol sensitivity produced by activated Gαs depends on βγ subunits. A, whole-cell recordings obtained in HEK293 cells that coexpressed Gαs Q-L and the Gβγ sequester ct-GRK2. Current traces during the application of 1 and 100 mM ethanol are shown. B, concentration response curves for ethanol (1–200 mM) show that the shift in the ethanol sensitivity promoted by Gαs Q-L (■) is blocked by expression of the Gβγ sequester (●). Differences were significant (***, P < 0.001, ANOVA). C, traces are Cl currents induced in two α1 GlyRs with intracellular mutations in cells overexpressing Gαs Q-L during the application of different ethanol concentrations. D, graph shows that the expression of the constitutively active Gαs did not modify the ethanol sensitivity of either 316–320A (■) or 385–386A (●) mutated GlyRs with respect to cells expressing Gαs Q-L (○ and □). Differences were not significant.