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. Author manuscript; available in PMC: 2020 Jun 29.
Published in final edited form as: Neuropharmacology. 2019 Jan 30;149:45–54. doi: 10.1016/j.neuropharm.2019.01.021

Fig. 5.

Fig. 5

Effects of 0.5 mM EtOH on function of different nAChR subtypes heterologously expressed in SH-EP1 cells (α4β2- and α7-nAChRs) or naturally expressed in SH-SY5Y cells (α3β4*-nAChRs) A: Representative traces of nAChR-mediated current responses to agonists at their EC50 concentrations before and after exposure to 0.5 mM EtOH. When ACh was applied as an agonist (left traces) of α3β4-nAChRs, 1 μM atropine was added in in external solution. B: Summary of the pooled data to show effects of 0.5 mM EtOH on current peak amplitudes of three subtypes of nAChR-mediated currents.