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. Author manuscript; available in PMC: 2015 Dec 1.
Published in final edited form as: Anesth Analg. 2014 Dec;119(6):1277–1284. doi: 10.1213/ANE.0000000000000423

Figure 4.

Figure 4

F6 modulates α5β3γ2L but not α5β3(N265M)γ2L receptors at amnestic concentrations. A. Responses to a 500 ms-long application of 1 μM GABA to α5β3γ2L receptors (top) and to α5β3(N265M)γ2L receptors (bottom). B. Concentration-response relationships for α5β3γ2L and α5β3(N265M)γ2L receptors in the presence of F6 ranging from 4 to 16 μM, normalized to the peak amplitude under control conditions (absence of F6).