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. 2015 Oct 25;172(22):5403–5413. doi: 10.1111/bph.13329

Table 1.

Pharmacological properties of wild‐type α1β3γ2S and mutant GABAA receptors

Subunit composition EC50 (μM) n H n
α1β3γ2S 61.9 ± 2.1 1.44 ± 0.03 7
α1I227Aβ3γ2S 24.3 ± 1.4 *** 1.18 ± 0.04 5
α1L231Aβ3γ2S 89.1 ± 6.6 ** 1.32 ± 0.07 5
α1M235Aβ3γ2S 19.4 ± 2.2 *** 1.25 ± 0.13 6
α1M235Wβ3γ2S 2.9 ± 0.4 *** 0.79 ± 0.06 6
α1L268Aβ3γ2S 15.7 ± 1.9 *** 1.19 ± 0.1 5
α1β3T262Aγ2S 116.7 ± 9.1 *** 1.41 ± 0.06 5
α1β3T262Sγ2S 6.4 ± 0.1 *** 1.33 ± 0.14 6
α1β3N265Sγ2S 57.2 ± 4.5 1.23 ± 0.09 6
α1β3T266Aγ2S 143.7 ± 14.0 *** 1.21 ± 0.08 6
α1β3R269Aγ2S 108.4 ± 5.9 *** 1.51 ± 0.05 5
α1β3M286Aγ2S 138.4 ± 9.2 *** 1.33 ± 0.08 5
α1β3M286Wγ2S 7.1 ± 0.3 *** 1.33 ± 0.14 7
α1β3F289Sγ2S 7.0 ± 1.2 *** 0.90 ± 0.08 7

EC50 concentrations (μM) and Hill coefficients (n H) are given for each receptor as mean ± SEM for n number of cells tested. Statistical significance of difference from wild‐type was calculated using a one‐way ANOVA followed by a Dunnett's mean comparison test. ** P < 0.01; *** P < 0.001.