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. 2016 Dec;90(6):689–702. doi: 10.1124/mol.116.105130

TABLE 6.

Effects of (+)-CIQ on the AMPAR and NMDAR components of mEPSCs in P7–14 mice

AMPAR Amplitudea
NMDAR Amplitudeb
n
Control (pA) Treatment (pA) Treatment/Control Control (pA) Treatment (pA) Treatment/Control
Interneuron
WT Vehicle 18 ± 3.4 19 ± 3.3 1.07 ± 0.21 1.4 ± 0.25 1.6 ± 0.26 1.15 ± 0.22 8
WT (+)-CIQ 20 ± 1.8 20 ± 1.7 0.99 ± 0.03 1.2 ± 0.12 1.7 ± 0.11* 1.47 ± 0.10 17
Grin2d−/− (+)-CIQ 24 ± 4.3 23 ± 5.3 0.95 ± 0.21 1.8 ± 0.17 1.6 ± 0.20 0.90 ± 0.20 4
Pyramidal
WT Vehicle 23 ± 2.6 19 ± 1.8 0.85 ± 0.16 2.5 ± 0.89 3.0 ± 1.0 1.33 ± 0.27 7
WT (+)-CIQ 20 ± 1.6 19 ± 2.4 0.94 ± 0.15 2.9 ± 0.32 3.0 ± 0.29 1.09 ± 0.19 10
a

AMPAR amplitudes were measured by the amplitude of fast component of the fitted composite mEPSC (mean ± S.E.M.).

b

NMDAR amplitudes were measured as the averaged response between 40 and 50 ms after the peak AMPAR response (mean ± S.E.M.).

*

P < 0.05, Dunnett’s test after a repeat-measure ANOVA (control versus treatment).