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. Author manuscript; available in PMC: 2017 May 1.
Published in final edited form as: Biol Psychiatry. 2015 Jun 5;79(9):746–754. doi: 10.1016/j.biopsych.2015.05.018

Table 2.

Sensitivity of NMDAR-mediated synaptic currents to GluN2B antagonist ifenprodil over early postnatal development.

P15 P30 P45
N/A Ratio n P N/A Ratio n P N/A Ratio n P
Pyramidal Neurons
Mecp2 WT Control 1.18±0.08 15 ** 0.96±0.09 9 n.s. 0.92±0.05 13 n.s.
Ifenprodil 0.83±0.09 12 0.81±0.08 13 0.82±0.05 14
Mecp2 KO Control 1.02±0.05 15 ** 0.96±0.07 11 ** 0.91±0.04 18 *
Ifenprodil 0.78±0.06 10 0.64±0.08 9 0.78±0.05 10
Parvalbumin Interneurons
Mecp2 WT Control 1.24±0.09 12 ** 0.75±0.06 11 ** 0.63±0.08 11 n.s.
Ifenprodil 0.56±0.09 12 0.47±0.06 11 0.46±0.09 10
Mecp2 KO Control 1.06±0.08 13 ** 0.60±0.05 10 n.s. 0.66±0.07 12 n.s.
Ifenprodil 0.66±0.09 10 0.48±0.05 11 0.55±0.07 13

N/A Ratio = Ratio of NMDAR-/AMPAR-mediated synaptic currents; n=number of cells;

**

P <0.01,

*

P <0.02,

ANOVA with Bonferroni correction for multiple comparisons