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. 2018 Jun 25;9:2459. doi: 10.1038/s41467-018-04883-5

Fig. 7.

Fig. 7

TNFα causes serotonergic impairments in Eif4e ki/ki mice. a Representative sEPSC traces from mPFC pyramidal neurons in brain slices of wild-type mice treated with vehicle (saline), DN TNF (200 ng ml−1) or mouse recombinant TNFα (10 ng ml1). Synaptic currents were recorded before (baseline) and after 5-HT (20 μM) administration. b Representative sEPSC traces from Eif4e ki/ki mice treated with either vehicle or DN TNF (200 ng ml−1), measured before and after 5-HT (20 μM) administration. c Frequency of sEPSCs in mPFC slices of male and female wild-type mice. Slices were directly treated with saline (M: n = 10 cells from 6 mice; F: n = 9 cells from 6 mice), DN TNF (200 ng ml−1; M: n = 8 cells from 5 mice; F: n = 7 cells from 4 mice) or mouse recombinant TNFα (10 ng ml−1; M: n = 9 cells from 6 mice; F: n = 6 cells from 5 mice), pre- and post-5-HT (20 μM) application. d Average sEPSC frequency in Eif4e ki/ki mice before and after 5-HT (20 μM) application; slices were treated with either saline (M: n = 11 cells from 6 mice; F: n = 9 cells from 7 mice) or DN TNF (200 ng ml−1; M: n = 8 cells from 6 mice; F: n = 9 cells from 7 mice). e, Firing rate of DR neurons in wild-type and Eif4e ki/ki mice chronically treated with DN TNF or saline (ICV, 12 days; n = 33 recordings from 6 Eif4e+/+ Saline mice; n = 31 recordings from 5 Eif4e+/+ DN TNF mice; n = 16 recordings from Eif4e ki/ki Saline mice; n = 33 recordings from 6 Eif4e ki/ki DN TNF mice). * p < 0.05, ** p < 0.01, *** p < 0.001 vs. wild-type saline; & p < 0.05, && p < 0.01, &&& p < 0.001 vs. saline-treated Eif4e+/+or ki/ki (see Supplementary Table 2 for detailed results of statistical tests)