Fig. 6.
Effect of (R,S)-norketamine on the levels of phospho-active forms of mammalian target of rapamycin (mTOR), protein kinase B (Akt), extracellular signal–regulated kinases (ERK1/2), p70S6 kinase (p70S6K), and eukaryotic initiation factor 4E binding protein (4E-BP1) in PC-12 cells. (A) Cells were treated with different concentrations of (R,S)-norketamine (0–1 μM) for 1 h and processed for Western blot analysis. (B) Scatter plots illustrating the relative ratio of phosphorylated versus total forms of mTOR, Akt, ERK1/2, p70S6K, and 4E-BP1 in response to cell treatment with 25 nM of (R,S)-norketamine are shown (n = 3 independent experiments). *, **P < 0.05, 0.01 (ANOVA) compared with control cells.

Effect of (R,S)-norketamine on the levels of phospho-active forms of mammalian target of rapamycin (mTOR), protein kinase B (Akt), extracellular signal–regulated kinases (ERK1/2), p70S6 kinase (p70S6K), and eukaryotic initiation factor 4E binding protein (4E-BP1) in PC-12 cells. (A) Cells were treated with different concentrations of (R,S)-norketamine (0–1 μM) for 1 h and processed for Western blot analysis. (B) Scatter plots illustrating the relative ratio of phosphorylated versus total forms of mTOR, Akt, ERK1/2, p70S6K, and 4E-BP1 in response to cell treatment with 25 nM of (R,S)-norketamine are shown (n = 3 independent experiments). *, **P < 0.05, 0.01 (ANOVA) compared with control cells.

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