Research Article

Naringin Protects against Tau Hyperphosphorylation in Aβ25–35-Injured PC12 Cells through Modulation of ER, PI3K/AKT, and GSK-3β Signaling Pathways

Figure 4

Effect of naringin on the viability of PC12 cells injured by Aβ25–35. Cell viability was measured by MTT assays after exposure to the following treatments. (a) PC12 cells were incubated with different concentrations of naringin (100 pM, 1 nM, 10 nM, 100 nM, 1 μM, 10 μM, 100 μM, and 1 mM) or E2 (1 nM) for 24 hours. (b) PC12 cells were incubated with naringin (100 pM, 1 nM, 10 nM, 100 nM, 1 μM, 10 μM, and 100 μM) or E2 (1 nM) for 2 hours, then treated with Aβ25–35 (20 μM) for another 24 hours. (c) PC12 cells were precultured with ICI182780 (1 μM) or LY294002 (50 μM) for 1 hour, then treated with naringin (1 μM) or E2 (1 nM) for 2 hours, and then treated with Aβ25–35 (20 μM) for another 24 hours; or precultured with LiCl (10 mM) for 2 hours, then treated with Aβ25–35 (20 μM) for another 24 hours. Data are expressed as the mean ± SD (). Compared with the untreated cells, *, **; compared with Aβ2s5–35-treated cells, ##; compared with the treatment group, ▲▲.
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