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. 2021 Apr 6;10(4):702. doi: 10.3390/plants10040702

Figure 2.

Figure 2

Protective effects of EEBC against H2O2-damaged HT22 neuronal cells. (a) Cells were incubated with various concentrations of EEBC for 24 h and cell viability evaluated using a Cell Counting Kit (CCK) assay; (b) Cells were co-treated with EEBC (0, 12.5, 25, or 50 μg/mL) and H2O2 (250 μM) for 6 h. CCK assay was performed to assess changes in cell viability. Caveolin was used as a positive control. Data are expressed as % of the control. Values represent mean ± SEM. ### p < 0.001 vs. untreated cells; * p < 0.05 and ** p < 0.01 vs. H2O2-treated cells; (c) Morphological changes in cells were observed under inverted microscopy (Eclipse TS100, Nikon, Japan). EEBC: ethanol extract of B. coccinea branches. CCK: Cell Counting Kit. PC: positive control.