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  Indian J Med Microbiol
 

Figure 4: Millingtonia hortensis promoted cell survival and inhibited apoptosis in H2O2 treated SK-N-SH cells. The SK-N-SH cells were prior treated with H2O2 for 4 h and then discard the media and replaced with Millingtonia hortensis or His treatment for 24 h. The cell viability was analyzed by using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and the number of apoptotic cells was investigated by flow cytometry. The values present the mean ± standard error of the mean from 3 independent experiments. **P < 0.01, ***P < 0.001, in comparison with the control treatment;#P < 0.05,##P < 0.01,###P < 0.001, in comparison with the H2O2 treatment alone

Figure 4: <i>Millingtonia hortensis</i> promoted cell survival and inhibited apoptosis in H<sub>2</sub>O<sub>2</sub> treated SK-N-SH cells. The SK-N-SH cells were prior treated with H<sub>2</sub>O<sub>2</sub> for 4 h and then discard the media and replaced with <i>Millingtonia hortensis</i> or His treatment for 24 h. The cell viability was analyzed by using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and the number of apoptotic cells was investigated by flow cytometry. The values present the mean ± standard error of the mean from 3 independent experiments. **<i>P</i> < 0.01, ***<i>P</i> < 0.001, in comparison with the control treatment;<sup>#</sup><i>P</i> < 0.05,<sup>##</sup><i>P</i> < 0.01,<sup>###</sup><i>P</i> < 0.001, in comparison with the H<sub>2</sub>O<sub>2</sub> treatment alone