Pretreatment with cinnamic aldehyde or ethanolic cinnamon extract protects HCT116 colon cancer cells against oxidative stress-induced geno- and cytotoxicity. Cells were exposed to CA (5 μM, panel a) or CE (dose CA: 5 μM, panel b) for 24 h. After media change, oxidative genotoxic stress was induced by addition of H2O2 (100 μM, 30 min), and DNA damage was detected using the Comet assay as decribed in Materials and Methods. Bottom panels depict representative comets as visualized by fluorescence microscopy. (mean ± SEM, n=3; means with common letter differ, p<0.05).
(c) Cells pretreated as indicated above underwent short-term exposure to H2O2 (500 μM, 6 h) followed immediately by assessment of cellular ATP levels using the Celltiter-Glo assay as described in Material and Methods. (mean ± SEM, n=3; means with common letter differ, p<0.05). (d) Cells were pre-treated with CA (2.5 μM, upper panel), CE (dose CA: 2.5 μM, lower panel), or solvent only (DMSO) for 24 h followed by co-treatment with the indicated concentrations of sodium arsenite (up to 80 μM) for 48 h. Cell viability was then determined using the MTT assay as detailed in Material and Methods. (mean ± SEM, n=3; p<0.05)