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Figure 3


Figure 3. O3 amino acids selectively inhibited the NF-{kappa}B system. (A) HeLa cells were incubated with O3-phosphate-buffered saline (1 hr), followed by TNF stimulation (1 ng/mL, 15 min). The ozonation state is indicated in %. We performed an electrophoretic mobility shift assay to determine NF-{kappa}B activity as well as Sp-1 binding. (B) Cells were pre-incubated (1 hr) with non-ozonized or ozonized amino acids (medium concentration) dissolved in phosphate-buffered saline (100% ozonation state), followed by stimulation with TNF (1 ng/mL, 15 min). The activation of NF-{kappa}B was determined by an electrophoretic mobility shift assay. (C) Densitometric analysis of the NF-{kappa}B activity normalized to Sp-1 is shown (n = 3, mean ± SD). NF-{kappa}B activity of cells pre-incubated with non-ozonized amino acids in phosphate-buffered saline and stimulated with TNF was defined as 100% (dashed line). (D) HeLa cells were pre-incubated with non-ozonized or ozonized glucose (medium concentration), followed by TNF stimulation. The NF-{kappa}B activity compared with Sp-1 binding was determined by an electrophoretic mobility shift assay.





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IADR Journals Advances in Dental Research ®
Journal of Dental Research ® Critical Reviews (1990-2004)