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. 2014 May 18;11:15. doi: 10.1186/1476-9255-11-15

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Copyright © 2014 Vester et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Post-incubation with GTE recovers osteoblast viability and reduces ROS production after induction of oxidative stress. Osteoblasts were treated for 1 h with 1 mM H₂O₂ followed by the stimulation with GTE for 4 h. Cell viability was measured via MTT assay (A). For flow cytometry, the osteoblasts were treated for 15 min. with H₂O₂ and stimulated with GTE for the next hour (B) (N = 3, n = 2). Bars represent mean ± s.e.m. ***p < 0.001 (ANOVA/Bonferroni).