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. 2019 Jun 25;19:149. doi: 10.1186/s12906-019-2559-8

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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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Fig. 3 — Effect of the studied extracts on the carbon tetrachloride (CCl₄)-induced oxidative stress in Vero Cells in comparison with the Ketosteril (Ks). (a) Flow cytometric analysis of ROS production in Vero cells using dichlorofluorescein (DCF) (b) Quantification of the DCF flow cytometric data (c) Thiobarbituric acid reactive substances (TBARS) level (d) Reduced glutathione (GSH) level (e) Superoxide dismutase (SOD) and glutathione peroxidase (GPX) activities. C; the untreated control cells, AVE, Ammi visnaga extract; PCE, Petroselinum crispum extract; HVE, Hordeum vulgare extract; CSE, Cymbopogon schoenanthus extract. Results are presented as mean ± SE (n = 3). Different letters for the same parameter are significantly different at p < 0.05