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. 2021 Feb 10;21:59. doi: 10.1186/s12906-021-03240-2

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 6 — Effects of DSEH on cell apoptosis caused by H₂O₂-induced oxidative injury. Cell apoptosis was assessed by staining the cells with Annexin V and PI and performing on a flow cytometry instrument. In each graph, the lower left region (R3) represents viable cells (Annexin V (−) PI (−)); the lower right region (R4) represents early apoptotic cells (Annexin V (+) PI (−)); the upper right region (R5) represents late apoptotic cells (Annexin V (+) PI (+)); and the upper left region (R6) represents necrotic cells (Annexin V (−) PI (+)). H₂O₂: hydrogen peroxide