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. 2020 Aug 5;11:77. doi: 10.1186/s40104-020-00489-4

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© The Author(s) 2020

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. 4 — Mdivi-1 treatment induces oxidative stress in porcine oocytes. a The reactive oxygen species (ROS) level in the control and treatment groups of oocytes. Most control oocytes revealed weak ROS fluorescence signals, while the signals were much stronger in treated oocytes. Green, ROS. Bar = 20 μm. b ROS fluorescence intensity analysis. Fluorescence intensity was much higher in the treatment group oocytes than the control oocytes. c Superoxide dismutase (SOD)1 and SOD2 mRNA levels decreased significantly while the glutathione peroxidase (GPx) mRNA level increased significantly increased after inhibiting DRP1