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CORRECTION article

Front. Physiol., 29 March 2022
Sec. Vascular Physiology
Volume 13 - 2022 | https://doi.org/10.3389/fphys.2022.805972

Corrigendum: Propofol Alleviates DNA Damage Induced by Oxygen Glucose Deprivation and Reperfusion via FoxO1 Nuclear Translocation in H9c2 Cells

This article is a correction to:

  1. Propofol Alleviates DNA Damage Induced by Oxygen Glucose Deprivation and Reperfusion via FoxO1 Nuclear Translocation in H9c2 Cells

    1. Read original article
\nDandan Zhou&#x;Dandan Zhou1†Jinqiang Zhuang&#x;Jinqiang Zhuang1†Yihui WangYihui Wang1Dandan ZhaoDandan Zhao1Lidong ZhaoLidong Zhao1Shun Zhu,Shun Zhu1,2Jinjun PuJinjun Pu3Ming YinMing Yin2Hongyu ZhangHongyu Zhang4Zejian Wang Zejian Wang2*Jiang Hong Jiang Hong1*
  • 1Department of Internal and Emergency Medicine, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China
  • 2School of Pharmacy, Shanghai Jiao Tong University, Shanghai, China
  • 3Department of Emergency Medicine, Putuo Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China
  • 4Department of Biomedicine, KG Jebsen Centre for Research on Neuropsychiatric Disorders, University of Bergen, Bergen, Norway

A Corrigendum on
Propofol Alleviates DNA Damage Induced by Oxygen Glucose Deprivation and Reperfusion via FoxO1 Nuclear Translocation in H9c2 Cells

by Zhou, D., Zhuang, J., Wang, Y., Zhao, D., Zhao, L., Zhu, S., Pu, J., Yin, M., Zhang, H., Wang, Z., and Hong, J. (2019). Front. Physiol. 10:223. doi: 10.3389/fphys.2019.00223

In Figure 2 of the article, we provided the wrong image of the DMSO group. The correct Figure 2 is displayed below.

FIGURE 2
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Figure 2. Propofol inhibited cell apoptosis induced by OGD/R in H9c2 cells. Quantification of the apoptotic cell population by flow cytometry. Propofol decreased the percentage of apoptotic cells compared with the model. The data are presented as the mean ± SD of three independent experiments. *p < 0.05, **p < 0.01, ***p < 0.001 versus control, #p < 0.05, ##p < 0.01, ###p < 0.001 versus OGD/R treated group without drugs.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: propofol, oxygen glucose deprivation and reperfusion, ROS, DNA damage, FoxO1

Citation: Zhou D, Zhuang J, Wang Y, Zhao D, Zhao L, Zhu S, Pu J, Yin M, Zhang H, Wang Z and Hong J (2022) Corrigendum: Propofol Alleviates DNA Damage Induced by Oxygen Glucose Deprivation and Reperfusion via FoxO1 Nuclear Translocation in H9c2 Cells. Front. Physiol. 13:805972. doi: 10.3389/fphys.2022.805972

Received: 31 October 2021; Accepted: 28 February 2022;
Published: 29 March 2022.

Edited and reviewed by: Tommaso Angelone, University of Calabria, Italy

Copyright © 2022 Zhou, Zhuang, Wang, Zhao, Zhao, Zhu, Pu, Yin, Zhang, Wang and Hong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Zejian Wang, d2FuZ3plamlhbiYjeDAwMDQwO3NqdHUuZWR1LmNu; Jiang Hong, amhvbmcucGt1JiN4MDAwNDA7MTYzLmNvbQ==

†These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.