1. Academic Validation
  2. Nrf2 protects against seawater drowning-induced acute lung injury via inhibiting ferroptosis

Nrf2 protects against seawater drowning-induced acute lung injury via inhibiting ferroptosis

  • Respir Res. 2020 Sep 9;21(1):232. doi: 10.1186/s12931-020-01500-2.
Yu-Bao Qiu 1 Bin-Bin Wan 1 Gang Liu 1 Ya-Xian Wu 1 Dan Chen 1 Mu-Dan Lu 2 Jun-Liang Chen 1 Ren-Qiang Yu 2 Dao-Zhen Chen 3 Qing-Feng Pang 4
Affiliations

Affiliations

  • 1 Wuxi School of Medicine, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, Jiangsu Province, People's Republic of China.
  • 2 Central Laboratory, The Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University, 48 Huaishu Lane, Wuxi, 214122, Jiangsu Province, People's Republic of China.
  • 3 Central Laboratory, The Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University, 48 Huaishu Lane, Wuxi, 214122, Jiangsu Province, People's Republic of China. chendaozhen@163.com.
  • 4 Wuxi School of Medicine, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, Jiangsu Province, People's Republic of China. qfpang@jiangnan.edu.cn.
Abstract

Background: Ferroptosis is a new type of nonapoptotic cell death model that was closely related to Reactive Oxygen Species (ROS) accumulation. Seawater drowning-induced acute lung injury (ALI) which is caused by severe oxidative stress injury, has been a major cause of accidental death worldwide. The latest evidences indicate nuclear factor (erythroid-derived 2)-like 2 (Nrf2) suppress Ferroptosis and maintain cellular redox balance. Here, we test the hypothesis that activation of Nrf2 pathway attenuates seawater drowning-induced ALI via inhibiting Ferroptosis.

Methods: we performed studies using Nrf2-specific agonist (dimethyl fumarate), Nrf2 inhibitor (ML385), Nrf2-knockout mice and Ferroptosis inhibitor (Ferrostatin-1) to investigate the potential roles of Nrf2 on seawater drowning-induced ALI and the underlying mechanisms.

Results: Our data shows that Nrf2 activator dimethyl fumarate could increase cell viability, reduced the levels of intracellular ROS and lipid ROS, prevented glutathione depletion and lipid peroxide accumulation, increased FTH1 and GPX4 mRNA expression, and maintained mitochondrial membrane potential in MLE-12 cells. However, ML385 promoted cell death and lipid ROS production in MLE-12 cells. Furthermore, the lung injury became more aggravated in the Nrf2-knockout mice than that in WT mice after seawater drowning.

Conclusions: These results suggested that Nrf2 can inhibit Ferroptosis and therefore alleviate ALI induced by seawater drowning. The effectiveness of Ferroptosis inhibition by Nrf2 provides a novel therapeutic target for seawater drowning-induced ALI.

Keywords

Acute lung injury; Drowning; Ferroptosis; Nrf2; Seawater.

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