1. Academic Validation
  2. Dietary docosahexaenoic acid plays an opposed role in ferroptotic and non-ferroptotic acute kidney injury

Dietary docosahexaenoic acid plays an opposed role in ferroptotic and non-ferroptotic acute kidney injury

  • J Nutr Biochem. 2023 Jul 23;109418. doi: 10.1016/j.jnutbio.2023.109418.
Kai Shan 1 Jiaqi Li 2 Qin Yang 2 Kang Chen 3 Shanshan Zhou 4 Lingling Jia 5 Guoling Fu 2 Yumin Qi 2 Qizai Wang 3 Yong Q Chen 6
Affiliations

Affiliations

  • 1 College of Food Science and Technology, Nanjing Agricultural University, Nanjing, Jiangsu Province, 210095, China.
  • 2 Wuxi School of Medicine, Jiangnan University, Wuxi, Jiangsu Province, 214012, China; School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu Province, 214012, China.
  • 3 Food Sciences, Department of Life Technologies, University of Turku, Turku, FI-20014, Finland.
  • 4 The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, 210000, China.
  • 5 College of Food and Pharmaceutical Sciences, Ningbo University, Ningbo, Zhejiang Province, 315800, China.
  • 6 Wuxi School of Medicine, Jiangnan University, Wuxi, Jiangsu Province, 214012, China; School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu Province, 214012, China. Electronic address: [email protected].
Abstract

Ferroptosis due to polyunsaturated fatty acid (PUFA) peroxidation has been implicated in the pathogenesis of acute kidney injury (AKI), suggesting the risk of dietary intake of PUFA for people susceptible to AKI. Clinically, however, in addition to Ferroptosis, other mechanisms also contribute to different types of AKI such as inflammation associated Necroptosis and Pyroptosis. Therefore, the role of PUFA, especially ω3 PUFA which is a common food supplement, in various AKIs deserves further evaluation. In this study, rhabdomyolysis- and folic acid- induced AKI (Rha-AKI and FA-AKI) were established in mice fed with different fatty acids Histology of kidney, blood urea nitrogen and creatinine, lipid peroxidation, and inflammatory factors were examined. Results showed that these two types of AKIs had diametrically different pathogenesis indicated by that ferrostatin-1 (Fer-1), a lipid antioxidant, can attenuate FA-AKI rather than Rha-AKI. Further, dietary DHA (provided by fish oil) reduced tubular injury and renal lesion by inhibiting peroxidation and inflammation in mice with Rha-AKI while increasing cell death, tissue damage, peroxidation and inflammation in mice with FA-AKI. In human renal tubular epithelial cell line HK-2, MTT assay and DHE staining showed that both myoglobin and Ferroptosis inducers can cause cell death and oxidative stress. Ferroptosis inducer-induced cell death was promoted by DHA, while such result was not observed in myoglobin-induced cell death when adding DHA. This study illustrates that the mechanisms of AKI might be either Ferroptosis dependent or -independent and the deterioration effect of dietary DHA depends on whether Ferroptosis is involved.

Keywords

DHA; acute kidney injury; ferroptosis.

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