4.6 Article

Epigallocatechin Gallate Attenuates Gentamicin-Induced Nephrotoxicity by Suppressing Apoptosis and Ferroptosis

Journal

MOLECULES
Volume 27, Issue 23, Pages -

Publisher

MDPI
DOI: 10.3390/molecules27238564

Keywords

nephrotoxicity; gentamicin; apoptosis; ferroptosis; epigallocatechin-3-gallate; Nrf2; GPX4

Funding

  1. National Natural Science Foundation of China
  2. Introduction and Stabilization of Talent Projects of Anhui Agricultural University
  3. Natural Science Projects for Colleges and Universities in the Anhui Province
  4. [81800606]
  5. [yj2020-64]
  6. [KJ2021A0140]

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This study demonstrated that epigallocatechin gallate (EG) from green tea attenuated nephrotoxicity induced by gentamicin (GEN), reducing the increase of ROS and MDA and the decrease of GSH levels, and activating the protein levels of Nrf2 and HO-1. Furthermore, EG alleviated apoptosis and ferroptosis caused by GEN. However, the protective effects of EG were weakened when Nrf2 was knocked down.
Gentamicin (GEN) is a kind of aminoglycoside antibiotic with the adverse effect of nephrotoxicity. Currently, no effective measures against the nephrotoxicity have been approved. In the present study, epigallocatechin gallate (EG), a useful ingredient in green tea, was used to attenuate its nephrotoxicity. EG was shown to largely attenuate the renal damage and the increase of malondialdehyde (MDA) and the decrease of glutathione (GSH) in GEN-injected rats. In NRK-52E cells, GEN increased the cellular ROS in the early treatment phase and ROS remained continuously high from 1.5 H to 24 H. Moreover, EG alleviated the increase of ROS and MDA and the decrease of GSH caused by GEN. Furthermore, EG activated the protein levels of nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1). After the treatment of GEN, the protein level of cleaved-caspase-3, the flow cytometry analysis and the JC-1 staining, the protein levels of glutathione peroxidase 4 (GPX4) and SLC7A11, were greatly changed, indicating the occurrence of both apoptosis and ferroptosis, whereas EG can reduce these changes. However, when Nrf2 was knocked down by siRNA, the above protective effects of EG were weakened. In summary, EG attenuated GEN-induced nephrotoxicity by suppressing apoptosis and ferroptosis.

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