Epigallocatechin Gallate Attenuates Gentamicin-Induced Nephrotoxicity by Suppressing Apoptosis and Ferroptosis.
Lin YueYa-Ru YangWen-Xian MaHong-Yan WangQian-Wen FanYue-Yue WangChao LiJing WangZi-Mu HuXue-Fu WangFeng-He LiMing-Ming LiuJuan JinChao ShiJia-Gen WenPublished in: Molecules (Basel, Switzerland) (2022)
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.
Keyphrases
- cell death
- cell cycle arrest
- drug induced
- oxidative stress
- flow cytometry
- nuclear factor
- diabetic rats
- induced apoptosis
- high glucose
- pi k akt
- endoplasmic reticulum stress
- toll like receptor
- risk assessment
- amino acid
- protein protein
- binding protein
- fluorescent probe
- emergency department
- inflammatory response
- adverse drug
- drug delivery
- nitric oxide
- multidrug resistant
- replacement therapy