“…SeMet supplementation significantly reduced aortic atherosclerotic plaque formation, improved vessel function, and decreased the inflammatory response in high fat diet fed apolipoprotein E deficient (ApoE –/– ) mice, highlighting the potential of SeMet supplementation in atherosclerosis therapy (Zhang et al., 2020). SeMet acted as an antioxidant to prevent cholestasis‐induced liver damage and inflammation (Brzački et al., 2019), and it also alleviated T‐2 toxin (type A trichothecenes)‐induced oxidative stress, inflammatory response, intestinal barrier damage, and kidney injury (Liu, Dong, et al., 2020; Liu, Yang, et al., 2020). SeMet and selenite both reduced 3,5‐dimethylaminophenol‐induced oxidative stress, DNA damage, and apoptosis in human urothelial cells, and SeMet at a concentration of 10 μmol/L exerted protecting effect equal to that of selenite at a concentration of 30 μmol/L (Erkekoglu et al., 2019).…”