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A study observed that amino acids containing selenium such as selenocysteine and its derivative selenocystine, Alpha-methyl selenocysteine [(αMe)Sec] could improve DSS-triggered oxidative stress and intestinal inflammation in mice (39)

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suggested that QE coordinately activated autophagy and combated exosomes release by restoring lysosome function, and further mitigated ethanol-induced liver damage ( 2.7.1.4 Effects of QE on liver fibrosis In an experiment conducted by Hernandez et al., treatment with QE prevented liver injury in an animal model of CCl 4 -induced cirrhosis by increasing CB2 expression, reducing CB1 expression, promoting apoptosis of HSC and decreasing the number of activated HSCs (Li et al., 2016)