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Dipeptidylpeptidase IV hydrolyses gastric inhibitory polypeptide, glucagonlike peptide1(736)amide, peptide histidine methionine and is responsible for their degradation in human serum

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In addition, experimental studies have shown that the elevation of GSH can inhibit the activation of hepatic stellate cells [33], which is a key driving factor for extracellular matrix deposition and fibrosis, thereby preventing the progression of liver fibrosis [34]