“…Current research supports several earlier reports that have shown that LPS induces hepatic damage, and therefore increases the concentrations of the aminotransferases (ALT, AST, ALP, and GGT) [11,[28][29][30][31][32][33]. The hepatic enzymes are cytoplasmic, and alteration in the membrane permeability will cause dysfunction and damaged structural integrity of hepatocytes and the aminotransferases to leak to the bloodstream, thereby resulting in an increase of the aminotransferases in the plasma of the male and female rat models, characterized by viral hepatitis, diabetes, heart failure, bile duct problems, haemorrhage, inflammation, cardiac, muscular, biliary, and injury, and microabscess formation, activation of the transcription factor nuclear factor-kappa B, and many inflammatory genes [11,27,28,30,33,[34][35][36][37].…”