“…These changes are quite obvious, as the increase of iNOS activity is mediated by the high content of inflammatory cytokines in the area of inflammation [36]. UC is characterized by destructive changes in CM, accompanied by increased content of MDA, protein and mRNA expressions of TNF-α [37], NF-κBp65 [38], IL-1β, IL-17 [39], IL-2, IL-4, IL-5 [40], increased activity of SOD and MPO [41], increased concentrations of prostaglandin E 2 and leukotriene B 4 , decreased total glutathione content [42], increased iNOS and COX-2 expression [43], as well as decreased activity of arginase due to bacterial lipopolysaccharides and flagellin admission, in addition to increased oxidative processes in the CM [44]. What is more, increased activity of iNOS under conditions of UC causes reduction of L-arginine concentration and arginase activity [45], indicating the redistribution of L-arginine utilization by NOS and arginase under conditions of inflammation.…”