Importantly, decreased Y198- and Y250-nitration was visualized by re-probing the blots with 3A11C6 anti-nitroY198-HGF and 6B82C3 anti-nitroY250-HGF-specific mAbs, respectively (Figure 1b,c, first rows)
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Supporting may also be the BPC 157-induced decrease of the inflammatory mediators, leukotriene B4 (LTB4), thromboxane B2 (TXB2), and myeloperoxidase (MPO), in both serum and inflamed tissue [40], largely implicated in heparin-induced platelet activation, the adhesion of leukocytes to the endothelium and concomitant increase in vascular permeability [41], prolongation of the bleeding time [42] while low-molecular-weight heparin enoxaparin causes systemic MPO activation [43]
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