Data #Temsirolimus molecular weight randurls[1|1|,|CHEM1|]# analysis and statistics Error bars shown on graphs and in Tables are standard deviations. Statistical signficance was tested by ANOVA using the Tukey-Kramer post-test for multiple comparisons. Results We recently reported that the xanthine oxidase (XO) enzyme pathway is activated in response to EPEC and STEC infection [23]. Infection with these pathogens triggers a release of nucleotides and nucleosides into the gut lumen, and XO itself is also released into the lumen of the intestine as a result of damage inflicted by these pathogens. XO catalyzes the conversion of hypoxanthine to xanthine

and xanthine to uric acid, with both steps creating one molecule of hydrogen peroxide. As previously reported by Wagner for oxidant molecules generated from neutrophils [22], XO-generated H2O2 increases the production of Stx from STEC strains [23].

Since H2O2 is known to be able to damage intestinal epithelia [32, 33], we thought this would be a relevant model to test whether selleck products zinc or other metals could protect against oxidant damage, since zinc has been reported to reported to help restore intestinal barrier function following other insults [34]. We used T84 cells grown to confluency in polarized monolayers in Transwell inserts as previously reported [28]. We measured trans-epithelial electrical resistance (TER), an index of intestinal barrier function, as well as H2O2-induced 3-mercaptopyruvate sulfurtransferase translocation of Stx2 from apical to basolateral chambers. Figure  1 shows the effects of H2O2 on TER and Stx2 translocation. H2O2 damages tight junctions and increases permeability via the paracellular pathway [35]. Figure  1A shows that H2O2 has concentration-dependent and time-dependent effects on TER in the T84 monolayers. 1 mM H2O2 paradoxically

increased TER slightly, but 2 mM H2O2 caused a moderate drop in TER. H2O2 at 3 mM and above damaged the monolayers severely, with TER falling to ~100 Ω, which is equivalent to that of the Transwell filters alone without any cells. Figure  1B shows that H2O2 also had a concentration dependent effect on Stx2 translocation, with Stx2 translocation detectable at H2O2 concentrations of 3 mM or higher. The inset in Figure  1B shows that H2O2 was also able to trigger a flux of fluorescein-labeled dextran-4000 across the monolayer, and that the monolayer damage could be prevented by the addition of catalase. Figure  1C shows that zinc could increase the TER in T84 cells not subjected to hydrogen peroxide or any other noxious stimulus, and Figure  1D shows that zinc could protect against the drop in TER induced by treatment with 2% dimethylsulfoxide (DMSO), at least at intermediate concentrations. Zinc acetate seemed to reduce the drop in TER (∆ TER) induced by 3 mM H2O2, although this protective effect did not reach statistical significance (Figure  1E). Figure  1F shows, however, that intermediate concentrations of zinc (0.1 to 0.