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. 2009 Jan 28;296(4):C801–C810. doi: 10.1152/ajpcell.00620.2008

Fig. 5.

Fig. 5.

Changes in paracellular permeability in control and polyamine-deficient IEC-6 cells with or without challenge with H2O2. A: basal levels of paracellular permeability. After cells were grown in control cultures or cultures containing DFMO or DFMO + SPD for 4 days, they then were trypsinized, plated at confluent density on the insert, and maintained under the same culture conditions for an additional 48 h. Membrane-impermeable tracer molecule, [14C]mannitol, was added to the insert medium, and the entire basal medium was collected 2 h thereafter for paracellular tracer flux assays. Values are means ± SE of data from 6 samples. *P < 0.05 compared with control cells and cells treated with DFMO + SPD. B: paracellular permeability in controls (a) and polyamine-deficient cells (b) after challenge with different concentrations of H2O2 for 3 h. After cells were treated with H2O2 for 1 h, [14C]mannitol was added to the insert medium, and levels of [14C]mannitol were measured 2 h thereafter. Values are means ± SE of data from 6 samples. *P < 0.05 compared with control cells.