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. Author manuscript; available in PMC: 2012 Jul 9.
Published in final edited form as: Glia. 2008 Jan 1;56(1):78–88. doi: 10.1002/glia.20596

Figure 7.

Figure 7

Effects of 50 mM EtOH or 100 μM AA on the BBB functional assays (A) Changes in TEER, (B) 4 kDa dextran permeability, and (C) monocyte migration across the BBB. Prior to TEER, permeability or migration assay, cell monolayers were treated with EtOH for 48 hr or with AA for 2 hr in the presence or absence of specific inhibitor. Results were expressed as percent of controls or apparent permeability coefficient “P” (± SEM; n = 3). Respective inhibitor alone did not change the BBB functional integrity of the basal controls.