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. 2017 Oct 25;595(22):6869–6885. doi: 10.1113/JP275052

Figure 5. TRPV4 stimulation rapidly and dramatically decreases the impedance of HrMVEC monolayers and increases the in vivo permeability of retinal blood vessels.

Figure 5

The ‘normalized monolayer impedance’ is derived by dividing the impedance value by the value at a reference time point. A, 2.5 nm (red), 5 nm (brown) and 10 nm (green trace) GSK101 dose‐dependently decrease the resistance of HrMVEC monolayers. B, cumulative data for the experiments shown in A (N = 3). C, HC‐06 (orange) inhibits 10 nm GSK101‐induced decreases in monolayer resistance (brown trace) (N = 3). D, averaged data from C. * P < 0.05, ** P < 0.001, **** P < 0.00001, paired t test. E, systemic injection of GSK101 increases the retinal extravasation of Evans Blue 2 h after dye injection, indicated by increased absorbance signal in WT (grey bar) compared to Trpv4−/− retinas (red bar). The dots represent individual retinas; values are normalized to control values of dye‐exposed retinas in the absence of the TRPV4 agonist. Retinal extravasation was measured 2 and 24 h after GSK101 treatment. F, cumulative data for three independent experiments from WT (black bars) and Trpv4−/− retinas measured 2 and 24 h after GSK101 treatment. * P = 0.033; N.S., P > 0.05; one‐way ANOVA. Mean ± SEM. [Color figure can be viewed at wileyonlinelibrary.com]