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. 2019 Jun 5;317(2):C375–C389. doi: 10.1152/ajpcell.00444.2018

Fig. 11.

Fig. 11.

Inhibition of cation channel activity in Müller glia by fluoxetine (Fluox) treatment. Primary, purified cultures of Müller glia were exposed to ambient (Amb) or elevated (Elev) pressure for 4 h, in the presence of vehicle or 100 µM fluoxetine. A: representative heat map showing the fluorescent signal of Thallos dye in Müller glia from each condition. Images were taken after the addition of thallium. B: line graphs displaying the normalized fluorescence intensity of Thallos dyes over time for each condition. Student’s t-test was used to analyze statistical significance. C: box plots of the average fluorescence intensity following the addition of thallium compared between each condition. One-way ANOVA with pairwise comparison by Dunn’s method was used to analyze statistical significance. n(Amb) = 5 cells; n(Elev) = 12; n(Amb+Fluox) = 28; n(Elev+Fluox) = 22. *P < 0.05.