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. 2012 Oct 8;7(10):e46735. doi: 10.1371/journal.pone.0046735

Figure 4. Histograms showing EDH evoked by SLIGRL (20 µM) in rat MCAs that are able to synthesise NO but treated with the TP receptor agonist, U46619 (50–100 nM).

Figure 4

Also shown is the effect of the HMG-CoA reductase inhibitor simvastatin at either 100 nM (A) or 1 µM (B) on EDH and the effect of blocking KCa3.1 alone (TRAM-34, 1 µM), in the subsequent presence of blockade of both KCa2.3 (apamin 100 nM) and KCa3.1 as well as the combined of blockade of KCa1.1 (iberiotoxin 100 nM), K­Ca2.3 and KCa3.1. *P<0.05 indicates a significant difference from control using one way ANOVA with Tukey’s post-test, n = 4–7. φP<0.05 indicates a significant difference from simvastatin (100 nM or 1 µM) as determined by one-way ANOVA with Tukey’s post-test, n = 4–7.