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. 2019 Feb 6;10:55. doi: 10.3389/fphys.2019.00055

Table 1.

Effects of the inhibitors of PI3K LY-294002 (3 μM), ERK-MAPK kinase PD-98059 (3 μM) and PKC GF-109203X (0.1 μM) on the sensitivity and maximal responses of the CaCl2 concentration-response curves in mesenteric arteries stimulated by PE (10 μM) in a Ca2+-free medium.

[Ca2+]i (F340/F380) Tension (Nm-1)


pEC50 Emax n pEC50 Emax n
Control 3.77 ± 0.06 0.34 ± 0.04 7 4.12 ± 0.09 4.73 ± 0.47 7
+ LY-294002 3.86 ± 0.04 0.25 ± 0.03 7 3.79 ± 0.09∗∗ 4.81 ± 0.61 7
Control 3.85 ± 0.08 0.42 ± 0.06 7 3.78 ± 0.06 4.36 ± 0.33 7
+ PD-98059 3.71 ± 0.17 0.23 ± 0.06∗∗∗ 7 3.73 ± 0.24 4.24 ± 0.32 7
Control 3.96 ± 0.10 0.33 ± 0.04 8 3.91 ± 0.12 5.97 ± 0.63 8
+ GF-109203X 3.90 ± 0.13 0.25 ± 0.04 8 3.93 ± 0.14 4.81 ± 0.69∗∗ 8

Data are means ± SEM; “n” number of arteries (one per animal) from Wistar rats. Results are expressed as absolute values, as the increases in the intracellular Ca2+ concentration [Ca2+]i (ratio F340/F380) and tension (Nm-1) elicited by PE or CaCl2. pEC50 is – log(EC50), EC50 being the concentration of agonist giving 50% of the maximum effect (Emax). Significant differences were analyzed by paired Student’s t-test. P < 0.05; ∗∗P < 0.01; ∗∗∗P < 0.001 vs. control.