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. 2013 Jan 24;168(4):794–806. doi: 10.1111/j.1476-5381.2012.02189.x

Figure 4.

Figure 4

(A) Concentration–response curves to the selective EP1/EP3 receptor agonist sulprostone in endothelium-intact guinea pig aorta after treatment with the selective EP3 receptor antagonist ONO-AE5-599 (O599). (B) Concentration–response curves to PGE2 in rat tracheal segments pre-contracted with 0.3 μM CCh and treated with the EP4 receptor antagonist ONO-AE3-208 (O208). All experiments were performed in the presence of 3 μM indomethacin and in panel A; 10 nM of the EP1 receptor antagonist ONO-8130 was also added. Data represent mean ± SEM (n = 4–8).