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. Author manuscript; available in PMC: 2017 Sep 1.
Published in final edited form as: Vascul Pharmacol. 2016 May 31;84:47–54. doi: 10.1016/j.vph.2016.05.015

Figure 3. AT1 antagonist inhibits Ang II priming of PGE2.

Figure 3

(A) Representative wire myography trace of femoral arterial rings primed with 1 nM Ang II, followed by addition of 100 nM PGE2. (B) Representative trace of femoral artery with 30 minutes pretreatment with 1 μM losartan followed by addition of 1 nM Ang II priming of 100 nM PGE2. (C) Comparison between femoral arterial ring responses to 100 nM PGE2 with and without 1 nM Ang II priming, as well as with priming in the presence of an AT1 (losartan) or AT2 antagonist (PD123319) (N = 5). (D) Competition binding in wildtype mouse kidney membranes; displacement of [3H]PGE2 by the EP3 agonist sulprostone, losartan, and PD123319. Graph is normalized to competition binding with cold PGE2. (N = 3). * = P < 0.05