RT Journal Article SR Electronic T1 The Ceiling Effect of Pharmacological Postconditioning with the Phytoestrogen Genistein Is Reversed by the GSK3β Inhibitor SB 216763 [3-(2,4-Dichlorophenyl)-4(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione] through Mitochondrial ATP-Dependent Potassium Channel Opening JF Journal of Pharmacology and Experimental Therapeutics JO J Pharmacol Exp Ther FD American Society for Pharmacology and Experimental Therapeutics SP 1134 OP 1141 DO 10.1124/jpet.109.152587 VO 329 IS 3 A1 Nicolas Couvreur A1 Renaud Tissier A1 Sandrine Pons A1 Mourad Chenoune A1 Xavier Waintraub A1 Alain Berdeaux A1 Bijan Ghaleh YR 2009 UL http://jpet.aspetjournals.org/content/329/3/1134.abstract AB In the present study, we investigated the efficacy of pharmacological postconditioning induced by 17β-estradiol and the phytoestrogen, genistein, against myocardial infarction induced by increasing durations of coronary artery occlusion (CAO). Anesthetized rabbits underwent either 20-min (protocol A) or 30-min (protocol B) CAO, followed by 4 h of coronary artery reperfusion (CAR). Before CAR, they randomly received an intravenous injection of either vehicle (control), 100 or 1000 μg/kg genistein (Geni100 and Geni1000, respectively), or 100 μg/kg 17β-estradiol (17β-E100). In protocol A, infarct size was significantly reduced in Geni100 (n = 6), Geni1000 (n = 6), and 17β-E100 (n = 6) versus control (n = 9) (6 ± 2, 15 ± 4, and 11 ± 3 versus 35 ± 5%, respectively). In protocol B, none of these drugs reduced infarct size versus control. Western blots demonstrated an increase of Akt phosphorylation in the Geni100 and 17β-E100 hearts submitted to 20-min CAO but not to 30-min CAO. The selective GSK3β inhibitor SB 216763 (0.2 mg/kg) [3-(2,4)-dichlorophenyl)-4(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione] did not exhibit cardioprotection at this dose, but its administration restored the cardioprotective effect of genistein and 17β-estradiol with 30-min CAO. Administration of 5-hydroxydecanoate (5 mg/kg) abolished the cardioprotective effects of Geni100 and 17β-E100 alone with 20-min CAO and also those observed when combined to SB 216763 with 30-min CAO. Thus, pharmacological postconditioning with genistein and 17β-estradiol is limited by a “ceiling effect of protection” along with a loss of Akt phosphorylation. However, this ceiling effect is reversed by concomitant inhibition of GSK3β by SB 216763 through opening of mitochondrial ATP-dependent potassium channels. The American Society for Pharmacology and Experimental Therapeutics