Antihypertensive and vasorelaxant effects of dihydrospinochalcone-A isolated from Lonchocarpus xuul Lundell by NO production: Computational and ex vivo approaches

作者：Avila Villarreal Gabriela; Hernandez Abreu Oswaldo; Hidalgo Figueroa Sergio; Navarrete Vazquez Gabriel; Escalante Erosa Fabiola; Pena Rodriguez Luis M; Villalobos Molina Rafael; Estrada Soto Samuel^*

来源：Phytomedicine, 2013, 20(14): 1241-1246.

DOI：10.1016/j.phymed.2013.06.011

• Antihypertensive
• Dihydrospinochalcone-A
• Lonchocarpus xuul
• Docking
• Isocordoin
• Nitric oxide
• Vasorelaxant

Current work was conducted to evaluate the vasorelaxant effect of dihydrospinochalcone-A (1) and isocordoin (2), compounds type chalcone isolated from Lonchocarpus xuul, an endemic tree of the Yucatan Peninsula, Mexico. Compounds 1 and 2 were found to induce significant relaxant effect in a concentration-dependent manner on aortic rat rings pre-contracted with noradrenaline (NA, 0.1 mu M). Compound 1 was the most active and its effect was endothelium-dependent (Emax = 79.67% and EC50 = 21.46 mu M with endothelium and Emax = 23.58% and EC50 = 91.8 mu M without endothelium, respectively). The functional mechanism of action for 1 was elucidated. Pre-incubation with L-NAME (unspecific nitric oxide synthase inhibitor), indomethacin (unspecific COX inhibitor), ODQ (soluble guanylyl cyclase inhibitor), atropine (cholinergic receptor antagonist), TEA (unspecific potassium channel blacker) reduced relaxations induced by 1. Oral administration of 50 mg/kg of compound 1 exhibited significant decrease in diastolic and systolic blood pressure in SHR rats. The heart rate was not modified. Compound 1 was docked with a crystal structure of eNOS. Dihydrospinochalcone-A showed calculated affinity with eNOS in the C1 binding pockets, near the catalytic site; Trp449, Trp447 and His373 through aromatic and pi-pi interactions, also His463 and Arg367 are the residues that make hydrogen bonds with the carbonyl and hydroxyl groups.
In conclusion, dihydrospinochalcone-A induces a significant antihypertensive effect due to its direct vasorelaxant action on rat aorta rings, through NO/sCG/PKG pathway and potassium channel opening.

• 出版日期2013-11-15