Abstract

The mechanism underlying the vasodilator effect of the flavonoid floranol was studied in rat small mesenteric arteries. Floranol produced a concentration-dependent vasorelaxant effect in endothelium-containing and endothelium-denuded vessels pre-contracted with phenylephrine, which was more potent in endothelium-intact vessels. In endothelium-intact mesenteric arteries, l-NAME but not indomethacin produced a shift to the right in the vasorelaxant effect of floranol. In endothelium-denuded vessels TEA and BaCl2 did not change the floranol-induced vasorelaxation. When endothelium-denuded vessels were pre-contracted with 50 mM KCl, floranol induced a vasorelaxant effect comparable with phenylephrine pre-contracted vessels. We conclude that floranol is a new vasodilator compound in rat small mesenteric arteries. Part of this effect is dependent on endothelial nitric oxide (NO) and part is dependent on the inhibition of voltage-dependent calcium channels in the smooth muscle cells.

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