SciELO - Scientific Electronic Library Online

 
vol.56 issue4ESTUDIO DESCRIPTIVO SOBRE TABAQUISMO EN LA COMUNIDAD ESTUDIANTIL DE LA UNIVERSIDAD DE MANIZALES. 2007 author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Revista de la Facultad de Medicina

Print version ISSN 0120-0011

Abstract

CORREA-HERNANDEZ, Sofía Ximena et al. Vasodilator profile of flavonoid and phenylbutanoid compounds isolated from Croton schiedeanus Schlecht. rev.fac.med. [online]. 2008, vol.56, n.4, pp.291-301. ISSN 0120-0011.

Background. Croton schiedeanus Schlecht (Euphorbiaceae), specie is used in Colombian folk medicine in hypertension treatment. Objective. To assess the vasorelaxant effect of the flavonoid compounds: 3-O-methyl-quercetin, 3,7-di-O-methylquercetin, and 3,3',4',7-tetra-O-methylquercetin, and the phenylbutanoids compounds: (2S)-7,9-dimethoxyrhododendrol, (2S)-2-acetoxy-7,9-dimetho-xyrho-dodendrol, (2S)-2,8-diacetatoxy-7,9-dimethoxyrho-dodendrol in isolated aortic rings of Wistar rats. Materials and methods. These compounds were evaluated in phenylephrine (PE, 1 µM) and KCl (80 mM) precontracted aortic rings. In order to examine possible interactions related with: endothelium, nitric oxide (NO), guanylyl ciclasa, prostanoid or ATP dependent potassium (K+ATP) channels, the compounds with greater relaxant effect: 3-O-methylquercetin, and 3,7-di-O-methylquer-cetin, were assessed in phenylephrine precontracted rings in presence or absence of: endothelium, L-NAME (G -nitro-L-Arginine-Methyl Ester, 100 µM), ODQ (1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one, 1 µM), sodium meclofenamate (10 µM) or glibenclamide (1 µM). Results. Whereas phenylbutanoid compounds did not shown significant relaxant properties, 3-O-methylquercetin and 3,7-di-O-methyl-quercetin displayed important vasodilator responses with IC50 of 2.5 and 4.9 µM against phenylephrine respectively. ODQ and L-NAME effectively displaced to the right the dose-response curves of these compounds, especially in the case of 3-O-methylquercetin (IC50 ratio: 7.4 and 3.8) whereas glibenclamide did not and meclofenamate only slightly. Conclusion. 3-O-methylquercetin and 3,7-di-O-methylquercetin, flavonoid compounds isolated from Croton schiedeanus play important vasorelaxant effects related to the NO/cyclic GMP pathway. These results support the etnobotanical use of Croton schiedeanus.

Keywords : Euphorbiaceae; Rhododendrol; 3-O-Methylquercetin; 3,7-Di-O-methylquer-cetin; Nitric Oxide; vasodilator Agents.

        · abstract in Spanish     · text in English     · English ( pdf )