Show simple item record

Ouabain treatment changes the role of endothelial factors in rat resistance arteries

dc.contributor.authorPadilha, A
dc.contributor.authorPecanha, FM
dc.contributor.authorVassallo, DV
dc.contributor.authorAlonso, MJ
dc.contributor.authorSalaices, M
dc.date.accessioned2010-02-17T09:47:19Z
dc.date.available2010-02-17T09:47:19Z
dc.date.issued2008-12-14
dc.identifier.citationEur J Pharmacol. 2008 Dec 14;600(1-3):110-6es
dc.identifier.urihttp://hdl.handle.net/10115/3292
dc.description.abstractThis study investigates the participation of the endothelial factors in the ¿ adrenoceptor contractile responses in mesenteric resistance arteries from 15 days ouabain-treated (25 ¿g/kg/day) and untreated rats. Ouabain treatment increased blood pressure and heart rate without changing the contractile response to phenylephrine (3 nM¿30 ¿M). Endothelium removal or NG-nitro-L-arginine methyl ester (L-NAME, 100 ¿M), increased the responses to phenylephrine. The endothelial modulation was similar in both rat groups, but the L-NAME effects were bigger in arteries from ouabain-treated rats. However, the endothelial NOS expression and the relaxation to acetylcholine (0.1 nM¿10 ¿M) remained unaltered after ouabain treatment. The coincubation with L-NAME and indomethacin (100 ¿M) leftward shifted the concentration¿response curves to phenylephrine in arteries from untreated rats similarly to the displacement after incubation only with L-NAME. However, in mesenteric arteries from treated rats, the co-incubation with indomethacin and L-NAME did not alter the response to phenylephrine. The addition of the inhibitor of calcium activated potassium channels tetraethylammonium (2 mM) further leftward shifted the phenylephrine curves only in arteries from untreated rats. Cyclooxygenase-2 (COX-2) expression was greater in vessels from ouabaintreated rats. In conclusion, the chronic ouabain treatment for 15 days modified the participation of endothelial factors in response to phenylephrine in mesenteric resistance arteries, by increasing the release of NO and prostanoids and impairment the endothelium-derived hyperpolarizing factor (EDHF) release. This was accompanied by an increased COX-2 expression. Although this balance avoids changes in the phenylephrine concentration¿response curves, these vascular changes might contribute to maintain the ouabain-induced hypertension.es
dc.language.isoenes
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectBiología y Biomedicinaes
dc.titleOuabain treatment changes the role of endothelial factors in rat resistance arterieses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1016/j.ejphar.2008.10.023es
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.subject.unesco2411.03 Fisiología Cardiovasculares
dc.subject.unesco3209.90 Farmacología Experimentales
dc.description.departamentoCiencias de la Salud III


Files in this item

This item appears in the following Collection(s)

Show simple item record

Atribución-NoComercial-SinDerivadas 3.0 EspañaExcept where otherwise noted, this item's license is described as Atribución-NoComercial-SinDerivadas 3.0 España