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   <subfield code="a">Effect of phenylephrine and endothelium on vasomotion in rat aorta involves potassium uptake</subfield>
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   <subfield code="c">[Javier Palacios, José Vega, Adrián Paredes, Fredi Cifuentes]</subfield>
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   <subfield code="a">Vasomotion is defined as the rhythmic contractions in blood vessels, consisting of two components: vasoconstriction and oscillations of the plasma membrane potential. To determine whether vasomotion is associated with changes in K+ uptake, we measured the effect of phenylephrine (PE) and acetylcholine (ACh) on the K+ uptake and vascular reactivity in rat aortic rings. We found that the incubation of aortic rings with 10−7M PE (210±28mg maximum amplitude), and 10−6M ACh (177±6mg maximum amplitude) produced the highest rhythmic contractions. Both 10−7M PE and 10−6M ACh significantly increased K+ uptake in endothelium-intact aorta versus control (121% PE, 117% ACh). Removal of the endothelium blunted rhythmic contractions and decreased K+ uptake in presence of vasoactive substances (88% PE, 81% ACh). The inhibition of nitric oxide synthase with 10−4M l-NNA significantly reduced the rhythmic contractions, and it was reversed in the presence of 10−8M sodium nitroprusside (SNP; a nitric oxide donor). Also, we found that 10−4M l-NNA significantly decreased the effect of 10−7M PE on K+ uptake in aortic rings (104% PE+l-NNA vs. control). The incubation of endothelium-denuded rings with 10−8M SNP significantly increased the K+ uptake (116% SNP vs. control), similar to those observed in the presence of 10−6 M ACh. The inhibition of protein kinase G with KT-5823 blocked SNP-mediated increase in K+ uptake. In conclusion, these data suggest that a certain range of K+ uptake is necessary to induce the rhythmic contractions in response to vasoactive substances.</subfield>
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