Why the study?
Does fenoldopam alter blood pressure, sodium excretion, and renal hemodynamics in healthy volunteers, and are these effects modulated by metoclopramide?
Does fenoldopam alter blood pressure, sodium excretion, and renal hemodynamics in healthy volunteers, and are these effects modulated by metoclopramide?
Fenoldopam induces systemic and renal vasodilation and natriuresis via direct stimulation of DA1 receptors, which can be blunted by dopamine antagonists like metoclopramide.
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Supports DA1-mediated renal effects in healthy subjects; leaves open translation to patients with disease.
The effects of fenoldopam (FD), a selective dopamine-1 (DA1) agonist in doses from 0.05 to 0.50 micrograms/kg/min and of the aselective dopamine antagonist metoclopramide (MCP) on blood pressure (BP), sodium excretion and renal hemodynamics were investigated in 10 healthy volunteers. During FD infusion the diastolic BP fell 9 mm Hg with a rise in heart rate. During combined infusion of FD and MCP no changes in BP occurred. Effective renal plasma flow rose for all doses of FD with a maximal increase of 36% and was not influenced by MCP infusion. Glomerular filtration rate remained unchanged. FD induced an increase in sodium and calcium excretion compared to placebo study, which was abolished by MCP. A marked rise of plasma renin activity during FD infusion was noted, blunted by MCP. MCP induced a marked increase of aldosterone, sustained, but blunted, during subsequent FD infusion, suggesting a DA1-mediated influence on aldosterone secretion. During infusion of FD alone, an increased urinary dopamine excretion was observed. We conclude that FD induces: (1) systemic and renal vasodilation and (2) natriuresis by direct stimulation of DA1 receptors in the proximal tubule, which is (partially) counteracted by a rise of plasma renin activity and subsequently of aldosterone.
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Girbes et al. (2008) studied this question.
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