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The supplement-drug interaction of quercetin with tamsulosin on vasorelaxation

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Abstract

The food supplement quercetin is used as self-medication for prostate disorders and is known to induce vasorelaxation. The drug tamsulosin is used in the treatment of benign prostatic hyperplasia. A major side effect of tamsulosin is orthostatic hypotension, mediated by vasorelaxation resulting from alpha1-adrenoceptor blockade. The overlapping profile prompted us to investigate the pharmacodynamic interaction of quercetin with tamsulosin. Since quercetin is extensively metabolized in the intestines and the liver, the metabolites quercetin-3-glucuronide and 4'O-methyl-quercetin were also examined. Vasorelaxation induced by the compounds was tested in rat mesenteric arteries (average diameter: 360+/-mum) constricted by the alpha1-adrenoceptor agonist phenylephrine. Tamsulosin (0.1nM) decreased phenylephrine sensitivity 17-fold (n=10). Quercetin (5, 10 and 20microM) also caused a decrease (2-, 4- and 6-fold respectively) of phenylephrine sensitivity, while 10microM of quercetin-3-glucuronide and 4'O-methyl-quercetin decreased this sensitivity (1.5- and 2-fold) only slightly (n=6). The combination of tamsulosin with quercetin or quercetin metabolites proved to be far more potent than the compounds in isolation. The combination of quercetin, quercetin-3-glucuronide or 4'O-methyl-quercetin with tamsulosin decreased the phenylephrine sensitivity approximately 200-, 35- and 150-fold (n=6). The strong pharmacodynamic interaction between the food supplement quercetin and tamsulosin underlines the potential of the impact of supplement-drug interactions that warrant more research.

    Research areas

  • Quercetin, Tamsulosin, Vasorelaxation, Orthostatic hypotension, Supplement-drug interaction, Pharmacodynamics, URINARY-TRACT SYMPTOMS, FLAVONOID QUERCETIN, ALPHA(1)-ADRENERGIC RECEPTORS, ELDERLY-PEOPLE, IN-VITRO, NUTRITIONAL-STATUS, HYDROGEN-PEROXIDE, BLOOD-PRESSURE, ARTERIES, RATS
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Details

Original languageEnglish
Pages (from-to)132-137
Number of pages6
JournalEuropean Journal of Pharmacology
Volume746
DOIs
Publication statusPublished - 5 Jan 2015