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Quercetin: A Treatment for Hypertension?—A Review of Efficacy and Mechanisms

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Department of Exercise and Sport Science, University of Utah, HPER North, 250 South 1850 East, SLC UT, 84112, USA
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Department of Nutrition, University of Utah, HPER North, 250 South 1850 East, SLC UT 84112, USA
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Author to whom correspondence should be addressed.
Pharmaceuticals 2010, 3(1), 237-250; https://doi.org/10.3390/ph3010237
Received: 8 December 2009 / Revised: 12 January 2010 / Accepted: 14 January 2010 / Published: 19 January 2010
(This article belongs to the Special Issue Antihypertensive Drugs)
Quercetin is a polyphenolic flavonoid. Common sources in the diet are apples, onions, berries, and red wine. Epidemiological studies have found an inverse relationship between dietary quercetin intake and cardiovascular disease. This has led to in vitro, in vivo, and clinical research to determine the mechanism by which quercetin exerts cardioprotective effects. Recent studies have found a reduction in blood pressure when hypertensive (>140 mm Hg systolic and >90 mm Hg diastolic) animals and humans are supplemented with quercetin. Proposed mechanisms for the antihypertensive effect of quercetin include decreased oxidative stress, inhibition of angiotensin converting enzyme activity, improved endothelial function, direct action on the vascular smooth muscle, and/or modulation in cell signaling and gene expression. Although in vitro and in vivo evidence exists to support and refute each possibility, it is likely that quercetin influences multiple targets via a combination of known and as yet undiscovered mechanisms. The purpose of this review is to examine the mechanisms whereby quercetin might reduce blood pressure in hypertensive individuals. View Full-Text
Keywords: quercetin; hypertension; angiotensin converting enzyme; endothelial function; antioxidants quercetin; hypertension; angiotensin converting enzyme; endothelial function; antioxidants
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Larson, A.J.; Symons, J.D.; Jalili, T. Quercetin: A Treatment for Hypertension?—A Review of Efficacy and Mechanisms. Pharmaceuticals 2010, 3, 237-250.

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