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The surge of flavonoids as novel, fine regulators of cardiovascular Cav channels

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 796, Issue -, Pages 158-174

Publisher

ELSEVIER
DOI: 10.1016/j.ejphar.2016.12.033

Keywords

Flavonoid; Quercetin; Ca(v)1.2 channel; Cardiovascular system; Patch-clamp; Molecular docking

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Ion channels underlie a wide variety of physiological processes that involve rapid changes in cell dynamics, such as cardiac and vascular smooth muscle contraction. Overexpression or dysfunction of these membrane proteins are the basis of many cardiovascular diseases that represent the leading cause of morbidity and mortality for human beings. In the last few years, flavonoids, widely distributed in the plant kingdom, have attracted the interest of many laboratories as an emerging class of fine ion, in particular Ca-v, channels modulators. Pieces of in vitro evidence for direct as well as indirect effects exerted by various flavonoids on ion channel currents are now accumulating in the scientific literature. This activity may be responsible, at least in part, for the beneficial and protective effects of dietary flavonoids toward cardiovascular diseases highlighted in several epidemiological studies. Here we examine numerous studies aimed at analysing this feature of flavonoids, focusing on the mechanisms that promote their sometimes controversial activities at cardiovascular Ca-v channels. New methodological approaches, such as molecular modelling and docking to Ca(v)1.2 channel alpha(1c) subunit, used to elucidate flavonoids intrinsic mechanism of action, are introduced. Moreover, flavonoid-membrane interaction, bioavailability, and antioxidant activity are taken into account and discussed.

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