The quercetin metabolite 4-methylcatechol causes vasodilation via voltage-gated potassium (K V ) channels

• Published in: Food & function 2024-11, Vol.15 (22), p.11047-11059
• Main Authors: Dias, Patrícia, Salam, Rudy, Pourová, Jana, Vopršalová, Marie, Konečný, Lukáš, Jirkovský, Eduard, Duintjer Tebbens, Jurjen, Mladěnka, Přemysl
• Format: Article
• Language: English
• Subjects: Adenosine kinase; Adenosine monophosphate; Animals; Aorta; Aorta - drug effects; Aorta - metabolism; Calcium channels; Calcium channels (L-type); Calcium channels (voltage-gated); Calcium ions; Catechols - pharmacology; Channel gating; Cyclic AMP; Cyclic nucleotides; Guanylate cyclase; Hydrogen bonding; Hydrophobicity; Intestinal microflora; Isometric; Kinases; Male; Metabolites; Molecular Docking Simulation; Nucleotides; Phenolic compounds; Phenols; Polyphenols; Potassium; Potassium channels (voltage-gated); Potassium Channels, Voltage-Gated - metabolism; Protein kinase G; Quercetin; Quercetin - pharmacology; Rats; Rats, Wistar; Vasodilation; Vasodilation - drug effects; Vasodilator Agents - pharmacology
• ISSN: 2042-6496; 2042-650X; 2042-650X
• DOI: 10.1039/d3fo04672a

Dietary polyphenols have been associated with many beneficial cardiovascular effects. However, these effects are rather attributed to small phenolic metabolites formed by the gut microbiota, which reach sufficient concentrations in systemic circulation. 4-Methylcatechol (4-MC) is one such metabolite. As it is shown to possess considerable vasorelaxant effects, this study aimed to unravel its mechanism of action. To this end, experimental and approaches were employed. In the first step, isometric tension recordings were performed on rat aortic rings. 4-MC potentiated the effect of cyclic nucleotides, but the effect was not mediated by either soluble guanylyl cyclase (sGC), modification of cyclic adenosine monophosphate levels, or protein kinase G. Hence, downstream targets such as calcium or potassium channels were considered. Inhibition of voltage-gated K channels (K ) markedly decreased the effect of 4-MC, and vasodilation was partly decreased by inhibition of the K 7 isoform. Contrarily, other types of K channels or L-type Ca channels were not involved. reverse docking confirmed that 4-MC binds to K 7.4 through hydrogen bonding and hydrophobic interactions. In particular, it interacts with two crucial residues for K 7.4 activation: Trp242 and Phe246. In summary, our findings suggested that 4-MC exerts vasorelaxation by opening K channels with the involvement of K 7.4.