6-Methoxyflavanones as Bitter Taste Receptor Blockers for hTAS2R39

被引:86
|
作者
Roland, Wibke S. U. [1 ]
Gouka, Robin J. [2 ]
Gruppen, Harry [1 ]
Driesse, Marianne [1 ]
van Buren, Leo [2 ]
Smit, Gerrit [1 ]
Vincken, Jean-Paul [1 ]
机构
[1] Wageningen Univ, Food Chem Lab, NL-6700 AP Wageningen, Netherlands
[2] Unilever R&D, Vlaardingen, Netherlands
来源
PLOS ONE | 2014年 / 9卷 / 04期
关键词
STRUCTURAL REQUIREMENTS; ACTIVATE; PEPTIDES; SUBUNITS;
D O I
10.1371/journal.pone.0094451
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many (dietary) bitter compounds, e. g. flavonoids, activate bitter receptor hTAS2R39 in cell-based assays. Several flavonoids, amongst which some flavanones, are known not to activate this receptor. As certain flavanones are known to mask bitter taste sensorially, flavanones might act as bitter receptor antagonists. Fourteen flavanones were investigated for their potential to reduce activation of hTAS2R39 by epicatechin gallate (ECG), one of the main bitter compounds occurring in green tea. Three flavanones showed inhibitory behavior towards the activation of hTAS2R39 by ECG: 49-fluoro-6-methoxyflavanone, 6,39-dimethoxyflavanone, and 6-methoxyflavanone (in order of decreasing potency). The 6-methoxyflavanones also inhibited activation of hTAS2R14 (another bitter receptor activated by ECG), though to a lesser extent. Dose-response curves of ECG at various concentrations of the full antagonist 49-fluoro-6-methoxyflavanone and wash-out experiments indicated reversible insurmountable antagonism. The same effect was observed for the structurally different agonist denatonium benzoate.
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页数:10
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