2007
DOI: 10.1096/fj.07-9591com
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The taste transduction channel TRPM5 is a locus for bitter‐sweet taste interactions

Abstract: Ordinary gustatory experiences, which are usually evoked by taste mixtures, are determined by multiple interactions between different taste stimuli. The most studied model for these gustatory interactions is the suppression of the responses to sweeteners by the prototype bitter compound quinine. Here we report that TRPM5, a cation channel involved in sweet taste transduction, is inhibited by quinine (EC(50)=50 microM at -50 mV) owing to a decrease in the maximal whole-cell TRPM5 conductance and an acceleration… Show more

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Cited by 78 publications
(61 citation statements)
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“…In contrast, Suc produced a feeble excitatory response when presented alone (Fig.3), but caused nonreciprocal inhibition of the excitatory responses of GRNs to the other plant chemicals (Figs4-6). One possible explanation for this latter case of non-reciprocal inhibition is that Suc directly antagonized the signaling pathways for AA, Glu and Ino (see Talavera et al, 2008).…”
Section: Mixture Suppression In the Peripheral Taste Systemmentioning
confidence: 99%
“…In contrast, Suc produced a feeble excitatory response when presented alone (Fig.3), but caused nonreciprocal inhibition of the excitatory responses of GRNs to the other plant chemicals (Figs4-6). One possible explanation for this latter case of non-reciprocal inhibition is that Suc directly antagonized the signaling pathways for AA, Glu and Ino (see Talavera et al, 2008).…”
Section: Mixture Suppression In the Peripheral Taste Systemmentioning
confidence: 99%
“…The similarities in sweet and bitter transduction have lead to considerable research regarding interactions between the two tastes; for review, see Margolskee (2002). Recent research has focussed on specific taste receptor cells and their role in sweet and bitter taste interactions, indicating peripheral gustatory integration (Talavera et al 2008).…”
Section: Introductionmentioning
confidence: 99%
“…The block of TRPM5 by quinine predicts that co-delivery of quinine with an agonist of the sweet receptors, which also act upstream of TRPM5, will blunt the sweet response. This is indeed what is observed, leading to the conclusion that TRPM5 is a locus for interaction between sweet and bitter tastes (Talavera et al 2008). In a directed high-throughput screen for specific blockers of TRPM5, the chemical triphenylphosphine oxide, TPPO, was identified (Palmer et al 2010).…”
Section: Pharmacologymentioning
confidence: 56%