A 3.2 mM solution of 6-n-propyl-2-thiouracil (European Pharmacopoeia Reference Standard, Sigma Aldrich, Milano, Italy) was prepared by dissolving 0.5447 g/L in deionized water [11 (link)]. Respondents evaluated the bitter intensity of two identical samples (10 mL) using the gLMS, presented monadically in white plastic cups and coded with two different three-digit codes [7 (link)]. Participants were instructed to hold each sample in their mouth for 10 s, expectorate, and then wait 20 s before evaluating the bitterness intensity. In order to control for carry-over effects after the first evaluation, a break of 90 s was taken between the two evaluations. During this break, participants rinsed their mouth with water (30 s), had a cracker (30 s) then rinsed their mouth again. Participants were grouped according to their PROP status on the basis of arbitrary cut-offs reported in previous studies [63 (link),69 (link),70 (link)] corresponding to Non Taster (NT; gLMS ≤moderate, 17), Medium Taster (MT) and Super Taster (ST; gLMS ≥very strong, 53).
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