Chlorhexidine, a bis-cationic biguanide antiseptic, greatly reduces the per
ceived intensity of the salty prototype sodium chloride and may prove to be
an important probe of mechanisms that underlie the human salty taste quali
ty, Chlorhexidine, which tastes bitter, also reduces quinine hydrochloride
taste intensity, but neither sweet sucrose nor sour citric acid is affected
. Perceptual intensity rating and quality identification were measured for
human subjects before and for 30 min following treatment with 1.34 mM chlor
hexidine gluconate. In one experiment, test stimuli were the taste-quality
prototypes; in a second experiment, stimuli were series of sodium, halide a
nd sulfate salts. Experiment 1 showed a single 3-min chlorhexidine treatmen
t resulted in reductions in taste intensity that persisted for at least 30
min. Experiment 2 showed a single 2-min chlorhexidine treatment reduced per
ceptual intensities of halide and sulfate salts except those with divalent
cations. Chlorhexidine impaired identification of the salty quality and pro
duced a bitter quality in nonbitter salts and impaired identification of th
e bitter quality of quinine, but not bitter salts. The specific effect of c
hlorhexidine on the bitterness of quinine suggests it may bind to the same
receptor as quinine. The ability of chlorhexidine to specifically disrupt s
altiness of a wide range of salts is consistent with proposed peripheral tr
ansduction mechanisms for the salty quality that involve transepithelial io
n transport. (C) 2001 Elsevier Science Inc. All rights reserved.