The development of a specific inhibitor for bitter taste has been wide
ly required in the fields of taste physiology and pharmaceutical scien
ces, but no inhibitor has been available. We found that lipoproteins,
PA-LG composed of phosphatidic acid (PA) and p-lactoglobulin (LG) and
PA-LA composed of PA and cu-lactalbumin (LA) reversibly suppressed the
responses of the frog glossopharyngeal nerve to the bitter substances
. The frog tongue was treated with PA-LG solution for 10 min and then
stimulated by a stimulus dissolved in water. The responses to the bitt
er substances such as quinine hydrochloride, papaverine hydrochloride,
caffeine and L-leucine were completely suppressed by PA-LG, while tho
se to the salt type bitter substances such as CsCl, MgCl2 and tetraeth
ylammonium chloride were not suppressed. The responses to NaCl, galact
ose, acetic acid and L-alanine were unchanged or only slightly increas
ed. The results suggested that binding of PA-LG to the hydrophobic reg
ion of the receptor membranes leads to suppression of the responses to
the bitter substances. It was pointed out that PA-LG is useful not on
ly for elucidating the receptor mechanisms of bitter substances, but a
lso can be safely used to mask the bitter taste of foods and drugs, si
nce PA, LG and LA are prepared from foods (soybean and milk).