To determine whether the idiosyncratic distribution of transduction me
chanisms for bitter tastants in rat taste receptor cells (TRCs) could
be inferred from the neural activity they evoke, single neuron respons
es to ten bitter-tasting compounds were recorded from rat glossopharyn
geal (n = 30) and chorda tympani (n = 22) neurons. Responses to severa
l 'bitter' alkaloids were obtained: 10 mM quinine-HCl, 50 mM caffeine,
and 1 mM each nicotine, yohimbine, and strychnine, plus a number of n
on-alkaloid bitter-tasting compounds: 0.1 M KCl, 0.01 M MgCl2, and 1 m
M each phenylthiocarbamide (PTC), L-tyrosine, and denatonium benzoate.
To obtain some distinctions with other stimuli NaCl(0.1 M), HCl (pH 2
.0), and capsaicin (10 mu M) were also tested. It was found that indiv
idual neurons in both glossopharyngeal and chorda tympani nerves diffe
red in their relative sensitivities to the various bitter stimuli. To
determine relationships among these stimuli, the differences in the ev
oked responses between each stimulus pair were summarized in a multi-d
imensional scaling space. In these analyses neither nerve showed any o
bvious similarity between the placements of quinine and the other bitt
er stimuli. Such data suggest that first-order gustatory neurons can d
iscriminate among the above bitter stimuli, For glossopharyngeal neuro
ns, some similarity to quinine was found only for nicotine and denaton
ium, and for chorda tympani neurons, some similarity to quinine was fo
und only for KCl and MgCl2. Of the bitter compounds tested, quinine ev
oked the greatest response from glossopharyngeal neurons. We propose t
his arises because quinine can activate TRCs by more transduction mech
anisms than other bitter stimuli. The results from these studies were
summarized in a qualitative model for the coding of bitter tastants wh
ere the variety of transduction mechanisms for bitters are distributed
among various TRCs to account for the heterogeneous responses among t
he neurons. (C) 1997 Elsevier Science B.V.