It is probable that there is a diversity of mechanisms involved in the
transduction of bitter taste. One of these mechanisms uses the second
messengers, inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DA
G). Partial membrane preparations from circumvallate and foliate taste
regions of mice tongues responded to the addition of known bitter tas
te stimuli by increasing the amount of inositol phosphates produced af
ter 30 s incubation. Addition of both the bitter stimulus, sucrose oct
aacetate and the G-protein stimulant, GTP gamma S, led to an enhanced
production of inositol phosphates compared with either alone. Pretreat
ment of the tissue samples with pertussis toxin eliminated all respons
e to sucrose octaacetate plus GTP gamma S, whereas pretreatment with c
holera toxin was without effect. Western blots of solubilized tissue f
rom circumvallate and foliate regions probed with antibodies to the al
pha-subunit of several types of G-proteins revealed bands reactive to
antibodies against G alpha(i1-2), and G alpha(0),, with no apparent ac
tivity to antibodies against G alpha(i3). Given the results from the i
mmunoblots and those of the toxin experiments, it is proposed that the
transduction of the bitter taste of sucrose octaacetate in mice invol
ves a receptor-mediated activation of a G(i)-type protein which activa
tes a phospholipase C to produce the two second messengers, IP3 and DA
G.