A QUANTITATIVE STUDY OF DUAL-ACTION OF NICKEL IONS ON THE TASTE RESPONSE TO CALCIUM-IONS OF SINGLE FIBERS OF THE FROG GLOSSOPHARYNGEAL NERVE - INHIBITION AND ENHANCEMENT BY NICKEL IONS
Y. Kitada, A QUANTITATIVE STUDY OF DUAL-ACTION OF NICKEL IONS ON THE TASTE RESPONSE TO CALCIUM-IONS OF SINGLE FIBERS OF THE FROG GLOSSOPHARYNGEAL NERVE - INHIBITION AND ENHANCEMENT BY NICKEL IONS, Chemical senses, 19(5), 1994, pp. 401-411
Unitary discharges from single water fibers of the frog glossopharynge
al nerve, caused by stimulation with 0.02-5 mM CaSO4, were recorded fr
om fungiform papillae with a suction electrode. NiSO4 at concentration
s of 0.2-2 mM, namely, at concentrations that are barely effective in
producing impulses, had a dual action on the Ca2+ response: NiSO4 caus
ed both inhibition and enhancement of the Ca2+ response. In the presen
t study, this dual action of Ni2+ ions on the Ca2+ response was invest
igated in detail. Single water fibers yielded a saturation type of con
centration-response curve for CaSO4, which suggested that sulfate ions
do not affect the Ca2+ response. Thus, sulfates were used as test sal
ts in the present study. At low concentrations of Ca2+ ions, Ni2+ ions
inhibited the Ca2+ response, but at higher concentrations of Ca2+ ion
s they enhanced it. The results can be explained quantitatively by the
hypothesis that Ni2+ ions inhibit the Ca2+ response by competing with
Ca2+ ions for the Ca2+ receptor (X(Ca)) that is responsible for the C
a2+ response and that Ni2+ ions enhance the Ca2+ response by acting on
a membrane element that interacts with X(Ca). Double-reciprocal plots
of the data indicate that the enhancing action of Ni2+ ions is satura
ted at 1-2 mM Ni2+ ions and that Ni2+ ions at these concentrations inc
rease the maximal response of the Ca2+ response by 182%. Dissociation
constants for the Ca-X(Ca) complex and the Ni-X(Ca) complex were 4.2 x
10(-5) M and 7.6 x 10(-5) M, respectively. The analysis suggests that
Ni2+ ions enhance the Ca(2+)response by affecting the Ca-X(Ca) comple
x without altering the affinity of X(Ca) for Ca2+ ions.