Bursting pacemaker neurons of the snail Helix pomatia were voltage-cla
mped and Ca currents in response to depolarizing steps were recorded.
Simultaneously, changes in intracellular Ca concentrations were measur
ed using the fluorescent dye fura-2 and a highly sensitive digital cam
era. Ca influx through voltage-gated channels induced a spatially non-
uniform increase in intracellular Ca. The Ca signals decayed with a ti
me constant of about 5 s. By increasing the concentration of the indic
ator dye, its Ca-buffering capacity was enhanced and Ca transients in
response to depolarization were diminished. Thereby, the endogenous Ca
buffer capacity could be determined and was calculated to be about 48
0 buffered ions for every free Ca ion. The buffer capacity did not var
y significantly with the amount of Ca influx within the range tested,
suggesting that the buffer is not saturated at Ca concentrations of up
to 1 mu M.