Voltage-evoked [Ca2+]i
rise is sensitive to extracellular Ca2+ channel blockers.
A, [Ca2+]i increases (trace below) and clamp
current (trace above) during 20-s steps from −50 to −200 mV (⊔,
above) before and after adding 0.1 mm GdCl3 to
the bath. Period of GdCl3 exposure is indicated by the open
bar. Data are from one guard cell in 5 mm
Ca2+-Mes, pH 6.1, with 10 mm KCl. Inset, Clamp
current during steps to −200 mV (⊔, above) replotted on expanded
time scale shows characteristic activation of the
IK,in current (Grabov and Blatt, 1997) when
the [Ca2+]i rise is suppressed in the
presence of Gd3+ (fine line) and its time-dependent
inactivation when [Ca2+]i rises in the
absence of Gd3+ (solid line). B,
[Ca2+]i increases evoked during 20-s steps
from −50 to −200 mV (⊔, above) before and after adding 0.5
μm calcicludine to the bath. Data are from one guard cell
in 5 mm Ca2+-Mes, pH 6.1, with 10
mm KCl. Period of exposure to the Ca2+ channel
blocker is indicated by an open bar. Time scale (below), 2
min.