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. 1999 Jan;119(1):277–288. doi: 10.1104/pp.119.1.277

Figure 5.

Figure 5

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.