Fig. 3.

Charybdotoxin did not suppress CPA-triggered Ca²⁺ influx in astrocytes. Astrocytes were bathed in Ca²⁺-free solution in the absence or presence of a BKCa channel blocker charybdotoxin (100 nM); they were then exposed to 50 μM CPA followed by replenishment of 2 mM CaCl₂. Quantification of the Ca²⁺ release component (a) and the Ca²⁺ influx component (b). Results are mean ± SEM of 26–56 cells from 3–5 separate experiments