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. 2006 Jan 19;571(Pt 3):605–618. doi: 10.1113/jphysiol.2005.103812

Figure 5. Acute and chronic CTZ modulation of mEPSCs in hippocampal cultures.

Figure 5

A–C, typical mEPSC traces recorded in the presence of TTX (0.5 μm) and BIC (20 μm) in control (A), acute application (B), and after chronic pretreatment (C) with CTZ (both 5 μm). Insets at the bottom of each panel are the averaged mEPSCs, showing a slowed decay phase after acute application of CTZ (B) but not chronic CTZ-pretreatment (C, after washout of CTZ). D, bar graphs showing that the normalized mEPSC frequency was significantly increased to 147 ± 11% during acute CTZ application (P < 0.02), and to 193 ± 35% after chronic CTZ pretreatment (P < 0.05). E, bar graphs showing that the normalized mEPSC amplitude was not significantly changed during acute application (107 ± 6%, P > 0.3) or after chronic pretreatment with CTZ (119 ± 12%, P > 0.05). F, kinetics analysis showing a significant increase in the normalized decay time constant during acute application of 5 μm CTZ (156 ± 12%, P < 0.003), but not after chronic pretreatment with CTZ (91 ± 10%, P > 0.5).

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