FIGURE 5.

De novo translation and transcription are required for LTM, but not for STM. Animals were cultured on agar plates containing anisomycin, cycloheximide, or actinomycin D for 4 h (massed training) or 2 h (spaced training) at RT, and were then conditioned with 0.01% 1-nonanol and 160 mM KCl by eight-cycle massed training (open bars) or eight-cycle spaced training with a 10-min ITI (gray bars). Chemotaxis assays were performed immediately after training. LI values were calculated from the equation shown in Figure 2A using CIreference values of unpaired animals treated with 0.01% 1-nonanol and 160 mM KCl (ISI, 120 s). Asterisks (∗∗) indicate statistically significant differences (p < 0.01) determined by one-way ANOVA, followed by the Tukey-Kramer test for further comparison with LIs of untreated animals. Bars are means ± SEM (n = 6–9 assays).