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. 2020 Aug 24;12:100. doi: 10.1186/s13195-020-00667-6

Fig. 4.

Fig. 4

Extracellular recordings in the medial PFC of cortical slices from AppNL and AppNL-G-F mice at 3–4 (a, b) and 6–8 months of age (c, d). a Basal synaptic transmission is unaffected at 3–4 months as shown by the input-output curves. b Long-term potentiation induced by 4× HFS in the prelimbic and infralimbic region of the PFC from AppNL-G-F mice is of similar magnitude as from the AppNL littermates, but the potentiation of AppNL-G-F decays faster resulting in a temporary difference to AppNL from 30 min post-induction until 120 min (F(1, 7) = 9.052, p = 0.0197, RM-ANOVA). c Input-output curves indicate a severe reduction in basal synaptic transmission in AppNL-G-F mice at 6–8 months of age (two-way RM-ANOVA F(1, 15) = 16.82, p = 0.0009). d Although LTP of a similar initial magnitude could be induced in AppNL-G-F mice (n = 8), the potentiation was not maintained and declined to baseline. In contrast, AppNL mice (n = 8) expressed a robust LTP that remained at about the same level until the end of recordings resulting in a highly significant genotype difference (RM-ANOVA F(1, 16) = 12.04, p = 0.0032). Data are shown as mean ± SEM. Asterisks indicate difference in fEPSPs between AppNL and AppNL-G-F: *p < 0.05, **p < 0.01, ***p < 0.001 (RM-ANOVA). Insets depict representative analogue traces, taken during baseline recording (solid line), after HFS (long-broken line), 90 min after LTP induction (broken line), and at the end of recording (225 min, dotted line). Note that the analogue traces of AppNL-G-F mice at 90 min and 225 min in b are exactly on top of each other