Skip to main content
. 2020 Dec 2;62:103130. doi: 10.1016/j.ebiom.2020.103130

Fig. 6.

Fig. 6

Effect of the PPARα agonist fenofibrate.

(a) Schedule of treatment with fenofibrate.

(b) Morphological classification of spines in saline-administered mice (4 mice, 8 cells) and phencyclidine (PCP)-administered mice (3 mice, 8 cells). The values represent the mean ± standard error. The data were analyzed using unpaired t-tests.

(c) Morphological classification of spines in saline/vehicle-administered mice (4 mice, 10 cells), saline/fenofibrate-administered mice (6 mice, 10 cells), PCP/vehicle-administered mice (4 mice, 10 cells), and PCP/fenofibrate-administered mice (5 mice, 10 cells). The values represent the mean ± standard error. The data were analyzed using one-way ANOVA (p < 0.001), followed by Tukey's test.

(d) Experimental design for the MK-801-induced locomotor hyperactivity test following chronic administration of fenofibrate.

(e) Locomotor activity before and after a single injection of MK-801 (0.15 mg/kg body weight). The values represent the mean ± standard error. The data were analyzed using two-way repeated-measures ANOVA (drug effect, p < 0.001).

(f) Cumulative locomotor activity before and after MK-801 injection. The values represent the mean ± standard error. The data were analyzed using unpaired t-tests.