Figure 8

Hyperlocomotion induced by MK-801 in 3MST-KO rats. a. Time course of the distance traveled by the wild-type (WT) (nā=ā12), 3MST-KO (nā=ā12), and TRPA1-KO (nā=ā12) rats before and after administration of MK-801(0.2Ā mg/kg). Two-way ANOVA (genotypeāĆātime) showed a significant effect of genotype (F(2, 33)ā=ā16.88, pā<ā0.01) and time (F(17, 561)ā=ā471.42, pā<ā0 .01). The interaction between genotype and time was also significant (F(34, 561)ā=ā7.88, pā<ā0.01). Bonferroniās post-hoc test revealed that 3MST-KO rats had significantly higher locomotor activity compared to wild-type rats from 10Ā min after the MK-801 administration onwards. b. Comparison of the total distance traveled by wild-type, 3MST-KO, and TRPA1-KO rats. ANOVA showed that there were significant differences between the groups in the total distance traveled after the injection of MK-801 (F(2,35)ā=ā20.76, pā<ā0.01) but not before the injection (F(2,35)ā=ā1.13, pā=ā0.33). Bonferroni's posthoc test showed that the total distance traveled was significantly greater in 3MST-KO rats than in the wild-type and TRPA1-KO rats (pā<ā0.01). *pā<ā0.05, **pā<ā0.01, significantly different as indicated. All data shown are meansā±āSEM.