2.6.1. Open field test

CV Chitra Vinnakota
AS Anna Schroeder
XD Xin Du
KI Kazutaka Ikeda
SI Soichiro Ide
MM Masayoshi Mishina
MH Matthew Hudson
NJ Nigel Charles Jones
SS Suresh Sundram
RH Rachel Anne Hill
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Data from the above locomotor test were used to analyze anxiety‐like behavior as part of the OFT. The arena was divided into a center area (25% of arena) and four equal squared corners (combined, 25% of arena) (Figure 2a). The time spent in the center was calculated using the software PAS764 provided by SD Instruments. Less time spent in the center was taken to represent anxiety/fear‐related behavior.

The effect of NMDAR antagonists on locomotion in WT and GluN2D‐KO mice. (a) Schematic overview of the paradigm. Locomotor activity without drug during the first 1 h (b), and locomotor activity over 2 h following drug challenge (c–g). Average distance traveled (c) and distance traveled over time with either saline (d; n = 9 F WT, 9 F KO, 9 M WT, 10 M KO), R‐norket (e; n = 10 F WT, 10 F KO, 10 M WT, 9 M KO), S‐ket (f; 9 F WT, 9 F KO, 10 M WT, 10 M KO), or PCP (g; 9 F WT, 10 F KO, 10 M WT, 11 M KO). Further measures of ataxia (h), stereotypy (i), and catalepsy (j) were assessed in a separate cohort (n = 10 F WT, 8 F KO, 12 M WT, 12 M KO). All data presented as mean ± SEM. When a two‐way ANOVA showed a significant interaction, p‐values were calculated with the Sidak's multiple comparison test (b, c), Fisher's LSD test (d–f, g: females), Tukey's multiple comparison test (g: males, h–j); *p < .05, **p < .01, ***p < .001, ****p < .0001.

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