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. 2023 Apr 5;14:1880. doi: 10.1038/s41467-023-37601-x

Fig. 6. A2AR are selectively upregulated in the lateral septum (LS) of mice subject to chronic restraint stress (CRS).

Fig. 6

ad Compared with control mice, CRS mice showed an increase in immobility time in a tail suspension test (TST) (n = 11 and 13 mice per group for no-stress and CRS, respectively, Unpaired t test, p = 0.00001, t(22) = 5.674) (a), without changes in the total distance traveled in an open field test (OFT) (n = 11 and 13 mice per group for no-stress and CRS, respectively, Unpaired t test, p = 0.8169, t(22)=0.2343) (b). CRS mice spent similar time in the center area of the OFT (n = 11 and 13 mice per group for no-stress and CRS, respectively, Mann-Whitney test, p = 0.0821, U = 41) (c) and in the open arms of an elevated O-maze test (n = 11 and 13 mice per group for no-stress and CRS, respectively, Unpaired t test, p = 0.1165, t(22) = 1.634) (d). e, f Representative Western blot and quantification of A2AR protein levels in the septum (n = 6 mice/group, Unpaired t test, p = 0.0050, t(10) = 3.584), striatum (n = 6 mice/group, Unpaired t test, p = 0.9898, t(10) = 0.01314), prefrontal cortex (PFC) (n = 6 mice/group, Unpaired t test, p = 0.08, t(10) = 1.948) and hippocampus (n = 6 mice/group, Unpaired t test, p = 0.0886, t(10) = 1.886) of CRS and control mice. CRS mice displayed a selective upregulation of A2AR in the septum without significant changes in the other three brain regions associated with mood processing. Data were shown as mean ± SEM. **p < 0.01, ***p < 0.001; n.s., no significant difference. Source data are provided as a Source Data file.