Table 3. The effects of exposure to chronic, unpredictable stress (CUS) and/or concurrent treatment with the antidepressant imipramine (IMI; 10 mg/kg) on the tissue content (nmol/g tissue) of the endocannabinoid 2-arachidonylglycerol (2-AG).
Exposure of male rats to 21 days of CUS resulted in a significant increase in 2-AG content within the hypothalamus and the midbrain, neither of which was reversed by concurrent IMI treatment. Significant differences from non-stressed (CON), vehicle (VEH) treated animals (p < 0.05) denoted by *. For all treatment conditions, n = 7–8. Data are presented as mean nmol/g tissue +/− SEM.
| CON/VEH | CUS/IMI | CON/VEH | CUS/IMI | |
|---|---|---|---|---|
| Prefrontal Cortex | 4.35 +/− 0.29 | 5.16 +/− 0.14 | 5.60 +/− 0.45 | 5.63 +/− 0.52 |
| CUS × IMI F (1, 27) = 0.82, p > 0.05; CUS F (1, 27) = 0.93, p > 0.05; IMI F (1, 27) = 3.93, p > 0.05 | ||||
| Hippocampus | 6.37 +/− 0.64 | 6.11 +/− 0.45 | 6.82 +/− 0.69 | 7.04 +/− 0.59 |
| CUS × IMI F (1, 26) = 0.08, p > 0.05; CUS F (1, 26) = 0.00, p > 0.05; IMI F (1, 26) = 1.28, p > 0.05 | ||||
| Hypothalamus | 8.25 +/− 0.96 | 12.92 +/− 0.60* | 8.38 +/− 0.76 | 13.56 +/− 0.98* |
| CUS × IMI F (1, 25) = 0.10, p > 0.05; CUS F (1, 25) = 35.76, p < 0.001; IMI F (1, 25) = 0.22, p > 0.05 | ||||
| Ventral Striatum | 5.81 +/− 0.77 | 6.26 +/− 0.45 | 4.71 +/− 0.27 | 5.68 +/− 0.26 |
| CUS × IMI F (1, 27) = 0.32, p > 0.05; CUS F (1, 27) = 2.41, p > 0.05; IMI F (1, 27) = 3.33, p > 0.05 | ||||
| Amygdala | 9.57 +/− 0.68 | 8.84 +/− 1.04 | 7.91 +/− 0.94 | 10.60 +/− 1.08 |
| CUS × IMI F (1, 25) = 3.00, p > 0.05; CUS F (1, 25) = 0.98, p > 0.05; IMI F (1, 25) = 0.00, p >0.05 | ||||
| Midbrain | 4.00 +/− 0.31 | 5.71 +/− 0.44* | 5.02 +/− 0.40 | 5.73 +/− 0.19* |
| CUS × IMI F (1, 27) = 2.03, p > 0.05; CUS F (1, 27) = 11.89, p < 0.005; IMI F (1, 27) = 2.20, p > 0.05 | ||||