Table 3.
Effect of chronic treatment with studied compounds on locomotor activity in mice
Treatment | Dose of the studied compound (mg/kg) | Number of crossings ± S.E.M |
---|---|---|
Saline + vehicle | – | 366.0 ± 59.3 |
Saline + corticosterone | – | 343.4 ± 27.3 |
HBK-14 + corticosterone | 1.25 | 406.3 ± 64.2 |
HBK-14 + corticosterone | 2.5 | 400.8 ± 55.8 |
Fluoxetine + corticosterone | 10 | 423.3 ± 47.3 |
Saline + vehicle | – | 436.9 ± 71.7 |
Saline + corticosterone | – | 394.5 ± 67.1 |
HBK-15 + corticosterone | 0.625 | 466.1 ± 84.8 |
HBK-15 + corticosterone | 1.25 | 478.9 ± 78.8 |
Fluoxetine + corticosterone | 10 | 510.3 ± 54.0 |
Corticosterone (20 mg/kg) was injected subcutaneously (s.c.) for 3 weeks at random times during the light phase. Additionally, 30 min before, corticosterone administration mice were intraperitoneally (i.p.) injected with HBK-14 (1.25 or 2.5 mg/kg), HBK-15 (0.625 or 1.25 mg/kg), fluoxetine (10 mg/kg), or 0.9% NaCl (saline). Control groups received saline (i.p.) and 30 min later saline containing 0.1% dimethyl sulfoxide (DMSO) and 0.1% Tween-80 (vehicle, s.c.). Statistical analysis: one-way ANOVA (Newman–Keuls post hoc); n = 8 mice per group