Table 3.
Effects of carcinine on the learning deficit induced by scopolamine (1 mg kg−1) as evaluated by passive avoidance test in mice
Drug | Dose | Training trial | Test trial |
---|---|---|---|
Saline+saline | — | 8.0±4.3 | 288.0±36.0 |
Scopolamine+saline | 1 mg kg−1, i.p. | 8.2±3.5 | 56.6±29.5** |
Scopolamine+thioperamine | 10 mg kg−1, i.p. | 9.2±4.2 | 216.7±62.8# |
Scopolamine+carcinine | 5 mg kg−1, i.p. | 7.8±3.3 | 75.6±27.6 |
10 mg kg−1, i.p. | 6.9±3.0 | 105.8±38.8 | |
20 mg kg−1, i.p. | 7.2±4.4 | 156.6±70.2# | |
Scopolamine+carcinine | 20 mg kg−1, i.p. | ||
+(R)-α-methylhistamine | 1 μg, i.c.v. | 8.0±2.6 | 108.3±47.1 |
2 μg, i.c.v. | 7.7±2.9 | 58.9±24.7& | |
5 μg, i.c.v. | 8.2±3.5 | 32.1±14.2&& | |
Scopolamine+carcinine | 20 mg kg−1, i.p. | ||
+α-fluoromethylhistidine | 10 mg kg−1, i.p. | 10.6±4.5 | 80.6±43.7 |
20 mg kg−1, i.p. | 9.3±3.3 | 50.0±29.8& |
Each value is expressed as the mean±s.d. of 15 to 18 rats.
P<0.01 represents statistically significant difference as compared to the saline+saline control group.
P<0.05 represents statistically significant difference as compared to the scopolamine+saline group.
P<0.05
P<0.01 represent statistically significant difference as compared to the scopolamine+carcinine (20 mg kg−1)-treated group.