Table 3:
Ro 63–1908 |
CP-101,606 | ||||||||
---|---|---|---|---|---|---|---|---|---|
Raw Proportion of Responses | Raw Proportion of Responses | ||||||||
Factor | DF | F Statistic | P | ηp2 | Factor | DF | F Statistic | P | ηp2 |
Delay | 1.932, 42.496 | 161.156 | <.001 | .880 | Delay | 1.807, 33.945 | 192.045 | < .001 | .901 |
Schedule | 1,22 | 95.619 | <.001 | .813 | Schedule | 1,22 | 115.905 | < .001 | .847 |
Dose | 3,66 | 8.030 | <.001 | .267 | Dose | 3,63 | 0.853 | .470 | .039 |
Delay × Schedule | 1.932, 42.496 | 17.407 | <.001 | .442 | Delay × Schedule | 1.807, 37.945 | 27.776 | < .001 | .569 |
Delay × Dose | 5.831, 128.282 | 1.606 | .153 | .068 | Delay × Dose | 6.103, 128.168 | 1.050 | .403 | .048 |
Schedule × Dose | 3,66 | 7.845 | < .001a | .263 | Schedule × Dose | 3,63 | 0.455 | .470 | .021 |
Delay × Dose × Schedule | 5.831, 128.282 | 1.646 | .142 | .070 | Delay × Dose × Schedule | 6.103, 128.168 | 0.911 | .536 | .042 |
AUC | AUC | ||||||||
Factor | DF | F Statistic | P | Factor | DF | F Statistic | P | ||
Schedule | 1,22 | 98.519 | < .001 | Schedule | 1,22 | 63.645 | < .001 | ||
Dose | 3,66 | 7.244 | < .001 | Dose | 3,66 | 0.987 | .405 | ||
Schedule × Dose | 3,66 | 7.520 | < .00 lb | Schedule × Dose | 3,66 | 0.636 | .594 | ||
Omissions | Omissions | ||||||||
Schedule | DF | χ2 | n | P | Schedule | DF | χ2 | n | P |
Ascending | 3 | 4.263 | 12 | .234 | Ascending | 3 | 2.000 | 12 | .572 |
Descending | 3 | 0.143 | 12 | .986 | Descending | 3 | 3.667 | 12 | .300 |
To probe the significant interaction, separate two-way ANOVAs were conducted for each schedule, with delay and dose as within-subjects factors. For rats tested in the ascending schedule, there was a main effect of delay only, F(1.212, 13.332) = 83.157, p < .001, ηp2 = .883. For rats tested in the descending schedule, there were main effects of delay, F(1.820, 20.019) = 98.174, p < .001, ηp2 = .899, and dose, F(3, 33) = 11.334, p < .001, ηp2 = .507, as well as a significant delay × dose interaction, F(12, 132) = 2.256, p = .012, ηp2 = .170. Ro 63–1908 (1.0 mg/kg) significantly decreased responding at the 30-s, t(11) = 3.261, p = .008, d = −1.040, and 60-s, t(11) = 3.207, p = .008, d = −1.158, delays relative to vehicle.
Contrasts showed that Ro 63−1908 did not affect AUCs in rats trained on the ascending schedule (all p’s ≥.208), whereas Ro 63−1908 (1.0 mg/kg) significantly decreased AUCs (p = .008).