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. 2010 Dec 8;30(49):16585–16600. doi: 10.1523/JNEUROSCI.3958-10.2010

Table 1.

Statistical results for all figures

Figure(s) Dependent variable Factor(s) Results
1C Rewards earned Drug dose 0 s ITI: F(6,7) = 2.4, p = 0.04, n = 8 rats
3 s ITI: F(6,6) = 4.2, p = 0.003, n = 7
10 s ITI: F(6,7) = 5.5, p < 0.001, n = 8
20 s ITI: F(6,6) = 11.5, p < 0.001, n = 7
1D,E, S2A Log latency between events (cue-lever press, lever press-entry, consummatory) Interval, drug dose Interaction interval × drug dose:
0 s ITI: F(12,7) = 0.8, p = 0.7
3 s ITI: F(12,6) = 2.5, p = 0.008
10 s ITI: F(12,6) = 2.6, p = 0.006
20 s ITI: F(12,6) = 11.3, p < 0.001
1F Rewards earned Drug dose 0 s ITI core: F(6,7) = 1.6, p = 0.18, n = 8
0 s ITI shell: F(6,7) = 1.5, p = 0.2, n = 8
20 s ITI core: F(6,7) = 6.8, p < 0.001, n = 8
20 s ITI shell: F(6,7) = 5.7, p < 0.001, n = 8
1G,H, S2B Log latency between events (cue-lever press, lever press-entry, consummatory) Interval, drug dose Interaction interval × drug dose:
0 s ITI core: F(12,7) = 1.0, p = 0.5
0 s ITI shell: F(12,6) = 1.6, p = 0.1
20 s ITI core: F(12,4) = 3.3, p = 0.001
20 s ITI shell: F(12,7) = 4.9, p < 0.001
2A, inset Log latency between receptacle exit and lever press ITI Non-repeated-measures ANOVA:
F(3,58) = 320, p < 0.001
2B, inset Log latency between lever press and receptacle entry ITI Non-repeated-measures ANOVA:
F(3,58) = 6.4, p < 0.001
2C % of trials Drug dose Near lever: F(2,5) = 7.8, p = 0.016, n = 6 rats
Far from lever:: F(2,5) = 11.8, p = 0.006
2D Log latency between cue onset and lever press Location, drug dose Location: F(1,4) = 47.9, p = 0.002
Drug dose: F(2,4) = 5.0, p = 0.04
Interaction location × drug dose: F(2,4) = 0.3, p = 0.7
3A % of trials Drug dose Task activity: F(2,5) = 9.3, p = 0.011, n = 6 rats
Immobility: F(2,5) = 13.8, p = 0.004
Locomotion: F(2,5) = 0.9, p = 0.45
Grooming: F(2,5) = 1.5, p = 0.29
3B Log latency between cue onset and lever press Action at cue onset, drug dose Action at cue onset: F(3,4) =71.6, p < 0.001
Drug dose: F(2,4) = 6.1, p = 0.02
Interaction action × drug dose: F(6,4) = 0.4, p = 0.9
3B, inset Log latency between cue onset and lever press Drug dose Lever pressing: F(2,5) = 10.4, p = 0.006
3C % of trials press Drug dose Immediate response: F(2,5) = 14.0, p = 0.004
Immobility: F(2,5) = 8.1, p = 0.015
Locomotion: F(2,5) = 6.0, p = 0.03
Grooming: F(2,5) = 1.5, p = 0.28
3D Log latency between cue onset and lever press Action after cue onset (comparison with Immediate Response), drug dose Immobility vs immediate response:
Action: F(1,4) = 208.6, p < 0.001
Drug dose: F(2,4) = 11.5, p = 0.003
Interaction action × drug dose: F(2,4) = 2.2, p = 0.2
Locomotion vs immediate response:
Action: F(1,4) = 201.1, p < 0.001
Drug dose: F(2,4) = 16.5, p < 0.001
Interaction action × drug dose: F(2,4) = 3.4, p = 0.1
Grooming vs immediate response:
Action: F(1,3) = 77.9, p = 0.003
Drug dose: F(2,3) = 11.3, p = 0.009
Interaction action × drug dose: F(2,3) = 3.7, p = 0.09
4C Cue response ratio Location, drug dose DS:
Location: F(2,4) = 16.8, p = 0.001
Drug dose: F(6,4) = 9.5, p < 0.001
Interaction location × drug dose: F(12,4) = 1.0, p = 0.4
NS: all main & interaction F > 0.2
n = 6 rats
4D Movement velocity Movement type, drug dose Movement type: F(3,4) = 12.2, p < 0.001
Drug dose: F(6,4) = 1.6, p = 0.2
Interaction movement type × drug dose:
F(18,4) = 1.4, p = 0.2
(post hoc tests show post-DS movements resulting in lever press to be faster than each other type of movement, irrespective of drug dose)
4E First movement log latency Cue, drug dose Interaction cue × drug dose:
F(6,4) = 4.2, p = 0.005
5C Rewards earned Drug dose Cue 1: F(6,6) = 0.7, p = 0.7, n = 7 rats
Cue 2: F(6,6) = 0.7, p = 0.7
5D Log latency to reach receptacles 1 and 2 Drug dose Cue 1–receptacle 1 entry latency: F(6,6) = 2.3, p = 0.06
Cue 2–receptacle 2 entry latency: F(6,6) = 7.1, p < 0.001
5E % of trials Drug dose F(6,6) = 0.2, p = 0.97
5F % of trials Drug dose F(6,6) = 1.5, p = 0.2
5G Log latency to respond to cue 3 Drug dose Cue 3–receptacle 2 exit latency: F(6,6) = 1.0, p = 0.5
Receptacle 2 exit–receptacle 1 entry latency: F(6,6) = 1.6, p = 0.2
7C Log latency between events Interval, drug Interaction interval × drug:
F(2,7) = 5.7, p = 0.02, n = 9 rats
7E, inset % of trials Drug F(2,8) = 0.7, p = 0.5
7F Log latency between lever presses Distance traveled, drug dose Interaction distance traveled × drug:
F(2,7) = 4.4, p = 0.03
7G Velocity of last movement before lever press Interval, drug Interval: F(1,7) = 6.5, p = 0.04
Drug: F(1,7) = 3.5, p = 0.06
Interaction interval × drug:
F(2,7) = 0.3, p = 0.7

Unless otherwise noted, all tests are repeated-measures ANOVA with one or two factors.