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. Author manuscript; available in PMC: 2013 Apr 1.
Published in final edited form as: Psychopharmacology (Berl). 2011 Oct 1;220(4):673–685. doi: 10.1007/s00213-011-2516-9

Table 3.

Pretreatment-induced shifts in cocaine dose-effect function

Pretreatment - genotype A50 cocaine alone A50 pretreatment Fold shift Rate decrease
Xanomeline - Wild-type 1.58 [0.96 – 2.61] 8.87 [4.05 – 19.4]* 8.1 −36% [−10 – −62]
Xanomeline - M1−/− 1.81 [1.64 – 2.00] 5.18 [3.50 – 7.65]* 3.1 −36% [−19 – −54]
Xanomeline - M4−/− 0.99 [0.49 – 1.99] 5.22 [1.86 – 20.3] 8.6 ns
VU0357017 - Wild-type 1.25 [0.74 – 2.10] 4.95 [2.81 –8.73]* 5.5 ns
VU0357017 - M1−/− 1.43 [1.07 – 1.90] 1.24 [0.67 – 2.28] 1.0 ns
VU0357017 - M4−/− 2.04 [0.85 – 4.93] 3.49 [1.84 – 6.62] 2.1 ns
77-LH-28-1 - SW 0.80 [0.51 – 1.27] 2.32 [1.03 – 5.21] 4.1 −18% [−4 – −31]
*

non-overlapping 95% confidence intervals. Fold shift in A50 was calculated in each mouse, then averaged. Rate decrease was calculated as the % decrease from cocaine alone in each mouse, then averaged across mice and cocaine doses.

ns: non-significant.

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