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. Author manuscript; available in PMC: 2021 Jun 9.
Published in final edited form as: Nature. 2020 Dec 9;589(7842):474–479. doi: 10.1038/s41586-020-3008-z

Extended Data Fig. 6. High doses of TBG do not produce a conditioned place preference (CPP).

Extended Data Fig. 6.

(a) Schematic illustrating the design of the CPP experiments. On day 1, the amount of time the mice spent in each distinct side of a two-chamber apparatus was recorded. Next, VEH and TBG were administered to mice on alternating days while they were confined to chamber A (white box) or B (gray parallel lines), respectively. Conditioning lasted for a total of 6 days. On day 8, preference for each distinct side of the two-chamber apparatus was assessed. (b) A low dose of TBG (1 mg/kg) did not produce CPP or conditioned place aversion (CPA). Higher doses (10 and 50 mg/kg) produce a modest CPA. (c) TBG does not produce any long-lasting (>24 h) effects on locomotion. There is no statistical difference in locomotion between any pre- or post-conditioning groups (p = 0.9985, one-way ANOVA). White bars indicate groups prior to receiving TBG (i.e, pre-conditioning), while blue bars indicate groups 24 h after the last TBG administration (i.e, post-conditioning). Exact N numbers for each experimental condition are reported in Supplementary Table 1. Specific statistical tests, information on reproducibility, and exact p values are reported in the Methods and Supplementary Table 1.