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. Author manuscript; available in PMC: 2013 Jan 1.
Published in final edited form as: Neurotoxicol Teratol. 2011 Nov 6;34(1):63–71. doi: 10.1016/j.ntt.2011.10.006

Fig. 1.

Fig. 1

Latency in seconds to cross to the dark chamber during each of the 5 acquisition trials (A) and during the three retention tests (B). PND 22 rats received either prenatal vehicle or daily THC exposure. In A, * indicates a significant difference from trial 1 latency assessed with paired t-tests, all with p<0.001. In B * indicates a significant difference from latency at one week (t[45]=5.265, p<0.001). There were no differences in latency across the retention tests for the THC-exposed rats.