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. Author manuscript; available in PMC: 2011 May 24.
Published in final edited form as: Endocrinology. 2005 Jun 2;146(9):4090–4096. doi: 10.1210/en.2004-1285

Fig. 3.

Fig. 3

Early-life treatment with CRF1 antagonist improves memory in the relatively stress-free, object recognition test. Data are given as the mean number of seconds (±se) spent exploring each object on d 1 (A) and on d 2 (B), the test day. A, Day 1: upper panel, naive (solid blue bars; n = 9) and vehicle-treated (empty blue bars; n = 6) nonhandled groups; middle panel, naive (solid magenta bars; n = 8) and vehicle-treated (empty magenta bars; n = 3) handled groups. These panels show that object exploration times did not differ between naive and vehicle-treated subgroups. Lower panel, Therefore, the naive and vehicle subgroups were consolidated to compare time spent exploring object 1 (labeled as 1′ for each group) and object 2 (labeled as 2′ for each group). NH, Nonhandled rats; H, handled; NH+A, CRF1 antagonist-treated nonhandled rats (n = 10); H+A, antagonist-treated handled rats (n = 8). Note that on the first day, all groups explored each object for similar amounts of time. B, Day 2, The ratio of time spent exploring the novel object/time spent exploring the familiar object on d 2. A score of 1 indicates that both objects were explored for similar amounts of time. Administration of CRF1 antagonist did not modify the ratio of time spent exploring novel vs. familiar objects in handled rats. However, it significantly increased this ratio in the nonhandled rats. *, P < 0.05, significantly different from the nonhandled group. The values of H, H+A, and NH+A groups are not significantly different.

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