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First, nonspatial visual recognition memory was examined using a hippocampal-dependent NOD task (Hammond et al, 2004; Broadbent et al, 2004) based on rodents innate preference for novelty, rather than food reward or negative reinforcement, which therefore involves similar motivational conditions to those under which human memory is normally assessed.
At a time when all subjects were adults, spatial working memory was examined in the absence and presence of an acute ethanol challenge.
Visual recognition memory was examined by using a novel object recognition test as described previously [64].
Long-term memory was examined at 1 day and 10 days after the training with two separate sets of mice.
Spatial learning and memory was examined with a Morris water-maze as described in our previous publication [38].
Likewise, the treatment effect in spatial memory was examined also by a two-way repeated measures ANOVA test (treatment × trial) followed by post hoc Scheffe's analysis.
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Main effects of mood, stimulus valence and memory were examined as was activity related to successful memory formation during congruent and in-congruent moods.
Learning and memory were examined in a spatial holeboard task and brains were analyzed using quantitative histochemical, morphological and biochemical techniques.
Antagonists of alpha 7 and alpha 4 beta 2 receptors were locally infused into the ventral hippocampus of rats and the effects on memory were examined with the radial-arm maze.
Gender, FSIQ, auditory working memory, and visual-spatial working memory were examined as covariates.
Both recognition memory and recency memory were examined in rats with cytotoxic lesions of the anterior thalamic nuclei.
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