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Fig. 7 Effect of Leea macrophylla on mean escape latency in acquisition trial for Wistar albino rats.
Male and female rats completed an acquisition trial followed by an inter-trial interval of a specified length, then a final retention trial.
The injection of saline or tetracaine was applied 5 min before or 5, 90, and 360 min after the acquisition trial and 5 min before the retention tests.
The time that the rats spent in overt exploration of the to-be-remembered objects during the acquisition trial was not affected, suggesting that the drug may have impaired processes of memory formation independently of interference with attention.
Parasagittal cerebellar slices (200 µm thick) were prepared 24 h after the acquisition trial following standard procedures [15], [17].
Each acquisition trial was initiated by placing an individual mouse into the water facing the outer edge of the maze at one of the four designated starting points in quasi-random order.
Similar(12)
Acquisition trials were divided into 10 blocks of 5 trials for a total of 50 trials.
Our results show that increasing the number of acquisition trials results in a change of the internal representation of stimuli.
To this end, we reduced magnitude of conditioning by decreasing US intensity and number of acquisition trials.
In each condition, participants completed 99 or 297 acquisition trials before a delayed retention test similar for all participants.
The results suggest that self-stimulation either before or after avoidance learning improved acquisition performance, but acquisition was maximal when stimulation was also given during acquisition trials.
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