Failure of rats to acquire a taste reversal learning set

1987 ◽  
Vol 12 (2) ◽  
pp. 333-339 ◽  
Author(s):  
Burton M. Slotnick ◽  
Gary M. Brosvic
2008 ◽  
Vol 58 (1) ◽  
pp. 15-36 ◽  
Author(s):  
Karen M. Lionello-DeNolf ◽  
William J. McIlvane ◽  
Daniela S. Canovas ◽  
Deisy G. de Souza ◽  
Romariz S. Barros

1965 ◽  
Vol 20 (1) ◽  
pp. 271-276 ◽  
Author(s):  
James E. King

Four rock squirrels received 80 discrimination learning-set (DLS) problems followed by 80 reversal learning-set (RLS) problems in a modified WGTA. Each DLS problem was learned to a criterion of 9 out of 10 correct while each RLS problem consisted of either 4, 8, 12, or 16 pre-reversal trials and 12 post-reversal trials. Significant interproblem learning occurred during the DLS problems. DLS learning suggested that, for squirrels, a criterial DLS procedure is more efficient than presentation of a small fixed number of trials per problem. RLS performance became independent of the number of pre-reversal trials during the last block of 16 problems.


1987 ◽  
Vol 510 (1 Olfaction and) ◽  
pp. 627-629 ◽  
Author(s):  
B. M. SLOTNICK ◽  
G. M. BROSVIC ◽  
S. R. PARKER

1966 ◽  
Vol 18 (3) ◽  
pp. 250-253 ◽  
Author(s):  
S. D. Dalrymple ◽  
R. Stretch

Nineteen rats were required to learn a series of 15 position-reversal problems in a T-maze (Phase A) and were then assigned at random to two groups. The acquired position-reversal set (PRLS) was then subjected to disruption over 80 trials in which different reward treatments operated for each group (Phase B). For a further 150 trials following the disruptive phase, the initial conditions were reinstated (Phase C). Results showed that rats receiving non-reinforcement during Phase B returned to the asymptotic performance recorded in Phase A within 2-3 reversal problems while those receiving 20 per cent, random reinforcement during Phase B failed to re-acquire the PRLS within 15 reversal problems. The results indicate that random 20 per cent, reinforcement, applied after establishment of a PRLS in rats, displaces by persistent random-responding, the “Win-stay-Lose-shift” hypothesis appropriate for PRLS attainment.


2021 ◽  
Vol 15 ◽  
Author(s):  
Alican Caglayan ◽  
Katharina Stumpenhorst ◽  
York Winter

Rodent behavioral tasks are crucial to understanding the nature and underlying biology of cognition and cognitive deficits observed in psychiatric and neurological pathologies. Olfaction, as the primary sensory modality in rodents, is widely used to investigate cognition in rodents. In recent years, automation of olfactory tasks has made it possible to conduct olfactory experiments in a time- and labor-efficient manner while also minimizing experimenter-induced variability. In this study, we bring automation to the next level in two ways: First, by incorporating a radio frequency identification-based sorter that automatically isolates individuals for the experimental session. Thus, we can not only test animals during defined experimental sessions throughout the day but also prevent cagemate interference during task performance. Second, by implementing software that advances individuals to the next test stage as soon as performance criteria are reached. Thus, we can prevent overtraining, a known confounder especially in cognitive flexibility tasks. With this system in hand, we trained mice on a series of four odor pair discrimination tasks as well as their respective reversals. Due to performance-based advancement, mice normally advanced to the next stage in less than a day. Over the series of subsequent odor pair discriminations, the number of errors to criterion decreased significantly, thus indicating the formation of a learning set. As expected, errors to criterion were higher during reversals. Our results confirm that the system allows investigating higher-order cognitive functions such as learning set formation (which is understudied in mice) and reversal learning (which is a measure of cognitive flexibility and impaired in many clinical populations). Therefore, our system will facilitate investigations into the nature of cognition and cognitive deficits in pathological conditions by providing a high-throughput and labor-efficient experimental approach without the risks of overtraining or cagemate interference.


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