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Medial prefrontal lesions impair performance in an operant delayed nonmatch to sample working memory task
Laura J Benoit1, Emma S Holt2, Eric Teboul2
1Department of Neurobiology and Behavior, Graduate School of Arts and Sciences, Columbia University.
Behavioral Neuroscience
|March 6, 2020
Summary
Working memory relies on the medial prefrontal cortex (mPFC). A new operant task confirmed mPFC
Area of Science:
- Neuroscience
- Cognitive Science
- Behavioral Science
Background:
- Working memory is crucial for cognitive function and is often impaired in psychiatric disorders.
- The medial prefrontal cortex (mPFC) is implicated in working memory processes.
- Traditional maze tasks for studying mPFC in working memory are time-consuming and have high exploratory components.
Purpose of the Study:
- To investigate the role of the mPFC in working memory using a novel operant-based delayed nonmatch to sample (DNMS) task.
- To assess the mPFC's involvement in both the acquisition and performance phases of a working memory task with varying delays.
Main Methods:
- Excitotoxic lesions were created in the mPFC of mice.
- Mice were trained and tested on an operant DNMS working memory task.
- Performance was evaluated based on task acquisition and accuracy with introduced delays.
Main Results:
- Mice with mPFC lesions showed significant impairments in acquiring the DNMS task without delay.
- Lesioned mice also exhibited deficits in performing the task when delays were introduced.
- No differences were observed in trial length, reward collection, or lever-press latencies, ruling out motivation or mobility changes.
Conclusions:
- The operant DNMS task is dependent on the mPFC for working memory function.
- This task provides a more efficient method for studying mPFC-dependent working memory.
- The findings facilitate research into the physiology and circuit mechanisms of working memory.
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