Open AccessMedial prefrontal lesions impair performance in an operant delayed nonmatch to sample working memory task.
Author(s) -
Laura Benoit,
Emma S Holt,
Eric Teboul,
Joshua P Taliaferro,
Christoph Kellendonk,
Sarah Canetta
Publication year - 2020
Publication title -
behavioral neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 140
eISSN - 1939-0084
pISSN - 0735-7044
DOI - 10.1037/bne0000357
Subject(s) - working memory , psychology , prefrontal cortex , neuroscience , task (project management) , cognition , short term memory , interference theory , cognitive psychology , management , economics
Cognitive functions, such as working memory, are disrupted in most psychiatric disorders. Many of these processes are believed to depend on the medial prefrontal cortex (mPFC). Traditionally, maze-based behavioral tasks, which have a strong exploratory component, have been used to study the role of the mPFC in working memory in mice. In maze tasks, mice navigate through the environment and require a significant amount of time to complete each trial, thereby limiting the number of trials that can be run per day. Here, we show that an operant-based delayed nonmatch to sample (DNMS) working memory task, with shorter trial lengths and a smaller exploratory component, is also mPFC-dependent. We created excitotoxic lesions in the mPFC of mice and found impairments in both the acquisition of the task, with no delay, and in the performance with delays introduced. Importantly, we saw no differences in trial length, reward collection, or lever-press latencies, indicating that the difference in performance was not due to a change in motivation or mobility. Using this operant DNMS task will facilitate the analysis of working memory and improve our understanding of the physiology and circuit mechanisms underlying this cognitive process. (PsycInfo Database Record (c) 2020 APA, all rights reserved).