Evidence of action sequence chunking in goal-directed instrumental conditioning and its dependence on the dorsomedial prefrontal cortex.
Open accessAbstract
The current study investigated the contribution of the dorsomedial prefrontal cortex (dmPFC) to instrumental action selection. We found that cell body lesions of the dmPFC, centered on the medial agranular area, spared rats' ability to choose between actions based on either the value or the discriminative stimulus properties of an outcome. We next examined the effects of these lesions on action sequence learning using a concurrent bidirectional heterogeneous chain task in which the identity of the reward delivered was determined by the order in which the two lever press actions were performed. Although both lesioned rats and sham controls learned to perform the task, we found that they relied on different behavioral strategies to do so. In subsequent tests, rats in the sham group were able to withhold their performance of a sequence when either its associated outcome was devalued or the contingency between that sequence and its outcome was degraded by delivering the outcome noncontingently. Interestingly, lesioned rats failed to reorganize their performance at the action sequence level and, rather, were found to withhold their performance of the terminal response in the sequence that had earned the devalued outcome relative to the more distal response, suggesting that they represented the elements of the sequence as distinct behavioral units. These findings demonstrate that rats can use sequence-level representations, or action chunks, to organize their behavior in a goal-directed manner and indicate that the dmPFC plays a critical role in this process.
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The increase in dopaminergic and noradrenergic availability in the PFC of SHR rats might be critical in restoring goal-directed actions by enhancing attentional mechanisms necessary for carrying out goal-directed behavior.
“Thus, the increase in dopaminergic and noradrenergic availability in the PFC of SHR rats might be critical in restoring goal-directed actions by enhancing attentional mechanisms necessary for carrying out goal-directed behavior (Ostlund and Balleine, 2005; Ostlund et al., 2009).”
From The Effects of Methylphenidate on Goal-directed Behavior in a Rat Model of ADHD (2015) · cites this paper as Ostlund et al., 2009
The Discussion reports that the dorsomedial PFC helps rats use action-sequence representations in a goal-directed manner. It does not address SHR rats, increased dopamine or noradrenaline availability, or an attentional mechanism for restoring goal-directed actions. The paper also limits the dmPFC’s role to action chunking rather than goal-directed action selection generally. (LLM, conf=0.82)
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Cites
Habits, Rituals, and the Evaluative Brain
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Motivational control of goal-directed action
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Self-citationRay, J. P., & Price, J. L. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903230204 · Cited by 326 · see citing works
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Habits, action sequences and reinforcement learning
Dezfouli, A., & Balleine, B. W. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08050.x · Cited by 297 · see citing works
Self-citationInterplay of approximate planning strategies
Huys, Q. J. M., Lally, N., Faulkner, P., Eshel, N., Seifritz, E., Gershman, S. J., Dayan, P., & Roiser, J. P. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414219112 · Cited by 207 · see citing works
Sex differences in effective fronto-limbic connectivity during negative emotion processing
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Premotor cortex is critical for goal-directed actions
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The Effects of Methylphenidate on Goal-directed Behavior in a Rat Model of ADHD
Natsheh, J. Y., & Shiflett, M. W. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00326 · Cited by 21 · see citing works
- Authors
- Ostlund, S. B., Winterbauer, N. E., & Balleine, B. W.
- Affiliations
- University of California, Los Angeles (US)
- University of Vermont (US)
- The University of Sydney (AU)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2009-06-24
- Volume
- 29
- Issue
- 25
- Pages
- 8280-8287
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6666053
- OpenAlex
- W1981439408
- Cited by
- 103
- References
- 3
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 5 · 2023: 3 · 2022: 4 · 2021: 4 · 2020: 9 · 2019: 8 · 2018: 9 · 2017: 6 · 2016: 11 · 2015: 8 · 2014: 7 · 2013: 2 · 2012: 5
- FWCI
- 2.57
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (T32MH017140, MH 17140)
- National Institute of Child Health and Human Development (#HD59257)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD059257, HD59257)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- dorsomedial prefrontal cortex, operant conditioning, action selection, sequence learning, outcome devaluation, contingency degradation, behavioral strategies, goal-directed behavior, rats
- MeSH terms
- Animals, Association Learning, Behavior, Animal, Brain Injuries, Choice Behavior, Conditioning, Classical, Discrimination Learning, Female, Microinjections, Reaction Time, N-Methylaspartate, Prefrontal Cortex, Excitatory Amino Acid Agonists, Rats, Long-Evans, Rats
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