Goal-directed actions transiently depend on dorsal hippocampus
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Abstract
The role of the hippocampus in goal-directed action is currently unclear; studies investigating this issue have produced contradictory results. Here we reconcile these contradictions by demonstrating that, in rats, goal-directed action relies on the dorsal hippocampus, but only transiently, immediately after initial acquisition. Furthermore, we found that goal-directed action also depends transiently on physical context, suggesting a psychological basis for the hippocampal regulation of goal-directed action control.
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Information of action-outcome association for goal-directed decision-making, transiently encoded in hippocampus at earlier stages of training, is transferred to RSC-projecting ACC neurons.
“Since both the ACC and RSC are crucial for learning and memory of associative information, which is transferred from the hippocampus28,38, it is conceivable that information of action-outcome association for goal-directed decision-making, which is transiently encoded in the hippocampus at earlier stages of training39, is transferred to the RSC-projecting ACC neurons.”
From Dissociable roles of prefrontal plasticity in decision-making strategy and execution of habitual behavior (2026) · cites this paper as [39]
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Cites
LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS
Scoville, W. B., & Milner, B. (1957) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.20.1.11 · Cited by 7,322 · see citing works
Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358 · see citing works
Modality-Specific Retrograde Amnesia of Fear
Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483 · see citing works
Context and Behavioral Processes in Extinction: Table 1.
Bouton, M. E. (2004) · Learning & Memory · doi:10.1101/lm.78804 · Cited by 1,808 · see citing works
Differential Effects of Early Hippocampal Pathology on Episodic and Semantic Memory
Vargha-Khadem, F., Gadian, D. G., Watkins, K. E., Connelly, A., Van Paesschen, W., & Mishkin, M. (1997) · Science · doi:10.1126/science.277.5324.376 · Cited by 1,746 · see citing works
Memory consolidation of Pavlovian fear conditioning: a cellular and molecular perspective
Schafe, G. E., Nader, K., Blair, H. T., & LeDoux, J. E. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01969-x · Cited by 510 · see citing works
Reinforcement learning and episodic memory in humans and animals: an integrative framework
Gershman, S. J., & Daw, N. D. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-122414-033625 · Cited by 446 · see citing works
The hippocampus as a cognitive graph.
Muller, R. U., Stead, M., & Pach, J. (1996) · The Journal of general physiology · doi:10.1085/jgp.107.6.663 · Cited by 391 · see citing works
Hippocampal theta sequences reflect current goals
Wikenheiser, A. M., & Redish, A. D. (2015) · Nature Neuroscience · doi:10.1038/nn.3909 · Cited by 367 · see citing works
Russell, W. R., & NATHAN, P. W. (1946) · Brain · doi:10.1093/brain/69.4.280 · Cited by 305 · see citing works
Sequential replay of nonspatial task states in the human hippocampus
Schuck, N. W., & Niv, Y. (2019) · Science · doi:10.1126/science.aaw5181 · Cited by 304 · see citing works
Medial Orbitofrontal Cortex Mediates Outcome Retrieval in Partially Observable Task Situations
Bradfield, L. A., Dezfouli, A., van Holstein, M., Chieng, B. C. H., & Balleine, B. W. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.044 · Cited by 206 · see citing works
Self-citationDickinson, A. (1994) · Animal Learning and Cognition · doi:10.1016/b978-0-08-057169-0.50009-7 · Cited by 200 · see citing works
Contextual control of instrumental actions and habits.
Thrailkill, E. A., & Bouton, M. E. (2015) · Journal of Experimental Psychology: Animal Learning and Cognition · doi:10.1037/xan0000045 · Cited by 165 · see citing works
Hippocampal Contributions to Model-Based Planning and Spatial Memory
Vikbladh, O. M., Meager, M. R., King, J. A., Blackmon, K., Devinsky, O., Shohamy, D., Burgess, N., & Daw, N. D. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.014 · Cited by 152 · see citing works
Anterior hippocampus and goal-directed spatial decision making
Viard, A., Doeller, C. F., Hartley, T., Bird, C. M., & Burgess, N. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4640-10.2011 · Cited by 144 · see citing works
The Role of the Hippocampus in Instrumental Conditioning
Corbit, L. H., & Balleine, B. W. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04233.2000 · Cited by 144 · see citing works
Self-citationGluth, S., Sommer, T., Rieskamp, J., & Büchel, C. (2015) · Neuron · doi:10.1016/j.neuron.2015.04.023 · Cited by 141 · see citing works
The why, what, where, when and how of goal-directed choice: neuronal and computational principles
Verschure, P. F. M. J., Pennartz, C. M. A., & Pezzulo, G. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0483 · Cited by 131 · see citing works
Motivational Control of Instrumental Action
Dickinson, A., & Balleine, B. W. (1995) · Current Directions in Psychological Science · doi:10.1111/1467-8721.ep11512272 · Cited by 116 · see citing works
Self-citationCorbit, L. H., Ostlund, S. B., & Balleine, B. W. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-24-10976.2002 · Cited by 110 · see citing works
Self-citationChoice and contingency in the development of behavioral autonomy during instrumental conditioning.
Kosaki, Y., & Dickinson, A. (2010) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/a0016887 · Cited by 101 · see citing works
Zhou, J., Montesinos-Cartagena, M., Wikenheiser, A. M., Gardner, M., Niv, Y., & Schoenbaum, G. M. (2019) · Current Biology · doi:10.1016/j.cub.2019.08.040 · Cited by 61 · see citing works
Extinction Generates Outcome-Specific Conditioned Inhibition.
Laurent, V., Chieng, B., & Balleine, B. (2016) · Current Biology · doi:10.1016/j.cub.2016.09.021 · Cited by 23 · see citing works
Self-citationEpisodic memory, semantic memory, and amnesia
Squire, L. R., & Zola, S. M. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:3
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Asaoka, N., Pagano, D., & Hayashi, Y. (2026) · Nature Communications · doi:10.1038/s41467-026-75706-1
- Authors
- Bradfield, L. A., Leung, B. K., Boldt, S., Liang, S., & Balleine, B. W.
- Affiliations
- University of Technology Sydney (AU)
- UNSW Sydney (AU)
- The University of Sydney (AU)
- Corresponding author
- Bradfield, Laura A.
- Venue
- Nature Neuroscience
- Published
- 2020-08-10
- Volume
- 23
- Issue
- 10
- Pages
- 1194-1197
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W3048202137
- Cited by
- 65
- References
- 25
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 30 · 2023: 9 · 2022: 11 · 2021: 7 · 2020: 1
- FWCI
- 3.76
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- Locations
- Nature Neuroscience (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- UTS ePRESS (University of Technology Sydney) (submittedVersion)
- OSF Preprints (OSF Preprints) (submittedVersion)
- Funders
- Department of Health | National Health and Medical Research Council (GNT1087689, GNT1148244)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- goal-directed action, dorsal hippocampus, action control, physical context, learning acquisition, rats
- MeSH terms
- Animals, Behavior, Animal, Conditioning, Operant, Female, Goals, Hippocampus, Male, Rats, Long-Evans
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