Author
Listed:
- Alexander C. W. Smith
(Icahn School of Medicine at Mount Sinai)
- Sietse Jonkman
(Icahn School of Medicine at Mount Sinai)
- Alexandra G. Difeliceantonio
(Icahn School of Medicine at Mount Sinai
Fralin Biomedical Research Institute)
- Richard M. O’Connor
(Icahn School of Medicine at Mount Sinai)
- Soham Ghoshal
(Icahn School of Medicine at Mount Sinai
City University of New York)
- Michael F. Romano
(Boston University)
- Barry J. Everitt
(University of Cambridge)
- Paul J. Kenny
(Icahn School of Medicine at Mount Sinai)
Abstract
Comparatively little is known about how new instrumental actions are encoded in the brain. Using whole-brain c-Fos mapping, we show that neural activity is increased in the anterior dorsolateral striatum (aDLS) of mice that successfully learn a new lever-press response to earn food rewards. Post-learning chemogenetic inhibition of aDLS disrupts consolidation of the new instrumental response. Similarly, post-learning infusion of the protein synthesis inhibitor anisomycin into the aDLS disrupts consolidation of the new response. Activity of D1 receptor-expressing medium spiny neurons (D1-MSNs) increases and D2-MSNs activity decreases in the aDLS during consolidation. Chemogenetic inhibition of D1-MSNs in aDLS disrupts the consolidation process whereas D2-MSN inhibition strengthens consolidation but blocks the expression of previously learned habit-like responses. These findings suggest that D1-MSNs in the aDLS encode new instrumental actions whereas D2-MSNs oppose this new learning and instead promote expression of habitual actions.
Suggested Citation
Alexander C. W. Smith & Sietse Jonkman & Alexandra G. Difeliceantonio & Richard M. O’Connor & Soham Ghoshal & Michael F. Romano & Barry J. Everitt & Paul J. Kenny, 2021.
"Opposing roles for striatonigral and striatopallidal neurons in dorsolateral striatum in consolidating new instrumental actions,"
Nature Communications, Nature, vol. 12(1), pages 1-16, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25460-3
DOI: 10.1038/s41467-021-25460-3
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