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Hippocampal and orbitofrontal neurons contribute to complementary aspects of associative structure

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  • Huixin Lin

    (Peking University
    Chinese Institute for Brain Research)

  • Jingfeng Zhou

    (Chinese Institute for Brain Research)

Abstract

The ability to establish associations between environmental stimuli is fundamental for higher-order brain functions like state inference and generalization. Both the hippocampus and orbitofrontal cortex (OFC) play pivotal roles in this, demonstrating complex neural activity changes after associative learning. However, how precisely they contribute to representing learned associations remains unclear. Here, we train head-restrained mice to learn four ‘odor-outcome’ sequence pairs composed of several task variables—the past and current odor cues, sequence structure of ‘cue-outcome’ arrangement, and the expected outcome; and perform calcium imaging from these mice throughout learning. Sequence-splitting signals that distinguish between paired sequences are detected in both brain regions, reflecting associative memory formation. Critically, we uncover differential contents in represented associations by examining, in each area, how these task variables affect splitting signal generalization between sequence pairs. Specifically, the hippocampal splitting signals are influenced by the combination of past and current cues that define a particular sensory experience. In contrast, the OFC splitting signals are similar between sequence pairs that share the same sequence structure and expected outcome. These findings suggest that the hippocampus and OFC uniquely and complementarily organize the acquired associative structure.

Suggested Citation

  • Huixin Lin & Jingfeng Zhou, 2024. "Hippocampal and orbitofrontal neurons contribute to complementary aspects of associative structure," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49652-9
    DOI: 10.1038/s41467-024-49652-9
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    References listed on IDEAS

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    1. Jingfeng Zhou & Chunying Jia & Marlian Montesinos-Cartagena & Matthew P. H. Gardner & Wenhui Zong & Geoffrey Schoenbaum, 2021. "Evolving schema representations in orbitofrontal ensembles during learning," Nature, Nature, vol. 590(7847), pages 606-611, February.
    2. Christina M. Gremel & Rui M. Costa, 2013. "Orbitofrontal and striatal circuits dynamically encode the shift between goal-directed and habitual actions," Nature Communications, Nature, vol. 4(1), pages 1-12, October.
    3. Babak Shahbaba & Lingge Li & Forest Agostinelli & Mansi Saraf & Keiland W. Cooper & Derenik Haghverdian & Gabriel A. Elias & Pierre Baldi & Norbert J. Fortin, 2022. "Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    4. Edward H. Nieh & Manuel Schottdorf & Nicolas W. Freeman & Ryan J. Low & Sam Lewallen & Sue Ann Koay & Lucas Pinto & Jeffrey L. Gauthier & Carlos D. Brody & David W. Tank, 2021. "Geometry of abstract learned knowledge in the hippocampus," Nature, Nature, vol. 595(7865), pages 80-84, July.
    5. Ramon Nogueira & Juan M. Abolafia & Jan Drugowitsch & Emili Balaguer-Ballester & Maria V. Sanchez-Vives & Rubén Moreno-Bote, 2017. "Lateral orbitofrontal cortex anticipates choices and integrates prior with current information," Nature Communications, Nature, vol. 8(1), pages 1-13, April.
    6. Raunak Basu & Robert Gebauer & Tim Herfurth & Simon Kolb & Zahra Golipour & Tatjana Tchumatchenko & Hiroshi T. Ito, 2021. "The orbitofrontal cortex maps future navigational goals," Nature, Nature, vol. 599(7885), pages 449-452, November.
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