Temporal dynamics of Purkinje cell-intrinsic excitability governs cerebellar systems consolidation

Systems consolidation reorganizes newly encoded memories from cortical networks into downstream circuits. Although synaptic mechanisms are extensively characterized, the role of neuronal intrinsic excitability (IE) in this process remains relatively unexplored. Here, we utilized a cerebellum-dependent learning model to investigate the causal link between neuronal IE and memory consolidation. The optogenetic manipulation of Purkinje cells (PCs), the sole output of the cerebellar cortex, identified a crucial 90-min post-learning window during which PC-IE undergoes transient depression. Disrupting this decline by elevating PC-IE hindered long-term memory, whereas interventions outside this window did not. Elevated PC-IE spared basal ocular reflexes, indicating its role is specific to adaptive consolidation states. Moreover, increased PC-IE abolished learning-induced intrinsic plasticity in flocculus-targeting neurons (FTNs) of the medial vestibular nucleus (MVN), a downstream locus for persisting memory storage. These findings underscore the precise temporal dynamics of IE as a critical mechanism in systems consolidation, emphasizing its vulnerability to disruptions.

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Publication Details

Journal
iScience
Published
2025-10-15
DOI
https://doi.org/10.1016/j.isci.2025.113760
Primary Topic
Vestibular and auditory disorders
Type
article
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article

Temporal dynamics of Purkinje cell-intrinsic excitability governs cerebellar systems consolidation

Jewoo Seo, Yong Gyu Kim, Sang Jeong Kim, Yong‐Seok Lee
iScience
Vestibular and auditory disorders
article

Temporal dynamics of Purkinje cell-intrinsic excitability governs cerebellar systems consolidation

Jewoo Seo, Yong Gyu Kim, Sang Jeong Kim, Yong‐Seok Lee
article en

Abstract

Systems consolidation reorganizes newly encoded memories from cortical networks into downstream circuits. Although synaptic mechanisms are extensively characterized, the role of neuronal intrinsic excitability (IE) in this process remains relatively unexplored. Here, we utilized a cerebellum-dependent learning model to investigate the causal link between neuronal IE and memory consolidation. The optogenetic manipulation of Purkinje cells (PCs), the sole output of the cerebellar cortex, identified a crucial 90-min post-learning window during which PC-IE undergoes transient depression. Disrupting this decline by elevating PC-IE hindered long-term memory, whereas interventions outside this window did not. Elevated PC-IE spared basal ocular reflexes, indicating its role is specific to adaptive consolidation states. Moreover, increased PC-IE abolished learning-induced intrinsic plasticity in flocculus-targeting neurons (FTNs) of the medial vestibular nucleus (MVN), a downstream locus for persisting memory storage. These findings underscore the precise temporal dynamics of IE as a critical mechanism in systems consolidation, emphasizing its vulnerability to disruptions.

iScienceVol. 28(11)
Seoul National University (KR), National University College (PR)
Openalex Percentile: Top 63%
Vestibular and auditory disorders
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