Skip to content
DraconiticResearch
Search Sources API
203,948 studies31 sourcesUpdated 22 min ago
PreprintCC BY-NC-NDbioRxiv

A Novel Cortico-Striatal NREM Sleep Rhythm in Mice and Non-Human Primates

  1. 1University of California, San Francisco

Abstract

With practice, rapid early gains in performance are followed by a slower phase marked by kinematic refinement, automaticity and enhanced cortical and striatal interactions. While sleep is known to support early learning, its causal role in the slow phase of learning is not known. Here we recorded neuronal activity in primary motor cortex (M1) and the dorsolateral striatum (DLS) during long-term skill acquisition and interleaved sleep. Surprisingly, the slow phase of learning was marked by the emergence of a previously unrecognized 5-10 Hz oscillatory activity during NREM sleep that was coherent across M1 and DLS. This oscillation resulted in repeated joint reactivation of task-specific information in cortex and striatum. Strikingly, during later stages of training, such joint reactivation of task activity increased over the course of NREM sleep, suggesting that sleep-dependent processing strengthens cortico-striatal interactions. The strength of M1-DLS coherence was predictive of next-day performance gains and increased cortico-striatal coupling during task performance. Targeted closed-loop disruption of this oscillation during NREM sleep abolished performance gains, whereas switching to a dose matched random stimulation paradigm enabled performance improvements in the same animals. Importantly, the same cortico-striatal 5-10 Hz rhythm was also found in sleeping non-human primates, where it was selectively enhanced following learning. Together, we identify, across species, a novel NREM sleep oscillation that is important for sleep-dependent performance gains which depend on cortico-striatal processing.

Related

  1. Neuroimmune remodeling of cortico-striatal circuits in pediatric Tourette syndrome: from immune-to-brain signaling to inhibitory network dysfunction
    Yuchen Hu, Cao Gong, Fei Fan +2
    Frontiers in ImmunologyPeer-reviewedCC BY 4.0ImmunologyCrossref
  2. INS-fMRI: a novel method for mapping mesoscale connectome networks in vivo in nonhuman primates
    X. Du, J. Wang, Y. Zhang +6
    bioRxivPreprintAll rights reservedFull textNeurosciencebioRxiv
  3. A novel methodology for assessing reinforcement choice in primates under human care
    M. I. Leiva, R. K. Griffin, T. R. Lewis
    bioRxivPreprintCC BY-NC-NDFull textZoology & animal behaviourbioRxiv
  4. Parkinsonism with Reduced Striatal Uptake on DAT-SPECT in a Patient Harboring a Novel KCND3 Variant.
    Kimitaka Katanazaka, Mariko Takata, China Kanai +8
    Cerebellum (London, England)Peer-reviewedCC BY-NC-NDFull textNeuroscienceEurope PMC
  5. An in silico cortico-basal ganglia-thalamic testbed for comparing visual and deep brain stimulation in Parkinson’s disease
    Chun-Hui Huang, Wen-Shuo Chen, Jin-Rong Lai +4
    Frontiers in computational neurosciencePeer-reviewedCC BYFull textNeuroscienceEurope PMC
BibTeX
@misc{mizrahikliger2026novel,
  title = {{A Novel Cortico-Striatal NREM Sleep Rhythm in Mice and Non-Human Primates}},
  author = {A. D. Mizrahi-Kliger and S. Coury and C. L. Woodard and K. Ganguly},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.11.750712},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.11.750712v1},
  note = {CC BY-NC-ND},
}
RIS
TY  - UNPB
TI  - A Novel Cortico-Striatal NREM Sleep Rhythm in Mice and Non-Human Primates
AU  - A. D. Mizrahi-Kliger
AU  - S. Coury
AU  - C. L. Woodard
AU  - K. Ganguly
PY  - 2026
DA  - 2026/09/11
PB  - bioRxiv
DO  - 10.64898/2026.09.11.750712
UR  - https://www.biorxiv.org/content/10.64898/2026.09.11.750712v1
AB  - With practice, rapid early gains in performance are followed by a slower phase marked by kinematic refinement, automaticity and enhanced cortical and striatal interactions. While sleep is known to support early learning, its causal role in the slow phase of learning is not known. Here we recorded neuronal activity in primary motor cortex (M1) and the dorsolateral striatum (DLS) during long-term skill acquisition and interleaved sleep. Surprisingly, the slow phase of learning was marked by the emergence of a previously unrecognized 5-10 Hz oscillatory activity during NREM sleep that was coherent across M1 and DLS. This oscillation resulted in repeated joint reactivation of task-specific information in cortex and striatum. Strikingly, during later stages of training, such joint reactivation of task activity increased over the course of NREM sleep, suggesting that sleep-dependent processing strengthens cortico-striatal interactions. The strength of M1-DLS coherence was predictive of next-day performance gains and increased cortico-striatal coupling during task performance. Targeted closed-loop disruption of this oscillation during NREM sleep abolished performance gains, whereas switching to a dose matched random stimulation paradigm enabled performance improvements in the same animals. Importantly, the same cortico-striatal 5-10 Hz rhythm was also found in sleeping non-human primates, where it was selectively enhanced following learning. Together, we identify, across species, a novel NREM sleep oscillation that is important for sleep-dependent performance gains which depend on cortico-striatal processing.
ER  -