IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v16y2025i1d10.1038_s41467-025-57119-8.html
   My bibliography  Save this article

Contralesional hippocampal spreading depolarization promotes functional recovery after stroke

Author

Listed:
  • Andrew K. J. Boyce

    (University of Calgary
    University of Calgary
    University of New Mexico Health Sciences Center)

  • Yannick Fouad

    (University of Calgary
    University of Calgary)

  • Renaud C. Gom

    (University of Calgary
    University of Calgary)

  • Donovan M. Ashby

    (University of Calgary
    University of Calgary)

  • Cristina Martins-Silva

    (Federal University of Espírito Santo)

  • Leonardo Molina

    (University of Calgary
    University of Calgary)

  • Tamas Füzesi

    (University of Calgary
    University of Calgary)

  • Carina Ens

    (University of Calgary
    University of Calgary)

  • Wilten Nicola

    (University of Calgary
    University of Calgary)

  • Alexander McGirr

    (University of Calgary
    University of Calgary
    University of Calgary)

  • G. Campbell Teskey

    (University of Calgary
    University of Calgary)

  • Roger J. Thompson

    (University of Calgary
    University of Calgary)

Abstract

Ischemic stroke, brain tissue infarction following obstructed cerebral blood flow, leads to long-term neurological deficits and death. While neocortex is a commonly affected region with established preclinical models, less is known about deeper brain strokes, despite having unique neurological outcomes. We induced focal ischemic stroke while simultaneously monitoring neuronal activity in awake behaving Thy1-GCaMP6f mice by delivering and collecting light through bilateral fiberoptic implants. Unilateral hippocampal stroke resulted in atypical wandering behavior coincident with ipsilesional terminal spreading depolarization (sustained increase in GCaMP6f fluorescence). Ischemia induced seizures that propagated to the contralesional hippocampus triggering a transient spreading depolarization, predominantly in females. Hippocampal stroke impaired contextual fear conditioning acquired pre-stroke. Yet, 7 days post-stroke, contextual fear conditioning was only improved in mice with contralesional spreading depolarization. Blunting peri-stroke contralesional spreading depolarization prevented recovery of hippocampus-dependent learning. Together, we show that regionally isolated deleterious and beneficial spreading depolarizations can occur concurrently in the murine brain during acute stroke.

Suggested Citation

  • Andrew K. J. Boyce & Yannick Fouad & Renaud C. Gom & Donovan M. Ashby & Cristina Martins-Silva & Leonardo Molina & Tamas Füzesi & Carina Ens & Wilten Nicola & Alexander McGirr & G. Campbell Teskey & R, 2025. "Contralesional hippocampal spreading depolarization promotes functional recovery after stroke," Nature Communications, Nature, vol. 16(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57119-8
    DOI: 10.1038/s41467-025-57119-8
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-025-57119-8
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-025-57119-8?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Franziska Bender & Maria Gorbati & Marta Carus Cadavieco & Natalia Denisova & Xiaojie Gao & Constance Holman & Tatiana Korotkova & Alexey Ponomarenko, 2015. "Theta oscillations regulate the speed of locomotion via a hippocampus to lateral septum pathway," Nature Communications, Nature, vol. 6(1), pages 1-11, December.
    2. Tamás Füzesi & Nuria Daviu & Jaclyn I. Wamsteeker Cusulin & Robert P. Bonin & Jaideep S. Bains, 2016. "Hypothalamic CRH neurons orchestrate complex behaviours after stress," Nature Communications, Nature, vol. 7(1), pages 1-14, September.
    3. Isra Tamim & David Y. Chung & Andreia Lopes Morais & Inge C. M. Loonen & Tao Qin & Amrit Misra & Frieder Schlunk & Matthias Endres & Steven J. Schiff & Cenk Ayata, 2021. "Spreading depression as an innate antiseizure mechanism," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
    4. Elliot H. Smith & Jyun-you Liou & Tyler S. Davis & Edward M. Merricks & Spencer S. Kellis & Shennan A. Weiss & Bradley Greger & Paul A. House & Guy M. McKhann II & Robert R. Goodman & Ronald G. Emerso, 2016. "The ictal wavefront is the spatiotemporal source of discharges during spontaneous human seizures," Nature Communications, Nature, vol. 7(1), pages 1-12, September.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. John-Sebastian Mueller & Fabio C. Tescarollo & Trong Huynh & Daniel A. Brenner & Daniel J. Valdivia & Kanyin Olagbegi & Sahana Sangappa & Spencer C. Chen & Hai Sun, 2023. "Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    2. Joshua M. Diamond & Julio I. Chapeton & Weizhen Xie & Samantha N. Jackson & Sara K. Inati & Kareem A. Zaghloul, 2024. "Focal seizures induce spatiotemporally organized spiking activity in the human cortex," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    3. Vasiliki Bougou & Michaël Vanhoyland & Alexander Bertrand & Wim Paesschen & Hans Op De Beeck & Peter Janssen & Tom Theys, 2024. "Neuronal tuning and population representations of shape and category in human visual cortex," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    4. Guillaume Etter & Suzanne Veldt & Jisoo Choi & Sylvain Williams, 2023. "Optogenetic frequency scrambling of hippocampal theta oscillations dissociates working memory retrieval from hippocampal spatiotemporal codes," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    5. Solomiia Korchynska & Patrick Rebernik & Marko Pende & Laura Boi & Alán Alpár & Ramon Tasan & Klaus Becker & Kira Balueva & Saiedeh Saghafi & Peer Wulff & Tamas L. Horvath & Gilberto Fisone & Hans-Ulr, 2022. "A hypothalamic dopamine locus for psychostimulant-induced hyperlocomotion in mice," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    6. Xiangling Feng & Yingjie Gao & Fan Chu & Yuwen Shan & Meicheng Liu & Yaoyi Wang & Ying Zhu & Qing Lu & Mingfeng Li, 2025. "Cortical arealization of interneurons defines shared and distinct molecular programs in developing human and macaque brains," Nature Communications, Nature, vol. 16(1), pages 1-18, December.
    7. Anton V Chizhov & Aleksei E Sanin, 2020. "A simple model of epileptic seizure propagation: Potassium diffusion versus axo-dendritic spread," PLOS ONE, Public Library of Science, vol. 15(4), pages 1-21, April.
    8. Tamás Füzesi & Neilen P. Rasiah & David G. Rosenegger & Mijail Rojas-Carvajal & Taylor Chomiak & Núria Daviu & Leonardo A. Molina & Kathryn Simone & Toni-Lee Sterley & Wilten Nicola & Jaideep S. Bains, 2023. "Hypothalamic CRH neurons represent physiological memory of positive and negative experience," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    9. Blake J. Laham & Sahana S. Murthy & Monica Hanani & Mona Clappier & Sydney Boyer & Betsy Vasquez & Elizabeth Gould, 2022. "The estrous cycle modulates early-life adversity effects on mouse avoidance behavior through progesterone signaling," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    10. Paula Gómez-Sotres & Urszula Skupio & Tommaso Dalla Tor & Francisca Julio-Kalajzic & Astrid Cannich & Doriane Gisquet & Itziar Bonilla-Del Rio & Filippo Drago & Nagore Puente & Pedro Grandes & Luigi B, 2024. "Olfactory bulb astrocytes link social transmission of stress to cognitive adaptation in male mice," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    11. Pierre Bourdillon & Liankun Ren & Mila Halgren & Angelique C. Paulk & Pariya Salami & István Ulbert & Dániel Fabó & Jean-Rémi King & Kane M. Sjoberg & Emad N. Eskandar & Joseph R. Madsen & Eric Halgre, 2024. "Differential cortical layer engagement during seizure initiation and spread in humans," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    12. Predrag Jovanovic & Allan-Hermann Pool & Nancy Morones & Yidan Wang & Edward Novinbakht & Nareg Keshishian & Kaitlyn Jang & Yuki Oka & Celine E. Riera, 2023. "A sex-specific thermogenic neurocircuit induced by predator smell recruiting cholecystokinin neurons in the dorsomedial hypothalamus," Nature Communications, Nature, vol. 14(1), pages 1-19, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57119-8. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.