Evidence map›Paper›PMID 25471583›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Optogenetic mapping after stroke reveals network-wide scaling of functional connections and heterogeneous recovery of the peri-infarct.

Diana H Lim, Jeffrey M LeDue, Majid H Mohajerani, Timothy H Murphy

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 115 citations in OpenAlex.

  1. Review
  2. Hemodynamic and Electrophysiological Progression of the Rose Bengal Photothrombotic Stroke Model in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
  4. Article
  5. Astrocytic BEST1 can serve as a target for functional recovery after ischemic stroke.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  6. Neural repair mechanisms after ischemic stroke.Inflammation and regeneration · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Rethinking Remapping: Circuit Mechanisms of Recovery after Stroke.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Peripheral sensory stimulation elicits global slow waves by recruiting somatosensory cortex bilaterally.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  19. Review
  20. Optogenetic Interrogation of Circuits Following Neurotrauma.Frontiers in molecular neuroscience · 2021
    Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Diana H LimDepartment of Psychiatry and.
Jeffrey M LeDueDepartment of Psychiatry and Brain Research Center, University of British Columbia at Vancouver, Vancouver V6T 1Z3, Canada.
Majid H MohajeraniDepartment of Psychiatry and.ORCID http://orcid.org/0000-0003-0964-2977
Timothy H MurphyDepartment of Psychiatry and Brain Research Center, University of British Columbia at Vancouver, Vancouver V6T 1Z3, Canada thmurphy@mail.ubc.ca.
University of British Columbia · CA

Funding

Canadian Institutes of Health Research MOP-111009
6 · The paper itself

Abstract

We used arbitrary point channelrhodopsin-2 (ChR2) stimulation and wide-scale voltage sensitive dye (VSD) imaging in mice to map altered cortical connectivity at 1 and 8 weeks after a targeted cortical stroke. Network analysis based on optogenetic stimulation revealed a symmetrical sham network with distinct sensorimotor and association groupings. This symmetry was disrupted after stroke: at 1 week after stroke, we observed a widespread depression of optogenetically evoked activity that extended to the non-injured hemisphere; by 8 weeks, significant recovery was observed. When we considered the network as a whole, scaling the ChR2-evoked VSD responses from the stroke groups to match the sham group mean resulted in a relative distribution of responses that was indistinguishable from the sham group, suggesting network-wide down-scaling and connectional diaschisis after stroke. Closer inspection revealed that connections that had little connectivity with the peri-infarct, such as contralateral visual areas, tended to escape damage, whereas some connections near the peri-infarct were more severely affected. When connections within the peri-infarct were isolated, we did not observe equal down-scaling of responses after stroke. Peri-infarct sites that had weak connection strength in the sham condition tended to have the greatest relative post-stroke recovery. Our findings suggest that, during recovery, most cortical areas undergo homeostatic upscaling, resulting in a relative distribution of responses that is similar to the pre-stroke (sham) network, albeit still depressed. However, recovery within the peri-infarct zone is heterogeneous and these cortical points do not follow the recovery scaling factor expected for the entire network.

Indexed as

OptogeneticsAnimalsBrain MappingCerebral CortexCerebral InfarctionMaleMiceNeural PathwaysNeuronal PlasticityPhotic StimulationRecovery of Functiondiachisisfunctional recoveryischemiaoptogenetic mappingplasticity

Identifiers

PMID25471583
PMCPMC6608492
OpenAlexW2024835758

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.