Evidence map›Paper›PMID 31366632›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Rapid and active stabilization of visual cortical firing rates across light-dark transitions.

Alejandro Torrado Pacheco, Elizabeth I Tilden, Sophie M Grutzner, Brian J Lane, Yue Wu, Keith B Hengen, Julijana Gjorgjieva, Gina G Turrigiano

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Modular arrangement of synaptic and intrinsic homeostatic plasticity within visual cortical circuits.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Blockade of GluN2B-Containing NMDA Receptors Prevents Potentiation and Depression of Responses during Ocular Dominance Plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  8. Visual Deprivation during Mouse Critical Period Reorganizes Network-Level Functional Connectivity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  9. Article
  10. Amyloid Pathology Impairs Experience-Dependent Inhibitory Synaptic Plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  11. Article
  12. Article
  13. Induction of Activity-Dependent Plasticity at Auditory Nerve Synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  14. Article
  15. Article
  16. Local dendritic balance enables learning of efficient representations in networks of spiking neurons.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Developmental Regulation of Homeostatic Plasticity in Mouse Primary Visual Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Alejandro Torrado PachecoDepartment of Biology, Brandeis University, Waltham, MA 02453.
Elizabeth I TildenDepartment of Biology, Brandeis University, Waltham, MA 02453.
Sophie M GrutznerDepartment of Biology, Brandeis University, Waltham, MA 02453.
Brian J LaneDepartment of Biology, Brandeis University, Waltham, MA 02453.
Yue WuComputation in Neural Circuits Group, Max Planck Institute for Brain Research, 60438 Frankfurt, Germany.
Keith B HengenDepartment of Biology, Brandeis University, Waltham, MA 02453.
Julijana GjorgjievaComputation in Neural Circuits Group, Max Planck Institute for Brain Research, 60438 Frankfurt, Germany.ORCID 0000-0001-7118-4079
Gina G TurrigianoDepartment of Biology, Brandeis University, Waltham, MA 02453; turrigiano@brandeis.edu.

Funding

Quantitative Neuroscience: Tools for Bridging Levels of AnalysisT32NS007292 · NINDS · BRANDEIS UNIVERSITY · PI GINA G TURRIGIANO · 1986 to 2026
$12.7M
Mechanisms and Function of Firing Rate Homeostasis in Cortical CircuitsR35NS111562 · NINDS · BRANDEIS UNIVERSITY · PI GINA G TURRIGIANO · 2019 to 2026
$7.3M
Gating of Firing Rate Homeostasis by Sleep and Wake States During Experience-Dependent PlasticityR01EY025613 · NEI · BRANDEIS UNIVERSITY · PI TURRIGIANO, GINA G · 2017 to 2025
$3.9M
Undergraduate and Graduate Training in Computational Neuroscience R90DA033463 · NIDA · BRANDEIS UNIVERSITY · PI MILLER, PAUL · 2011 to 2020
$2.0M
Homeostatic plasticity mechanisms support brain function in vivoK99NS089800 · NINDS · BRANDEIS UNIVERSITY · PI HENGEN, KEITH B. · 2014 to 2015
$161k
NEI NIH HHS R01 EY025613NIDA NIH HHS R90 DA033463NINDS NIH HHS K99 NS089800NINDS NIH HHS R35 NS111562NINDS NIH HHS T32 NS007292
6 · The paper itself

Abstract

The dynamics of neuronal firing during natural vision are poorly understood. Surprisingly, mean firing rates of neurons in primary visual cortex (V1) of freely behaving rodents are similar during prolonged periods of light and darkness, but it is unknown whether this reflects a slow adaptation to changes in natural visual input or insensitivity to rapid changes in visual drive. Here, we use chronic electrophysiology in freely behaving rats to follow individual V1 neurons across many dark-light (D-L) and light-dark (L-D) transitions. We show that, even on rapid timescales (1 s to 10 min), neuronal activity was only weakly modulated by transitions that coincided with the expected 12-/12-h L-D cycle. In contrast, a larger subset of V1 neurons consistently responded to unexpected L-D and D-L transitions, and disruption of the regular L-D cycle with 60 h of complete darkness induced a robust increase in V1 firing on reintroduction of visual input. Thus, V1 neurons fire at similar rates in the presence or absence of natural stimuli, and significant changes in activity arise only transiently in response to unexpected changes in the visual environment. Furthermore, although mean rates were similar in light and darkness, pairwise correlations were significantly stronger during natural vision, suggesting that information about natural scenes in V1 may be more strongly reflected in correlations than individual firing rates. Together, our findings show that V1 firing rates are rapidly and actively stabilized during expected changes in visual input and are remarkably stable at both short and long timescales.

Indexed as

DarknessPhotic StimulationAction PotentialsAnimalsFemaleMaleRatsRats, Long-EvansVisual CortexVisual Perceptionfiring-rate stabilityrodent visionvisual cortexvisual experience

Identifiers

PMID31366632
PMCPMC6731644

What OpenQuestion holds

Textmetadata
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Registered trials

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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.