Evidence map›Paper›PMID 25915477›Full record

ArticleNature neuroscience2015

An acetylcholine-activated microcircuit drives temporal dynamics of cortical activity.

Naiyan Chen, Hiroki Sugihara, Mriganka Sur

Abstract read
In one paragraph

Article in Nature neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers.

0numbers the graph read from it
0cells of the map it votes in
134citing 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

134 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Spatiotemporally dynamic noradrenergic regulation of cortical networks.bioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Brainwide blood volume reflects opposing neural populations.bioRxiv : the preprint server for biology · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Parietal cortex is causally required for state-dependent decisions.bioRxiv : the preprint server for biology · 2025
    Article
  18. Article
  19. Article
  20. Article

74 more citing papers are in PubMed but not listed here.

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

3 authors.

Naiyan Chen *Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Hiroki Sugihara *Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Mriganka SurPicower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Funding

STRUCTURE AND FUNCTION IN THE RETINOGENICULATE PATHWAYR01EY007023 · NEI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUR, MRIGANKA · 1985 to 2018
$5.6M
Cortical representations and plasticity: Neurons and astrocytesR01EY018648 · NEI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SUR, MRIGANKA · 2007 to 2011
$2.5M
Cortical circuits and information flow during memory-guided perceptual decisionsU01NS090473 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SUR, MRIGANKA · 2014 to 2016
$2.4M
NEI NIH HHS R01 EY007023NEI NIH HHS R01EY007023NEI NIH HHS R01 EY018648NEI NIH HHS R01EY018648NINDS NIH HHS U01 NS090473NINDS NIH HHS U01NS090473
6 · The paper itself

Abstract

Cholinergic modulation of cortex powerfully influences information processing and brain states, causing robust desynchronization of local field potentials and strong decorrelation of responses between neurons. We found that intracortical cholinergic inputs to mouse visual cortex specifically and differentially drive a defined cortical microcircuit: they facilitate somatostatin-expressing (SOM) inhibitory neurons that in turn inhibit parvalbumin-expressing inhibitory neurons and pyramidal neurons. Selective optogenetic inhibition of SOM responses blocked desynchronization and decorrelation, demonstrating that direct cholinergic activation of SOM neurons is necessary for this phenomenon. Optogenetic inhibition of vasoactive intestinal peptide-expressing neurons did not block desynchronization, despite these neurons being activated at high levels of cholinergic drive. Direct optogenetic SOM activation, independent of cholinergic modulation, was sufficient to induce desynchronization. Together, these findings demonstrate a mechanistic basis for temporal structure in cortical populations and the crucial role of neuromodulatory drive in specific inhibitory-excitatory circuits in actively shaping the dynamics of neuronal activity.

Indexed as

AcetylcholineAnimalsCerebral CortexCortical SynchronizationExcitatory Postsynaptic PotentialsInterneuronsMiceMice, Inbred C57BLNerve NetNeuronsOptogeneticsParasympathetic Nervous SystemParvalbuminsPhotic StimulationPyramidal CellsSomatostatinAcetylcholineParvalbuminsSomatostatinVasoactive Intestinal Peptide

Identifiers

PMID25915477
PMCPMC4446146

What OpenQuestion holds

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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.