Evidence map›Paper›PMID 31527242›Full record

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

Cell class-specific modulation of attentional signals by acetylcholine in macaque frontal eye field.

Miguel Dasilva, Christian Brandt, Sascha Gotthardt, Marc Alwin Gieselmann, Claudia Distler, Alexander Thiele

Open access · hybridAbstract 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 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
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  8. Neuroanatomical Substrates of Circuit-Specific Cholinergic Modulation across the Primate Anterior Cingulate Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  9. Cholinergic Neuromodulation of Prefrontal Attractor Dynamics Controls Performance in Spatial Working Memory.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  10. Article
  11. Article
  12. Pathway-selective optogenetics reveals the functional anatomy of top-down attentional modulation in the macaque visual cortex.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Review
  14. MProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. Ripples in macaque V1 and V4 are modulated by top-down visual attention.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  19. Review
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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

6 authors at 2 institutions in 2 countries.

Miguel DasilvaInstitute of Neuroscience, Newcastle University, Newcastle upon Tyne, NE2 4HH, United Kingdom.
Christian BrandtInstitute of Neuroscience, Newcastle University, Newcastle upon Tyne, NE2 4HH, United Kingdom.ORCID 0000-0003-0672-9487
Sascha GotthardtInstitute of Neuroscience, Newcastle University, Newcastle upon Tyne, NE2 4HH, United Kingdom.
Marc Alwin GieselmannInstitute of Neuroscience, Newcastle University, Newcastle upon Tyne, NE2 4HH, United Kingdom.
Claudia DistlerAllgemeine Zoologie und Neurobiologie, Ruhr-Universität Bochum, 44801 Bochum, Germany.
Alexander ThieleInstitute of Neuroscience, Newcastle University, Newcastle upon Tyne, NE2 4HH, United Kingdom; alex.thiele@ncl.ac.uk.ORCID 0000-0003-4894-0213
Newcastle University · GBRuhr University Bochum · DE

Funding

Biotechnology and Biological Sciences Research Council BB/F021399/1Medical Research Council MR/K013785/1Medical Research Council MR/P013031/1Wellcome Trust 093104
6 · The paper itself

Abstract

Attention is critical to high-level cognition, and attentional deficits are a hallmark of cognitive dysfunction. A key transmitter for attentional control is acetylcholine, but its cellular actions in attention-controlling areas remain poorly understood. Here we delineate how muscarinic and nicotinic receptors affect basic neuronal excitability and attentional control signals in different cell types in macaque frontal eye field. We found that broad spiking and narrow spiking cells both require muscarinic and nicotinic receptors for normal excitability, thereby affecting ongoing or stimulus-driven activity. Attentional control signals depended on muscarinic, not nicotinic receptors in broad spiking cells, while they depended on both muscarinic and nicotinic receptors in narrow spiking cells. Cluster analysis revealed that muscarinic and nicotinic effects on attentional control signals were highly selective even for different subclasses of narrow spiking cells and of broad spiking cells. These results demonstrate that cholinergic receptors are critical to establish attentional control signals in the frontal eye field in a cell type-specific manner.

Indexed as

Signal TransductionAcetylcholineAction PotentialsAnimalsAttentionFrontal LobeMacaca mulattaNeuronsReceptors, CholinergicReceptors, MuscarinicAcetylcholineReceptors, CholinergicReceptors, Muscarinicacetylcholineattentionfrontal cortex

Identifiers

PMID31527242
PMCPMC6778228
OpenAlexW2969369763

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.