Evidence map›Paper›PMID 29042433›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

Serotonin Decreases the Gain of Visual Responses in Awake Macaque V1.

Lenka Seillier, Corinna Lorenz, Katsuhisa Kawaguchi, Torben Ott, Andreas Nieder, Paria Pourriahi, Hendrikje Nienborg

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Negative affect interacts with perceptual affective biases.Journal of psychopharmacology (Oxford, England) · 2026
    Article
  3. Repeated restraint stress enhances visual plasticity through locus coeruleus (LC)-V1 projection in adult mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
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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

7 authors at 3 institutions in 3 countries.

Lenka SeillierWerner Reichardt Centre for Integrative Neuroscience and.
Corinna LorenzWerner Reichardt Centre for Integrative Neuroscience and.
Katsuhisa KawaguchiWerner Reichardt Centre for Integrative Neuroscience and.
Torben OttDepartment of Animal Physiology, Institute of Neurobiology, University of Tübingen, 72076 Tübingen, Germany.
Andreas NiederWerner Reichardt Centre for Integrative Neuroscience and.ORCID 0000-0001-6381-0375
Paria PourriahiWerner Reichardt Centre for Integrative Neuroscience and.
Hendrikje NienborgWerner Reichardt Centre for Integrative Neuroscience and hendrikje.nienborg@cin.uni-tuebingen.de.ORCID 0000-0002-2167-7251
Integrative Medicine Institute · USUniversity Graduate Center · NOUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serotonin, an important neuromodulator in the brain, is implicated in affective and cognitive functions. However, its role even for basic cortical processes is controversial. For example, in the mammalian primary visual cortex (V1), heterogenous serotonergic modulation has been observed in anesthetized animals. Here, we combined extracellular single-unit recordings with iontophoresis in awake animals. We examined the role of serotonin on well-defined tuning properties (orientation, spatial frequency, contrast, and size) in V1 of two male macaque monkeys. We find that in the awake macaque the modulatory effect of serotonin is surprisingly uniform: it causes a mainly multiplicative decrease of the visual responses and a slight increase in the stimulus-selective response latency. Moreover, serotonin neither systematically changes the selectivity or variability of the response, nor the interneuronal correlation unexplained by the stimulus ("noise-correlation"). The modulation by serotonin has qualitative similarities with that for a decrease in stimulus contrast, but differs quantitatively from decreasing contrast. It can be captured by a simple additive change to a threshold-linear spiking nonlinearity. Together, our results show that serotonin is well suited to control the response gain of neurons in V1 depending on the animal's behavioral or motivational context, complementing other known state-dependent gain-control mechanisms.

Indexed as

Evoked Potentials, VisualAnimalsIontophoresisMacaca mulattaMaleReaction TimeSerotoninVisual CortexWakefulnessSerotoninawake macaqueextracellular recordingsgain modulationiontophoresisserotoninstriate cortex

Identifiers

PMID29042433
PMCPMC5700422
OpenAlexW2766850030

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.