Evidence map›Paper›PMID 30018546›Full record

ReviewFrontiers in computational neuroscience2018

Modulation of Spike-Timing Dependent Plasticity: Towards the Inclusion of a Third Factor in Computational Models.

Alexandre Foncelle, Alexandre Mendes, Joanna Jędrzejewska-Szmek, Silvana Valtcheva, Hugues Berry, Kim T Blackwell, Laurent Venance

Abstract readReview
In one paragraph

Review in Frontiers in computational neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Article
  2. Article
  3. Cortical Somatostatin Innervation Follows a Unique Experience-Independent Developmental Trajectory.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Sensory Reinforced Corticostriatal Plasticity.Current neuropharmacology · 2024
    Article
  8. Review
  9. Adaptive control of synaptic plasticity integrates micro- and macroscopic network function.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Brain is modulated by neuronal plasticity during postnatal development.The journal of physiological sciences : JPS · 2021
    Review
  16. Article
  17. 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

7 authors.

Alexandre FoncelleINRIA, Villeurbanne, France.
Alexandre MendesDynamic and Pathophysiology of Neuronal Networks, Center for Interdisciplinary Research in Biology (CIRB), College de France, INSERM U1050, CNRS UMR7241, Labex Memolife, Paris, France.
Joanna Jędrzejewska-SzmekThe Krasnow Institute for Advanced Studies, George Mason University, Fairfax, VA, United States.
Silvana ValtchevaDynamic and Pathophysiology of Neuronal Networks, Center for Interdisciplinary Research in Biology (CIRB), College de France, INSERM U1050, CNRS UMR7241, Labex Memolife, Paris, France.
Hugues BerryINRIA, Villeurbanne, France.
Kim T BlackwellThe Krasnow Institute for Advanced Studies, George Mason University, Fairfax, VA, United States.
Laurent VenanceDynamic and Pathophysiology of Neuronal Networks, Center for Interdisciplinary Research in Biology (CIRB), College de France, INSERM U1050, CNRS UMR7241, Labex Memolife, Paris, France.

Funding

CRCNS: US-French Collaboration: Dopamine modulation of calcium in STDPR01DA038890 · NIDA · GEORGE MASON UNIVERSITY · PI BLACKWELL, KIM L · 2014 to 2017
$637k
NIDA NIH HHS R01 DA038890
6 · The paper itself

Abstract

In spike-timing dependent plasticity (STDP) change in synaptic strength depends on the timing of pre- vs. postsynaptic spiking activity. Since STDP is in compliance with Hebb's postulate, it is considered one of the major mechanisms of memory storage and recall. STDP comprises a system of two coincidence detectors with N-methyl-D-aspartate receptor (NMDAR) activation often posited as one of the main components. Numerous studies have unveiled a third component of this coincidence detection system, namely neuromodulation and glia activity shaping STDP. Even though dopaminergic control of STDP has most often been reported, acetylcholine, noradrenaline, nitric oxide (NO), brain-derived neurotrophic factor (BDNF) or gamma-aminobutyric acid (GABA) also has been shown to effectively modulate STDP. Furthermore, it has been demonstrated that astrocytes, via the release or uptake of glutamate, gate STDP expression. At the most fundamental level, the timing properties of STDP are expected to depend on the spatiotemporal dynamics of the underlying signaling pathways. However in most cases, due to technical limitations experiments grant only indirect access to these pathways. Computational models carefully constrained by experiments, allow for a better qualitative understanding of the molecular basis of STDP and its regulation by neuromodulators. Recently, computational models of calcium dynamics and signaling pathway molecules have started to explore STDP emergence in

Indexed as

acetylcholineastrocytesdopamineeligibility tracesHebbian plasticitynoradrenalineSTDPthird factor

Identifiers

PMID30018546
PMCPMC6037788

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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.