Evidence map›Paper›PMID 27233469›Full record

ArticleThe European journal of neuroscience2017

Calcium dynamics predict direction of synaptic plasticity in striatal spiny projection neurons.

Joanna Jędrzejewska-Szmek, Sriraman Damodaran, Daniel B Dorman, Kim T Blackwell

Open access · greenAbstract read
In one paragraph

Article in The European journal of neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Enhancement of calcium responses by KJournal of biosciences · 2026
    Article
  4. Review
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  6. Heterosynaptic plasticity-induced modulation of synapses.The journal of physiological sciences : JPS · 2023
    Review
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  20. Thinking Outside the Box (and Arrow): Current Themes in Striatal Dysfunction in Movement Disorders.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2019
    Review
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

4 authors at 2 institutions in 1 country.

Joanna Jędrzejewska-SzmekThe Krasnow Institute for Advanced Study, George Mason University, Fairfax, VA, 22030, USA.
Sriraman DamodaranThe Krasnow Institute for Advanced Study, George Mason University, Fairfax, VA, 22030, USA.
Daniel B DormanThe Krasnow Institute for Advanced Study, George Mason University, Fairfax, VA, 22030, USA.
Kim T BlackwellThe Krasnow Institute for Advanced Study, George Mason University, Fairfax, VA, 22030, USA.
George Mason University · USInstitute for Advanced Study · US

Funding

mTOR, a new target for opioid-induced tolerance and hyperalgesiaR01DA033390 · NIDA · RBHS-NEW JERSEY MEDICAL SCHOOL · PI TAO, YUAN-XIANG · 2013 to 2017
$1.8M
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 DA033390NIDA NIH HHS R01 DA038890
6 · The paper itself

Abstract

The striatum is a major site of learning and memory formation for sensorimotor and cognitive association. One of the mechanisms used by the brain for memory storage is synaptic plasticity - the long-lasting, activity-dependent change in synaptic strength. All forms of synaptic plasticity require an elevation in intracellular calcium, and a common hypothesis is that the amplitude and duration of calcium transients can determine the direction of synaptic plasticity. The utility of this hypothesis in the striatum is unclear in part because dopamine is required for striatal plasticity and in part because of the diversity in stimulation protocols. To test whether calcium can predict plasticity direction, we developed a calcium-based plasticity rule using a spiny projection neuron model with sophisticated calcium dynamics including calcium diffusion, buffering and pump extrusion. We utilized three spike timing-dependent plasticity (STDP) induction protocols, in which postsynaptic potentials are paired with precisely timed action potentials and the timing of such pairing determines whether potentiation or depression will occur. Results show that despite the variation in calcium dynamics, a single, calcium-based plasticity rule, which explicitly considers duration of calcium elevations, can explain the direction of synaptic weight change for all three STDP protocols. Additional simulations show that the plasticity rule correctly predicts the NMDA receptor dependence of long-term potentiation and the L-type channel dependence of long-term depression. By utilizing realistic calcium dynamics, the model reveals mechanisms controlling synaptic plasticity direction, and shows that the dynamics of calcium, not just calcium amplitude, are crucial for synaptic plasticity.

Indexed as

Models, NeurologicalAnimalsCalciumCalcium Channels, L-TypeComputer SimulationCorpus StriatumDiffusionFemaleMaleMembrane PotentialsNeural InhibitionNeural PathwaysNeuronal PlasticityNeuronsNeurotransmitter AgentsReceptors, AMPACalciumCalcium Channels, L-TypeNeurotransmitter AgentsReceptors, AMPAReceptors, GABA-AReceptors, N-Methyl-D-Aspartatebasal gangliacomputational modellong-term potentiation/long-term depressionspike timing-dependent plasticitystriatum

Identifiers

PMID27233469
PMCPMC5124545
OpenAlexW2399650551

What OpenQuestion holds

Textmetadata
LicenceTDM
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.