Evidence map›Paper›PMID 30485271›Full record

ArticlePloS one2018

Zinc enhances hippocampal long-term potentiation at CA1 synapses through NR2B containing NMDA receptors.

John A Sullivan, Xiao-Lei Zhang, Arthur P Sullivan, Linnea R Vose, Alexander A Moghadam, Victor A Fried, Patric K Stanton

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Crosstalk of copper and zinc in the pathogenesis of vascular dementia.Journal of clinical biochemistry and nutrition · 2022
    Article
  5. Review
  6. Article
  7. Effects of Exercise on Long-Term Potentiation in Neuropsychiatric Disorders.Advances in experimental medicine and biology · 2020
    Review
  8. Article
  9. 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 at 2 institutions in 1 country.

John A SullivanCell Biology & Anatomy, New York Medical College, Valhalla, New York, United States of America.ORCID 0000-0001-7128-271X
Xiao-Lei ZhangCell Biology & Anatomy, New York Medical College, Valhalla, New York, United States of America.
Arthur P SullivanPsychology & Education, Touro School of Health Sciences, New York, New York, United States of America.ORCID 0000-0002-8880-4446
Linnea R VoseCell Biology & Anatomy, New York Medical College, Valhalla, New York, United States of America.
Alexander A MoghadamCell Biology & Anatomy, New York Medical College, Valhalla, New York, United States of America.
Victor A FriedCell Biology & Anatomy, New York Medical College, Valhalla, New York, United States of America.
Patric K StantonCell Biology & Anatomy, New York Medical College, Valhalla, New York, United States of America.
New York Medical College · USTouro College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of zinc (Zn2+), a modulator of N-methyl-D-aspartate (NMDA) receptors, in regulating long-term synaptic plasticity at hippocampal CA1 synapses is poorly understood. The effects of exogenous application of Zn2+ and of chelation of endogenous Zn2+ were examined on long-term potentiation (LTP) of stimulus-evoked synaptic transmission at Schaffer collateral (SCH) synapses in field CA1 of mouse hippocampal slices using whole-cell patch clamp and field recordings. Low micromolar concentrations of exogenous Zn2+ enhanced the induction of LTP, and this effect required activation of NMDA receptors containing NR2B subunits. Zn2+ elicited a selective increase in NMDA/NR2B fEPSPs, and removal of endogenous Zn2+ with high-affinity Zn2+ chelators robustly reduced the magnitude of stimulus-evoked LTP. Taken together, our data show that Zn2+ at physiological concentrations enhances activation of NMDA receptors containing NR2B subunits, and that this effect enhances the magnitude of LTP.

Indexed as

AnimalsCA1 Region, HippocampalChelating AgentsExcitatory Postsynaptic PotentialsLong-Term PotentiationMice, Inbred C57BLProtein Kinase InhibitorsPyramidal CellsReceptors, N-Methyl-D-Aspartatesrc-Family KinasesSynapsesZincChelating AgentsNR2B NMDA receptorProtein Kinase InhibitorsReceptors, N-Methyl-D-Aspartatesrc-Family KinasesZinc

Identifiers

PMID30485271
PMCPMC6261414
OpenAlexW2903470223

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.