Evidence map›Paper›PMID 32093363›Full record

ArticleInternational journal of molecular sciences2020

Developmental Time Course of SNAP-25 Isoforms Regulate Hippocampal Long-Term Synaptic Plasticity and Hippocampus-Dependent Learning.

Katisha R Gopaul, Muhammad Irfan, Omid Miry, Linnea R Vose, Alexander Moghadam, Galadu Subah, Tomas Hökfelt, Christina Bark, Patric K Stanton

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. 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, 15 citations in OpenAlex.

  1. Isoswitching drives the aging process in human brains.bioRxiv : the preprint server for biology · 2025
    Article
  2. Adenylyl Cyclases as Therapeutic Targets in Neuroregeneration.International journal of molecular sciences · 2025
    Review
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  5. The Role ofInternational journal of molecular sciences · 2023
    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

9 authors at 2 institutions in 2 countries.

Katisha R GopaulDepartment of Cell Biology & Anatomy, New York Medical College, Valhalla, NY 10595, USA.
Muhammad IrfanDepartment of Cell Biology & Anatomy, New York Medical College, Valhalla, NY 10595, USA.
Omid MiryDepartment of Cell Biology & Anatomy, New York Medical College, Valhalla, NY 10595, USA.
Linnea R VoseDepartment of Cell Biology & Anatomy, New York Medical College, Valhalla, NY 10595, USA.
Alexander MoghadamDepartment of Cell Biology & Anatomy, New York Medical College, Valhalla, NY 10595, USA.
Galadu SubahDepartment of Cell Biology & Anatomy, New York Medical College, Valhalla, NY 10595, USA.
Tomas HökfeltDepartment of Neuroscience, Karolinska Institutet, 171 77 Stockholm, Sweden.
Christina BarkDepartment of Neuroscience, Karolinska Institutet, 171 77 Stockholm, Sweden.
Patric K StantonDepartment of Cell Biology & Anatomy, New York Medical College, Valhalla, NY 10595, USA.ORCID 0000-0002-2294-0613
New York Medical College · USKarolinska Institutet · SE

Funding

Åhlén-stiftelsen N/ADemensfonden N/ANIH HHS NRSANIH HHS NS044421Stiftelsen för Gamla Tjänarinnor N/ASven Mattssons Stiftelsen N/ASvenska Forskningsrådet Formas N/A
6 · The paper itself

Abstract

SNAP-25 is essential to activity-dependent vesicle fusion and neurotransmitter release in the nervous system. During early development and adulthood, SNAP-25 appears to have differential influences on short- and long-term synaptic plasticity. The involvement of SNAP-25 in these processes may be different at hippocampal and neocortical synapses because of the presence of two different splice variants, which are developmentally regulated. We show here that the isoform SNAP-25a, which is expressed first developmentally in rodent brain, contributes to developmental regulation of the expression of both long-term depression (LTD) and long-term potentiation (LTP) at Schaffer collateral-CA1 synapses in the hippocampus. In one month old mice lacking the developmentally later expressed isoform SNAP-25b, Schaffer collateral-CA1 synapses showed faster release kinetics, decreased LTP and enhanced LTD. By four months of age, SNAP-25b-deficient mice appeared to have compensated for the lack of the adult SNAP-25b isoform, now exhibiting larger LTP and no differences in LTD compared to wild type mice. Interestingly, learning a hippocampus-dependent task reversed the reductions in LTP, but not LTD, seen at one month of age. In four month old adult mice, learning prevented the compensatory up-regulation of LTD that we observed prior to training. These findings support the hypothesis that SNAP-25b promotes stronger LTP and weakens LTD at Schaffer collateral-CA1 synapses in young mice, and suggest that compensatory mechanisms can reverse alterations in synaptic plasticity associated with a lack of SNAP-25b, once mice reach adulthood.

Indexed as

LearningLong-Term PotentiationAnimalsCA1 Region, HippocampalFemaleMaleMiceMice, KnockoutProtein IsoformsSynapsesSynaptosomal-Associated Protein 25Protein IsoformsSnap25 protein, mouseSynaptosomal-Associated Protein 25cognitionlearning and memorylong-term depressionlong-term potentiationSchaffer collateral-CA1 synapsesSNARE proteins

Identifiers

PMID32093363
PMCPMC7073020
OpenAlexW3007651590

What OpenQuestion holds

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LicenceCC BY
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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.