Evidence map›Paper›PMID 24553731›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Pharmacological rescue of cortical synaptic and network potentiation in a mouse model for fragile X syndrome.

Tao Chen, Jing-Shan Lu, Qian Song, Ming-Gang Liu, Kohei Koga, Giannina Descalzi, Yun-Qing Li, Min Zhuo

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
  2. Enhanced long-term potentiation in the anterior cingulate cortex of tree shrew.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  3. Cage effects on synaptic plasticity and its modulation in a mouse model of fragile X syndrome.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. TestingFrontiers in molecular neuroscience · 2021
    Article
  11. Review
  12. Cortical plasticity as synaptic mechanism for chronic pain.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Loss of Synaptic Tagging in the Anterior Cingulate Cortex after Tail Amputation in Adult Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  17. Article
  18. Article
  19. Of Men and Mice: Modeling the Fragile X Syndrome.Frontiers in molecular neuroscience · 2018
    Article
  20. Selective Phosphorylation of AMPA Receptor Contributes to the Network of Long-Term Potentiation in the Anterior Cingulate Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    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

8 authors at 3 institutions in 2 countries.

Tao Chen1] Center for Neuron and Disease, Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, China [2] Department of Anatomy and KK Leung Brain Research Center, Fourth Military Medical University, Xi'an, China.
Jing-Shan LuCenter for Neuron and Disease, Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, China.
Qian SongCenter for Neuron and Disease, Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, China.
Ming-Gang Liu1] Center for Neuron and Disease, Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, China [2] Department of Physiology, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Kohei Koga1] Center for Neuron and Disease, Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, China [2] Department of Physiology, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Giannina DescalziDepartment of Physiology, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Yun-Qing LiDepartment of Anatomy and KK Leung Brain Research Center, Fourth Military Medical University, Xi'an, China.
Min Zhuo1] Center for Neuron and Disease, Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an, China [2] Department of Physiology, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Xi'an Jiaotong University · CNUniversity of Toronto · CAAir Force Medical University · CN

Funding

Canadian Institutes of Health Research MOP-124807
6 · The paper itself

Abstract

Fragile X syndrome, caused by the mutation of the Fmr1 gene, is characterized by deficits of attention and learning ability. In the hippocampus of Fmr1 knockout mice (KO), long-term depression is enhanced whereas long-term potentiation (LTP) including late-phase LTP (L-LTP) is reduced or unaffected. Here we examined L-LTP in the anterior cingulate cortex (ACC) in Fmr1 KO mice by using a 64-electrode array recording system. In wild-type mice, theta-burst stimulation induced L-LTP that does not occur in all active electrodes/channels within the cingulate circuit and is typically detected in ∼75% of active channels. Furthermore, L-LTP recruited new responses from previous inactive channels. Both L-LTP and the recruitment of inactive responses were blocked in the ACC slices of Fmr1 KO mice. Bath application of metabotropic glutamate receptor 5 (mGluR5) antagonist or glycogen synthase kinase-3 (GSK3) inhibitors rescued the L-LTP and network recruitment. Our results demonstrate that loss of FMRP will greatly impair L-LTP and recruitment of cortical network in the ACC that can be rescued by pharmacological inhibition of mGluR5 or GSK3. This study is the first report of the network properties of L-LTP in the ACC, and provides basic mechanisms for future treatment of cortex-related cognitive defects in fragile X patients.

Indexed as

Long-Term PotentiationAnimalsDisease Models, AnimalFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeGlycogen Synthase Kinase 3Gyrus CinguliMaleMiceMice, KnockoutNerve NetReceptor, Metabotropic Glutamate 5Fmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Glycogen Synthase Kinase 3Receptor, Metabotropic Glutamate 5

Identifiers

PMID24553731
PMCPMC4059905
OpenAlexW2039348718

What OpenQuestion holds

Textmetadata
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.