Evidence map›Paper›PMID 29555855›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Autophagy Enhances Memory Erasure through Synaptic Destabilization.

Mohammad Shehata, Kareem Abdou, Kiriko Choko, Mina Matsuo, Hirofumi Nishizono, Kaoru Inokuchi

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% 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, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Epigenetic regulation ofAutophagy · 2024
    Review
  15. Review
  16. Article
  17. Review
  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

6 authors at 3 institutions in 1 country.

Mohammad ShehataDepartment of Biochemistry, Graduate School of Medicine and Pharmaceutical Sciences, inokuchi@med.u-toyama.ac.jp mohammad.shehata@gmail.com.ORCID 0000-0003-1710-3009
Kareem AbdouDepartment of Biochemistry, Graduate School of Medicine and Pharmaceutical Sciences.ORCID 0000-0002-1033-1650
Kiriko ChokoDepartment of Biochemistry, Graduate School of Medicine and Pharmaceutical Sciences.
Mina MatsuoDivision of Animal Experimental Laboratory, Life Science Research Center, University of Toyama, Toyama, 930-0194, Japan.
Hirofumi NishizonoJapan Science and Technology Agency, Core Research for Evolutional Science and Technology, and.
Kaoru InokuchiDepartment of Biochemistry, Graduate School of Medicine and Pharmaceutical Sciences, inokuchi@med.u-toyama.ac.jp mohammad.shehata@gmail.com.ORCID 0000-0002-5393-3133
Japan Science and Technology Agency · JPOkayama University · JPUniversity of Toyama · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is substantial interest in memory reconsolidation as a target for the treatment of anxiety disorders, such as post-traumatic stress disorder. However, its applicability is restricted by reconsolidation-resistant boundary conditions that constrain the initial memory destabilization. In this study, we investigated whether the induction of synaptic protein degradation through autophagy modulation, a major protein degradation pathway, can enhance memory destabilization upon retrieval and whether it can be used to overcome these conditions. Here, using male mice in an auditory fear reconsolidation model, we showed that autophagy contributes to memory destabilization and its induction can be used to enhance erasure of a reconsolidation-resistant auditory fear memory that depended on AMPAR endocytosis. Using male mice in a contextual fear reconsolidation model, autophagy induction in the amygdala or in the hippocampus enhanced fear or contextual memory destabilization, respectively. The latter correlated with AMPAR degradation in the spines of the contextual memory-ensemble cells. Using male rats in an

Indexed as

AutophagyMemorySynaptic TransmissionAmygdalaAnimalsEndocytosisHippocampusMaleMiceMice, Inbred C57BLProteolysisRatsRats, WistarReceptors, AMPAReceptors, N-Methyl-D-AspartateReceptors, AMPAReceptors, N-Methyl-D-AspartateAMPA receptorslong-term potentiationNMDA receptorspost-traumatic stress disorderprotein degradationreconsolidation

Identifiers

PMID29555855
PMCPMC6705918
OpenAlexW2783503227

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.