Evidence map›Paper›PMID 26019344›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Role of hippocampal β-adrenergic and glucocorticoid receptors in the novelty-induced enhancement of fear extinction.

Jian-Feng Liu, Chang Yang, Jia-Hui Deng, Wei Yan, Hui-Min Wang, Yi-Xiao Luo, Hai-Shui Shi, Shi-Qiu Meng, Bai-Sheng Chai, Qin Fang and 7 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. A Critical Time Window of Neocortex Modulation for Remote Fear Memory in Rats and Humans.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. The crosstalk between CREB and PER2 mediates the transition between mania- and depression-like behavior.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  4. Review
  5. Article
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  8. Locus coeruleus input-modulated reactivation of dentate gyrus opioid-withdrawal engrams promotes extinction.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
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  17. Review
  18. Role of trace amine-associated receptor 1 in nicotine's behavioral and neurochemical effects.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  19. Transcriptional Regulation Involved in Fear Memory Reconsolidation.Journal of molecular neuroscience : MN · 2018
    Review
  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

17 authors at 7 institutions in 2 countries.

Jian-Feng LiuInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and National Institute on Drug Dependence, Peking University, Beijing 100191, China.
Chang YangInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and.
Jia-Hui DengInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and National Institute on Drug Dependence, Peking University, Beijing 100191, China.
Wei YanInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and National Institute on Drug Dependence, Peking University, Beijing 100191, China.
Hui-Min WangInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and National Institute on Drug Dependence, Peking University, Beijing 100191, China.
Yi-Xiao LuoInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and National Institute on Drug Dependence, Peking University, Beijing 100191, China.
Hai-Shui ShiDepartment of Biochemistry and Molecular Biology, Basic Medical College, Hebei Medical University, Shijiazhuang 050017, China.
Shi-Qiu MengInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and National Institute on Drug Dependence, Peking University, Beijing 100191, China.
Bai-Sheng ChaiAffiliated Hospital and School of Pharmacy, Guiyang Medical University, Guiyang 550004, China.
Qin FangAffiliated Hospital and School of Pharmacy, Guiyang Medical University, Guiyang 550004, China.
Ning ChaiInstitute of Mental Health and Hebei Brain Ageing and Cognitive Neuroscience Laboratory, Hebei Medical University, Shijiazhuang 050031, China, and.
Yan-Xue XueNational Institute on Drug Dependence, Peking University, Beijing 100191, China.
Jia SunAffiliated Hospital and School of Pharmacy, Guiyang Medical University, Guiyang 550004, China.
Chen ChenInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and National Institute on Drug Dependence, Peking University, Beijing 100191, China.
Xue-Yi WangInstitute of Mental Health and Hebei Brain Ageing and Cognitive Neuroscience Laboratory, Hebei Medical University, Shijiazhuang 050031, China, and.
Ji-Shi WangAffiliated Hospital and School of Pharmacy, Guiyang Medical University, Guiyang 550004, China, linlu@bjmu.edu.cn jswang_yg@yahoo.com.
Lin LuInstitute of Mental Health/Peking University Sixth Hospital and Key Laboratory of Mental Health, National Clinical Research Center for Mental Disorders and National Institute on Drug Dependence, Peking University, Beijing 100191, China, Peking-Tsinghua Center for Life Sciences and PKU-IDG/McGovern Institute for Brain Research, Peking University, Beijing 100871, China linlu@bjmu.edu.cn jswang_yg@yahoo.com.
Guiyang Medical University · CNPeking University · CNHebei Medical University · CNNational Clinical Research · USNational Institutes for Food and Drug Control · CNChinese Institute for Brain Research · CNPeking University Sixth Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fear extinction forms a new memory but does not erase the original fear memory. Exposure to novelty facilitates transfer of short-term extinction memory to long-lasting memory. However, the underlying cellular and molecular mechanisms are still unclear. Using a classical contextual fear-conditioning model, we investigated the effect of novelty on long-lasting extinction memory in rats. We found that exposure to a novel environment but not familiar environment 1 h before or after extinction enhanced extinction long-term memory (LTM) and reduced fear reinstatement. However, exploring novelty 6 h before or after extinction had no such effect. Infusion of the β-adrenergic receptor (βAR) inhibitor propranolol and glucocorticoid receptor (GR) inhibitor RU486 into the CA1 area of the dorsal hippocampus before novelty exposure blocked the effect of novelty on extinction memory. Propranolol prevented activation of the hippocampal PKA-CREB pathway, and RU486 prevented activation of the hippocampal extracellular signal-regulated kinase 1/2 (Erk1/2)-CREB pathway induced by novelty exposure. These results indicate that the hippocampal βAR-PKA-CREB and GR-Erk1/2-CREB pathways mediate the extinction-enhancing effect of novelty exposure. Infusion of RU486 or the Erk1/2 inhibitor U0126, but not propranolol or the PKA inhibitor Rp-cAMPS, into the CA1 before extinction disrupted the formation of extinction LTM, suggesting that hippocampal GR and Erk1/2 but not βAR or PKA play critical roles in this process. These results indicate that novelty promotes extinction memory via hippocampal βAR- and GR-dependent pathways, and Erk1/2 may serve as a behavioral tag of extinction.

Indexed as

Adrenergic beta-AntagonistsAnimalsExtinction, PsychologicalFearHippocampusMaleMemoryRatsRats, Sprague-DawleyReceptors, Adrenergic, betaReceptors, GlucocorticoidAdrenergic beta-AntagonistsReceptors, Adrenergic, betaReceptors, Glucocorticoidbehavioral tagextinctionglucocorticoid receptorshippocampusβ-adrenergic receptors

Identifiers

PMID26019344
PMCPMC6605349
OpenAlexW1549027883

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.