Evidence map›Paper›PMID 35388184›Full record

ArticleMolecular psychiatry2022

An entorhinal-visual cortical circuit regulates depression-like behaviors.

Jian Lu, Zhouzhou Zhang, Xinxin Yin, Yingjun Tang, Runan Ji, Han Chen, Yu Guang, Xue Gong, Yong He, Wei Zhou and 6 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.9field-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

36 citing papers in PubMed, 52 citations in OpenAlex.

  1. mGluR5 in ECAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. MgSOFrontiers in nutrition · 2025
    Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 2 countries.

Jian LuNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases & Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.ORCID http://orcid.org/0000-0003-1266-1589
Zhouzhou ZhangIDG/McGovern Institute for Brain Research, School of Medicine, Tsinghua University, 100084, Beijing, China.
Xinxin YinIDG/McGovern Institute for Brain Research, School of Medicine, Tsinghua University, 100084, Beijing, China.
Yingjun TangIDG/McGovern Institute for Brain Research, School of Medicine, Tsinghua University, 100084, Beijing, China.
Runan JiIDG/McGovern Institute for Brain Research, School of Medicine, Tsinghua University, 100084, Beijing, China.
Han ChenIDG/McGovern Institute for Brain Research, School of Medicine, Tsinghua University, 100084, Beijing, China.
Yu GuangDepartment of gynecology, The First Affiliated Hospital of Shenzhen University (The Second People's Hospital of Shenzhen) and Dapeng Maternity & Child Healthcare Hospital, 518028, Shenzhen, China.
Xue GongNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases & Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.
Yong HeNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases & Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.
Wei ZhouNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases & Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.
Haiyang WangNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases & Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.
Ke ChengNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases & Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.
Yue WangNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases & Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.
Xiaowei ChenBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, 400038, Chongqing, China.ORCID http://orcid.org/0000-0003-0906-6666
Peng XieNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases & Department of Neurology, The First Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China. xiepeng@cqmu.edu.cn.ORCID http://orcid.org/0000-0002-0081-6048
Zengcai V GuoIDG/McGovern Institute for Brain Research, School of Medicine, Tsinghua University, 100084, Beijing, China. guozengcai@tsinghua.edu.cn.ORCID http://orcid.org/0000-0002-4140-7961
The Affiliated Yongchuan Hospital of Chongqing Medical University · CNChinese Institute for Brain Research · CNArmy Medical University · CNMcGovern Institute for Brain Research · USShenzhen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major depressive disorder is viewed as a 'circuitopathy'. The hippocampal-entorhinal network plays a pivotal role in regulation of depression, and its main sensory output, the visual cortex, is a promising target for stimulation therapy of depression. However, whether the entorhinal-visual cortical pathway mediates depression and the potential mechanism remains unknown. Here we report a cortical circuit linking entorhinal cortex layer Va neurons to the medial portion of secondary visual cortex (Ent→V2M) that bidirectionally regulates depression-like behaviors in mice. Analyses of brain-wide projections of Ent Va neurons and two-color retrograde tracing indicated that Ent Va→V2M projection neurons represented a unique population of neurons in Ent Va. Immunostaining of c-Fos revealed that activity in Ent Va neurons was decreased in mice under chronic social defeat stress (CSDS). Both chemogenetic inactivation of Ent→V2M projection neurons and optogenetic inactivation of the projection terminals induced social deficiency, anxiety- and despair-related behaviors in healthy mice. Chemogenetic inactivation of Ent→V2M projection neurons also aggravated these depression-like behaviors in CSDS-resilient mice. Optogenetic activation of Ent→V2M projection terminals rapidly ameliorated depression-like phenotypes. Optical recording using fiber photometry indicated that elevated neural activity in Ent→V2M projection terminals promoted antidepressant-like behaviors. Thus, the Ent→V2M circuit plays a crucial role in regulation of depression-like behaviors, and can function as a potential target for treating major depressive disorder.

Indexed as

Major Depressive DisorderVisual CortexAnimalsDepressionEntorhinal CortexMiceMice, Inbred C57BLNeuronsStress, Psychological

Identifiers

PMID35388184
OpenAlexW4224980489

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.