Evidence map›Paper›PMID 35761401›Full record

ArticleJournal of neuroinflammation2022

Astrocyte reactivation in medial prefrontal cortex contributes to obesity-promoted depressive-like behaviors.

Gang Yu, Feng Cao, Tingting Hou, Yunsheng Cheng, Benli Jia, Liang Yu, Wanjing Chen, Yanyan Xu, Mingming Chen, Yong Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  8. Astrocytic RARγ mediates hippocampal astrocytosis and neurogenesis deficits in chronic retinoic acid-induced depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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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

10 authors at 2 institutions in 2 countries.

Gang Yu *Department of Gastrointestinal Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Feng Cao *Department of Gastrointestinal Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Tingting Hou *College of Pharmacy, Sanquan College of Xinxiang Medical University, Xinxiang, 453000, China.
Yunsheng ChengDepartment of Gastrointestinal Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Benli JiaDepartment of Gastrointestinal Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Liang YuDepartment of Gastrointestinal Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Wanjing ChenDepartment of Gastrointestinal Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Yanyan XuDepartment of Gastrointestinal Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Mingming ChenChinese Medicine Modernization and Big Data Research Center, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine, Nanjing, 210022, China. mingming.chen@yale.edu.
Yong WangDepartment of Gastrointestinal Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China. wangyong@ahmu.edu.cn.ORCID http://orcid.org/0000-0001-8540-6285
Anhui Medical University · CNNanjing University of Chinese Medicine · CN

Funding

National Natural Science Foundation of China 82101583Open Fund of Medical Physics and Technology of Anhui Provincial Key Laboratory LMPT201908
6 · The paper itself

Abstract

backgroundLittle is known about how the obesogenic environment influences emotional states associated with glial responses and neuronal function. Here, we investigated glial reactivation and neuronal electrophysiological properties in emotion-related brain regions of high-fat diet (HFD) and ob/ob mice under chronic stress.

methodsThe glial reactivation and neuronal activities in emotion-related brain regions were analyzed among normal diet mice (ND), HFD mice, wild-type mice, and ob/ob mice. To further activate or inhibit astrocytes in medial prefrontal cortex (mPFC), we injected astrocytes specific Gq-AAV or Gi-AAV into mPFC and ongoing treated mice with CNO.

resultsThe results showed that obesogenic factors per se had no significant effect on neuronal activities in emotion-related brain regions, or on behavioral performance. However, exposure to a chronic stressor profoundly reduced the frequency of spontaneous inhibitory postsynaptic currents (sIPSCs) and spontaneous excitatory postsynaptic currents (sEPSCs) in the mPFC; depressive-like behaviors were seen, accompanied by significant upregulation of astrocyte reactivation. We identified resilient and susceptible mice among chronic social defeat stress-exposed HFD mice. As expected, astrocyte reactivity was upregulated, while neuronal activity was depressed, in the mPFC of susceptible compared to resilient mice. Furthermore, activating astrocytes resulted in similar levels of neuronal activity and depressive-like behaviors between resilient and susceptible mice. Additionally, inhibiting astrocyte reactivation in the mPFC of HFD mice upregulated neuronal activities and inhibited depressive-like behaviors.

conclusionsThese observations indicate that obesogenic factors increase the risk of depression, and improve our understanding of the pathological relationship between obesity and depression.

Indexed as

AstrocytesPrefrontal CortexAnimalsDepressionMiceMice, Inbred C57BLNeuronsObesityStress, PsychologicalAstrocyteChronic social defeated stressDepressionHigh-fat dietmPFCObesityOb/obStress

Identifiers

PMID35761401
PMCPMC9235218
OpenAlexW4283584292

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.