Evidence map›Paper›PMID 38361125›Full record

ArticleMolecular psychiatry2024

Running exercise alleviates hippocampal neuroinflammation and shifts the balance of microglial M1/M2 polarization through adiponectin/AdipoR1 pathway activation in mice exposed to chronic unpredictable stress.

Li Liu, Jing Tang, Xin Liang, Yue Li, Peilin Zhu, Mei Zhou, Lu Qin, Yuhui Deng, Jing Li, Yiying Wang and 7 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
17.6field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

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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

17 authors at 1 institution in 1 country.

Li LiuDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Jing TangDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Xin LiangDepartment of Pathology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Yue LiDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Peilin ZhuDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Mei ZhouDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Lu QinDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Yuhui DengDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Jing LiDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Yiying WangDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Lin JiangLab Teaching & Management Center, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Dujuan HuangDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Yuning ZhouDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Shun WangDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Qian XiaoDepartment of Radioactive Medicine, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Yanmin LuoLaboratory of Stem Cells and Tissue Engineering, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China. luoyanmi2013@163.com.ORCID 0000-0001-5662-8524
Yong TangDepartment of Histology and Embryology, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, People's Republic of China. ytang062@163.com.ORCID 0000-0002-8199-3985
Chongqing Medical University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81871073National Natural Science Foundation of China (National Science Foundation of China) 82001435National Natural Science Foundation of China (National Science Foundation of China) 82001436National Natural Science Foundation of China (National Science Foundation of China) 82171522Natural Science Foundation of Chongqing (Natural Science Foundation of Chongqing Municipality) cstc2021jcyj-msxmX0110
6 · The paper itself

Abstract

Running exercise has been shown to alleviate depressive symptoms. However, the mechanism underlying the antidepressant effects of running exercise is not fully understood. The imbalance of M1/M2 microglia phenotype/polarization and concomitant dysregulation of neuroinflammation play crucial roles in the pathogenesis of depression. Running exercise increases circulating levels of adiponectin which is known to cross the blood‒brain barrier and suppress inflammatory responses. AdipoR1 is an adiponectin receptor that is involved in regulating microglial phenotypes and activation states. However, whether running exercise regulates hippocampal microglial phenotypes and neuroinflammation through adiponectin/AdipoR1 to exert its antidepressant effects remains unclear. In the current study, 4 weeks of running exercise significantly alleviated the depressive-like behaviors of chronic unpredictable stress (CUS)-exposed mice. Moreover, running exercise decreased the microglial numbers and altered microglial morphology in three subregions of the hippocampus to restore the M1/M2 balance; these effects were accompanied by regulation of pro-/anti-inflammatory cytokine production and secretion in CUS-exposed mice. These effects may involve elevation of peripheral tissue (adipose tissue and muscle) and plasma adiponectin levels, and hippocampal AdipoR1 levels as well as activation of the AMPK-NF-κB/STAT3 signaling pathway by running exercise. When an adeno-associated virus was used to knock down hippocampal AdipoR1, mice showed depressive-like behaviors and alterations in microglia and inflammatory factor expression in the hippocampus that were similar to those observed in CUS-exposed mice. Together, these results suggest that running exercise maintains the M1/M2 balance and inhibits neuroinflammation in the hippocampus of CUS-exposed mice. These effects might occur via adiponectin/AdipoR1-mediated activation of the AMPK-NF-κB/STAT3 signaling pathway.

Indexed as

AdiponectinDepressionHippocampusMicrogliaNeuroinflammatory DiseasesPhysical Conditioning, AnimalReceptors, AdiponectinSignal TransductionStress, PsychologicalAnimalsCytokinesDisease Models, AnimalInflammationMaleMiceMice, Inbred C57BLAdiponectinadiponectin receptor 1, mouseCytokinesNF-kappa BReceptors, AdiponectinSTAT3 Transcription Factor

Identifiers

PMID38361125
OpenAlexW4391838362

What OpenQuestion holds

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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.