Evidence map›Paper›PMID 37672892›Full record

ArticleRedox biology2023

Low-dose LPS alleviates early brain injury after SAH by modulating microglial M1/M2 polarization via USP19/FOXO1/IL-10/IL-10R1 signaling.

Weihua Tao, Guibo Zhang, Chengyuan Liu, Lide Jin, Xuehua Li, Shuaifeng Yang

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
10.3field-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

35 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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    Review
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  10. Ubiquitin-specific peptidase-19 links TDP-43 aggregation to ER stress.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  11. Review
  12. Mechanisms ofAnimal nutrition (Zhongguo xu mu shou yi xue hui) · 2026
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  14. Review
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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

6 authors at 3 institutions in 1 country.

Weihua TaoDepartment of Neurosurgery, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, China.
Guibo ZhangDepartment of Neurosurgery, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, China.
Chengyuan LiuDepartment of Neurosurgery, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, China.
Lide JinDepartment of Neurosurgery, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, China.
Xuehua LiCenter for AIDS/STD Control and Prevention, Yunnan Center for Disease Control and Prevention, Kunming, Yunnan, China. Electronic address: 13668702530@163.com.
Shuaifeng YangDepartment of Neurosurgery, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, China. Electronic address: yangshuaifeng7@163.com.
Kunming University of Science and Technology · CNFirst People's Hospital of Yunnan Province · CNYunnan Center for Disease Control And Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLow-dose lipopolysaccharide (LPS) protects against early brain injury (EBI) after subarachnoid hemorrhage (SAH). However, the mechanism underlying the neuroprotective roles of low-dose LPS remain largely undefined.

methodsA SAH mice model was established and the pathological changes of brain were evaluated by wet-dry weight method, HE and Nissl staining, and blood-brain barrier (BBB) permeability assay. Cell apoptosis and inflammation were monitored by TUNEL, flow cytometry and ELISA assays. qRT-PCR, immunofluorescence and Western blot were used to detect the expression of microglial polarization-related or oxidative stress-associated markers. Bioinformatics analysis, luciferase and ChIP assays were employed to detect the direct association between FOXO1 and IL-10 promoter. The ubiquitination of FOXO1 in the in vitro SAH model was detected by co-IP.

resultsLow-dose LPS alleviated SAH-induced neurological dysfunction, brain edema, BBB disruption, damage in the hippocampus, neuronal apoptosis and inflammation via modulating microglial M1/M2 polarization by IL-10/IL-10R1 signaling. Mechanistic studies showed that FOXO1 acted as a transcriptional activator of IL-10. USP19 mediated the deubiquitination of FOXO1 to activate IL-10/IL-10R1 signaling, thereby regulating microglial M1/M2 polarization. Functional experiments revealed that low-dose LPS upregulated USP19 to modulate microglial M1/M2 polarization via FOXO1/IL-10/IL-10R1 signaling in SAH mice.

conclusionLow-dose LPS protected against EBI after SAH by modulating microglial M1/M2 polarization via USP19/FOXO1/IL-10/IL-10R1 signaling.

Indexed as

Brain InjuriesSubarachnoid HemorrhageAnimalsEndopeptidasesInterleukin-10LipopolysaccharidesMiceMicrogliaEndopeptidasesInterleukin-10LipopolysaccharidesUSP19 protein, mouseFOXO1IL-10LipopolysaccharideSubarachnoid hemorrhageUSP19

Identifiers

PMID37672892
PMCPMC10494318
OpenAlexW4386187647

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.