Evidence map›Paper›PMID 41212347›Full record

ArticleLangenbeck's archives of surgery2025

Erianin is a therapeutic candidate for addressing neuroinflammation triggered by intracerebral hemorrhage.

Shi-Wei Li, Hong-Cai Wang, Mao-Song Chen

Abstract read
In one paragraph

Article in Langenbeck's archives of surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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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

3 authors.

Shi-Wei LiDepartment of Neurosurgery, Ningbo Medical Center Lihuili Hospital, No.57 XingNing Road, Ningbo, Zhejiang Province, 315000, China. orx244@yeah.net.
Hong-Cai WangDepartment of Neurosurgery, Ningbo Medical Center Lihuili Hospital, No.57 XingNing Road, Ningbo, Zhejiang Province, 315000, China.
Mao-Song ChenDepartment of Neurosurgery, Ningbo Medical Center Lihuili Hospital, No.57 XingNing Road, Ningbo, Zhejiang Province, 315000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuroinflammation is a common consequence of intracerebral hemorrhage (ICH), leading to neurological impairments. Research indicates that the gut microbiome can influence neuroinflammatory responses. Erianin, is a potential therapeutic agent in the treatment of inflammation. Yet, the specific impact of erianin on ICH-induced inflammation and its interaction with the gut microbiome remain areas of ongoing investigation.

methodsICH mouse model was established and treated with erianin. Neurobehavioral tests, brain water content, immunofluorescence, western blotting, and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining were performed to measure the neurological defects and neuroinflammation and neuron apoptosis. Immunofluorescent staining and western blotting assay were performed to assess the activation states of microglia and inflammation. The quantitative real-time polymerase chain reaction (qRT-PCR), enzyme-linked immunosorbent assay (ELISA), and FITC-dextran assays were utilized to measure the intestinal barrier integrity. The composition of the gut microbiota was analyzed by sequencing the 16 S rRNA extracted from fecal samples.

resultsAdministration of Erianin notably decreased inflammation in the brain and improved neurological function in ICH mice by inhibiting the proinflammatory activation of microglia. Additionally, Erianin bolstered intestinal barrier integrity, evidenced by decreased levels of lipopolysaccharide-binding protein. Furthermore, treatment with Erianin led to observable shifts in the gut microbiota. Notably, the activation of the ERK signaling pathway was found to counteract the neuroprotective effects of Erianin following ICH.

conclusionsErianin is a therapeutic candidate for addressing neuroinflammation triggered by ICH, with its mechanisms of action likely involving the modulation of ERK signaling and the gut microbiome.

Indexed as

Cerebral HemorrhageNeuroinflammatory DiseasesAnimalsDisease Models, AnimalGastrointestinal MicrobiomeMaleMiceMice, Inbred C57BL16S rRNAERK signalingIntracerebral hemorrhageMouse modelQuantitative real-time polymerase chain reaction

Identifiers

PMID41212347
PMCPMC12602632

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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.