Evidence map›Paper›PMID 39381066›Full record

ArticleMediators of inflammation2024

Aloperine Ameliorates Acetaminophen-Induced Acute Liver Injury through HMGB1/TLR4/NF-

Hui Chen, Shu Wang, Qiuyue Chen, Wen Yu, Hao Nie, Lian Liu, Bing Zheng, Quan Gong

Abstract read
In one paragraph

Article in Mediators of inflammation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Involvement of role of HMGB1-NLRP3 pathway in systemic disorders.Frontiers in cell and developmental biology · 2025
    Review
  11. Article
  12. Andrographolide AlleviatesIranian journal of pharmaceutical research : IJPR
    Article
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

8 authors.

Hui ChenDepartment of Laboratory Medicine The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Shu WangDepartment of Immunology School of Medicine Yangtze University, Jingzhou, China.
Qiuyue ChenHubei College of Chinese Medicine, Jingzhou, China.
Wen YuDepartment of Immunology School of Medicine Yangtze University, Jingzhou, China.
Hao NieDepartment of Immunology School of Medicine Yangtze University, Jingzhou, China.
Lian LiuDepartment of Pharmacology School of Medicine Yangtze University, Jingzhou, China.
Bing ZhengDepartment of Immunology School of Medicine Yangtze University, Jingzhou, China.ORCID https://orcid.org/0000-0003-3443-7297
Quan GongDepartment of Immunology School of Medicine Yangtze University, Jingzhou, China.ORCID https://orcid.org/0000-0003-2576-3365

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Aloperine (ALO), an alkaloid isolated from Materials and Methods: An animal model of acute liver injury was induced by intraperitoneal injection of APAP (150 mg/kg). Prior to APAP injection, ALO (40 mg/kg) was administered daily for 7 consecutive days. Serum alanine aminotransferase, aspartate aminotransferase, and lactate dehydrogenase levels were then measured using an automated chemical analyzer. Histopathological changes were evaluated using hematoxylin and eosin staining. Oxidative stress levels were measured by detecting superoxide dismutase (SOD), glutathione (GSH), and malondialdehyde (MDA). Pro-inflammatory cytokines were detected in serum and liver tissues using ELISA and quantitative real-time polymerase chain reaction (q-PCR). The expression of members of the HMGB1/TLR4/NF- Results: Pretreatment with ALO significantly protected mice from APAP-induced acute liver injury, with decreased MDA content, and significantly increased GSH and SOD activities. Furthermore, ALO pretreatment reduced the release of pro-inflammatory cytokines (IL-1 Conclusion: Taken together, ALO can ameliorate APAP-induced acute liver injury by inhibiting oxidative stress, inflammation by inhibiting the HMGB1/TLR4/NF-

Indexed as

AcetaminophenChemical and Drug Induced Liver InjuryHMGB1 ProteinInflammasomesNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinPiperidinesSignal TransductionToll-Like Receptor 4AnimalsLiverMaleMiceMice, Inbred C57BLOxidative StressQuinolizidinesAcetaminophenaloperineHMGB1 ProteinInflammasomesNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousePiperidinesQuinolizidinesTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID39381066
PMCPMC11461077

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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.