Evidence map›Paper›PMID 37644784›Full record

ArticleJournal of cellular and molecular medicine2023

Avicularin alleviates acute liver failure by regulation of the TLR4/MyD88/NF-κB and Nrf2/HO-1/GPX4 pathways to reduce inflammation and ferroptosis.

Pei Shi, Wentao Zhu, Jiwei Fu, An Liang, Ting Zheng, Zhilong Wen, Xincheng Wu, Yuchen Peng, Songsong Yuan, Xiaoping Wu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  8. Luteolin modulates liver macrophage subtype polarization and play protective role in sepsis induced acute hepatic injury.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
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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 1 institution in 1 country.

Pei ShiDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.ORCID 0009-0005-8677-9012
Wentao ZhuDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Jiwei FuDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.
An LiangDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Ting ZhengDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Zhilong WenDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Xincheng WuDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Yuchen PengDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Songsong YuanDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.ORCID 0009-0001-1953-1624
Xiaoping WuDepartment of Infectious Diseases, The First Affiliated Hospital of Nanchang University, Nanchang, China.ORCID 0000-0003-2747-3185
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute liver failure (ALF) is an inflammation-mediated hepatocyte death process associated with ferroptosis. Avicularin (AL), a Chinese herbal medicine, exerts anti-inflammatory and antioxidative effects. However, the protective effect of AL and the mechanism on ALF have not been reported. Our in vivo results suggest that AL significantly alleviated lipopolysaccharide (LPS)/D-galactosamine (D-GalN)-induced hepatic pathological injury, liver enzymes, inflammatory cytokines, reactive oxygen species and iron levels and increased the antioxidant enzyme activities (malondialdehyde and glutathione). Our further in vitro experiments demonstrated that AL suppressed inflammatory response in LPS-stimulated RAW 264.7 cells via blocking the toll-like receptor 4 (TLR4)/myeloid differentiation protein-88 (MyD88)/nuclear factor kappa B (NF-κB) pathway. Moreover, AL attenuated ferroptosis in D-GalN-induced HepG2 cells by activating the nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase 1 (HO-1)/glutathione peroxidase 4 (GPX4) pathway. Therefore, AL can alleviate inflammatory response and ferroptosis in LPS/D-GalN-induced ALF, and its protective effects are associated with blocking TLR4/MyD88/NF-κB pathway and activating Nrf2/HO-1/GPX4 pathway. Moreover, AL is a promising therapeutic option for ALF and should be clinically explored.

Indexed as

FerroptosisLiver Failure, AcuteAntioxidantsFlavonoidsHeme Oxygenase-1HumansInflammationLipopolysaccharidesLiverMyeloid Differentiation Factor 88NF-E2-Related Factor 2NF-kappa BToll-Like Receptor 4AntioxidantsavicularinFlavonoidsHeme Oxygenase-1LipopolysaccharidesMyeloid Differentiation Factor 88NF-E2-Related Factor 2NF-kappa BTLR4 protein, humanToll-Like Receptor 4acute liver failureavicularinferroptosisinflammationNrf2/HO-1/GPX4TLR4/MyD88/NF-κB

Identifiers

PMID37644784
PMCPMC10623517
OpenAlexW4386272095

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.