Evidence map›Paper›PMID 42485541›Full record

ArticleJournal of biochemical and molecular toxicology2026

PERK Signaling Pathway Mediates the Hepatoprotective Effects of Naringenin Against Cadmium-Induced Liver Injury in Rats.

Chengxiang Guo, Hao Ling, Mengmeng Gao, Yinan Hu, Jing Zhu, Jicang Wang

Abstract read
In one paragraph

Article in Journal of biochemical and molecular toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Chengxiang GuoCollege of Animal Science and Technology, Henan University of Science and Technology, Luoyang, PR China.ORCID https://orcid.org/0000-0003-1414-9706
Hao LingCollege of Animal Science and Technology, Henan University of Science and Technology, Luoyang, PR China.ORCID https://orcid.org/0009-0001-7299-0352
Mengmeng GaoCollege of Animal Science and Technology, Henan University of Science and Technology, Luoyang, PR China.ORCID https://orcid.org/0009-0009-6113-2078
Yinan HuCollege of Animal Science and Technology, Henan University of Science and Technology, Luoyang, PR China.
Jing ZhuCollege of Animal Science and Technology, Henan University of Science and Technology, Luoyang, PR China.
Jicang WangCollege of Animal Science and Technology, Henan University of Science and Technology, Luoyang, PR China.

Funding

National Nature Science Foundation of China 32273083National Nature Science Foundation of China 32473106
6 · The paper itself

Abstract

Cadmium (Cd), a heavy metal element with extensive industrial applications, exhibits significant toxicological risks in biological systems (Zhu et al. 2019). Naringenin (Nar), a bioactive flavonoid possessing potent antioxidant properties, demonstrates ameliorative effects against Cd toxicity. 24 male SD rats were randomly allocated into four groups: Control group; Cd group; Cd + Nar group; Nar group. Determination of biochemical indicators, antioxidant indicators; reverse transcription quantitative real-time PCR (RT-qPCR) and Western blot were used to detect the expression levels of related mRNA and protein. Cd exposure reduced rat body weight and increased liver-to-body weight ratio, along with elevations in ALT, AST, GSH, and MDA. Conversely, Cd + Nar treatment increased body weight, reduced liver organ coefficient, and decreased these biomarkers. HE staining revealed expanded hepatic sinusoids in the Cd group. RT-qPCR and Western blot showed Cd upregulated GRP78, PERK, and CHOP expression at both mRNA and protein levels, while Cd + Nar treatment attenuated these increases. Cd activates the PERK signaling pathway through ERS and causes liver damage. Nar can reduce liver toxicity. The mechanism may be related to the inhibition of PERK activation by Nar.

Indexed as

CadmiumChemical and Drug Induced Liver InjuryeIF-2 KinaseFlavanonesLiverSignal TransductionAnimalsEndoplasmic Reticulum Chaperone BiPMaleRatsRats, Sprague-DawleyTranscription Factor CHOPCadmiumeIF-2 KinaseEndoplasmic Reticulum Chaperone BiPFlavanonesGRP78 protein, ratnaringeninTranscription Factor CHOPcadmiumendoplasmic reticulum stresslivernaringeninPERK

Identifiers

PMID42485541
PMCPMC13390934

What OpenQuestion holds

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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.