Evidence map›Paper›PMID 35698613›Full record

ArticlePeerJ2022

Resveratrol ameliorates iron overload induced liver fibrosis in mice by regulating iron homeostasis.

Hua Wang, Chuan Jiang, Yakun Yang, Jinghan Li, Yihan Wang, Chaonan Wang, Yonggang Gao

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  15. Chia seeds and coenzyme QScientific reports · 2023
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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

7 authors at 1 institution in 1 country.

Hua Wang *Hebei University of Chinese Medicine, Department of Preventive Medicine, Shijiazhuang, Hebei, China.
Chuan Jiang *Hebei University of Chinese Medicine, Department of Preventive Medicine, Shijiazhuang, Hebei, China.
Yakun YangHebei University of Chinese Medicine, School of Pharmacy, Shijiazhuang, Hebei, China.
Jinghan LiHebei University of Chinese Medicine, Department of Preventive Medicine, Shijiazhuang, Hebei, China.
Yihan WangHebei University of Chinese Medicine, Collge of Basic Medicine, Shijiazhuang, Hebei, China.
Chaonan WangHebei University of Chinese Medicine, Department of Preventive Medicine, Shijiazhuang, Hebei, China.
Yonggang GaoHebei University of Chinese Medicine, Department of Preventive Medicine, Shijiazhuang, Hebei, China.
Hebei University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study is intended to explore the protective effects of resveratrol (RES) on iron overload-induced liver fibrosis and its mechanism. Iron dextran (50 mg/kg) was injected intraperitoneally in all groups except the control group. Mice in the L-RES, M-RES and H-RES groups were gavaged with RES solution at 25, 50 mg/kg and 100 mg/kg, respectively, 4 h before injection of iron dextran every day; mice in the deferoxamine (DFO) group were injected with DFO intraperitoneally (100 mg/kg); mice in the control group received isovolumetric saline. After seven weeks of RES administration, serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) activities and liver hydroxyproline (Hyp) levels were reduced; the malondialdehyde (MDA) activities decreased and the levels of superoxide dismutase (SOD) and glutathione (GSH) were raised. Hematoxylin and eosin (H&E), Prussian, and Masson staining indicated that RES treatment could improve cell damage and reduce hepatic iron deposition and collagen deposition in iron-overload mice. The expression of Bcl-2 was increased, the expression levels of Bax and caspase-3 were decreased under RES treatment. Moreover, RES reduced the expression of hepcidin, ferritin (Ft), divalent metal transporter-1 (DMT-1), transferrin receptor-2 (TFR-2), and raised the expression of ferroprotein-1 (FPN-1). In conclusion, RES could ameliorate iron overload-induced liver fibrosis, and the potential mechanisms may be related to antioxidant, anti-inflammatory, anti-apoptotic, and more importantly, regulation of iron homeostasis by reducing iron uptake and increasing iron export.

Indexed as

DextransIron OverloadAnimalsHomeostasisIronIron-Dextran ComplexLiver CirrhosisMiceResveratrolDextransIronIron-Dextran ComplexResveratrolAntioxidantIron homeostasisIron overloadLiver fibrosisResveratrol

Identifiers

PMID35698613
PMCPMC9188311
OpenAlexW4285744685

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.