Evidence map›Paper›PMID 36160708›Full record

ArticleOxidative medicine and cellular longevity2022

Exploration of the Protective Mechanism of Naringin in the Acetaminophen-Induced Hepatic Injury by Metabolomics.

Zihan Lin, Guanzhen Wang, Wei Gu, Shengchao Zhao, Ziyi Shen, Wei Liu, Guodong Zheng, Baizhong Chen, Yi Cai, Mingxi Li and 2 more

Abstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

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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

12 authors.

Zihan LinSchool of Life Sciences, Shanghai University, 99 Shangda Road, Shanghai 200444, China.
Guanzhen WangSchool of Life Sciences, Shanghai University, 99 Shangda Road, Shanghai 200444, China.
Wei GuSchool of Life Sciences, Shanghai University, 99 Shangda Road, Shanghai 200444, China.
Shengchao ZhaoSchool of Life Sciences, Shanghai University, 99 Shangda Road, Shanghai 200444, China.
Ziyi ShenSchool of Life Sciences, Shanghai University, 99 Shangda Road, Shanghai 200444, China.
Wei LiuUniversity and College Key Lab of Natural Product Chemistry and Application in Xinjiang, School of Chemistry and Environmental Science, Yili Normal University, Yining 835000, China.
Guodong ZhengGuangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target & Clinical Pharmacology, the NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou 511436, China.ORCID https://orcid.org/0000-0003-3708-1193
Baizhong ChenGuangdong Xinbaotang Biological Technology Co., Ltd., Guangdong, Jiangmen 529000, China.
Yi CaiGuangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target & Clinical Pharmacology, the NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou 511436, China.ORCID https://orcid.org/0000-0003-2296-222X
Mingxi LiResearch Center of Tea and Tea Culture, College of Agronomy, Jiangxi Agricultural University, Nanchang 330045, China.ORCID https://orcid.org/0000-0003-3987-017X
Chunpeng Craig WanResearch Center of Tea and Tea Culture, College of Agronomy, Jiangxi Agricultural University, Nanchang 330045, China.ORCID https://orcid.org/0000-0001-6892-016X
Tingdong YanSchool of Life Sciences, Shanghai University, 99 Shangda Road, Shanghai 200444, China.ORCID https://orcid.org/0000-0002-5193-022X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Naringin is a dihydroflavone which was found in citrus fruits. Previous studies have indicated the antiapoptotic, antioxidative stress, and anti-inflammatory effects of naringin. It can improve many common diseases, including fibrosis or hepatotoxicity, cardiovascular disease, and diabetes. Acetaminophen (APAP) is a frequently used painkiller, and hepatotoxic side effects limit its use. The purpose of the current examination is to find the impact of naringin on APAP-induced hepatic injury. Firstly, we pretreated mice model groups with naringin. Then, the liver injury model was established by injecting intraperitoneally into mice with APAP. After the mice were euthanized, we obtained serum and liver tissue samples from the mice. Finally, these samples were analyzed using a metabolomics approach to find the underlying mechanism of the effects of naringin on APAP-induced liver injury and provide a new treatment strategy for APAP-induced liver injury. Our data indicate that naringin significantly improves APAP-induced liver injury in mice and reduces the expression levels of liver injury markers in a dose-dependent manner. Furthermore, analysis of differential metabolites in mice with liver injury showed that naringin reduced APAP-induced hepatotoxicity due to reversing multiple metabolite expression levels and the rescue of energy, amino acid, and purine metabolism.

Indexed as

Chemical and Drug Induced Liver InjuryChemical and Drug Induced Liver Injury, ChronicAcetaminophenAmino AcidsAnimalsAnti-Inflammatory AgentsFlavanonesLiverMiceMice, Inbred C57BLOxidative StressPurinesAcetaminophenAmino AcidsAnti-Inflammatory AgentsFlavanonesnaringinPurines

Identifiers

PMID36160708
PMCPMC9507767

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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.