Evidence map›Paper›PMID 35406631›Full record

ArticleCells2022

Psoralen Suppresses Lipid Deposition by Alleviating Insulin Resistance and Promoting Autophagy in Oleate-Induced L02 Cells.

Yuhao Wang, Yonglun Wang, Fang Li, Jie Zou, Xiaoqian Li, Mengxia Xu, Daojiang Yu, Yijia Ma, Wei Huang, Xiaodong Sun and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 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
1.4field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Hydrogen gas (HFrontiers in pharmacology · 2025
    Article
  4. Review
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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

11 authors at 5 institutions in 1 country.

Yuhao WangWest China School of Pharmacy, Sichuan University, Chengdu 610041, China.
Yonglun WangWest China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu 610041, China.ORCID 0000-0002-9974-5971
Fang LiDepartment of Hepatopancreatobiliary Surgery, Sichuan Cancer Hospital and Institute, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, China.
Jie ZouWest China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu 610041, China.
Xiaoqian LiWest China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu 610041, China.
Mengxia XuWest China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu 610041, China.
Daojiang YuDepartment of Plastic Surgery, The Second Affiliated Hospital of Chengdu Medical College, China National Nuclear Corporation 416 Hospital, Chengdu 610051, China.
Yijia MaWest China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu 610041, China.
Wei HuangDepartment of Endocrinology, Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
Xiaodong SunWest China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu 610041, China.
Yuanyuan ZhangWest China School of Pharmacy, Sichuan University, Chengdu 610041, China.
West China Medical Center of Sichuan University · CNSichuan University · CNAffiliated Hospital of Southwest Medical University · CNChina National Nuclear Corporation · CNUniversity of Electronic Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) held a high global prevalence in recent decades. Hepatic lipid deposition is the major characteristic of NAFLD. We aim to explore the mechanisms of psoralen on lipid deposition in NAFLD. The effects of psoralen on insulin resistance, lipid deposition, the expression and membrane translocation of glucose transporter type 4 (GLUT4), autophagy, and lipogenesis enzymes were determined on sodium oleate-induced L02 cells. Chloroquine and 3-MA were employed. The AMP-activated protein kinase alpha (AMPKα) was knocked down by siRNA. Psoralen alleviated insulin resistance in sodium oleate-induced L02 hepatocytes by upregulating the expression and membrane translocation of GLUT4. Psoralen inhibited lipid accumulation by decreasing the expression of key lipogenesis enzymes. Psoralen promotes autophagy and the autophagic flux to enhance lipolysis. Psoralen promoted the fusion of the autophagosome with the lysosome. Both chloroquine and 3-MA blocked the effects of psoralen on autophagy and lipid accumulation. The AMPKα deficiency attenuated the effects of psoralen on autophagy and lipid accumulation. Our study demonstrated that as an antioxidant, psoralen attenuates NAFLD by alleviating insulin resistance and promoting autophagy via AMPK, suggesting psoralen to be a promising candidate for NAFLD.

Indexed as

Insulin ResistanceNon-alcoholic Fatty Liver DiseaseAMP-Activated Protein KinasesAutophagyChloroquineFicusinHumansLipid MetabolismOleic AcidAMP-Activated Protein KinasesChloroquineFicusinOleic AcidAMPKautophagynon-alcoholic fatty liver diseasepsoralen

Identifiers

PMID35406631
PMCPMC8997557
OpenAlexW4220825104

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.