Evidence map›Paper›PMID 38018587›Full record

ArticleImmunity, inflammation and disease2023

Astragalus polysaccharide ameliorates insulin resistance in HepG2 cells through activating the STAT5/IGF-1 pathway.

Xinxin Yue, Wei Hao, Min Wang, Yang Fu

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Journal of traditional and complementary medicine · 2026
    Article
  2. Article
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  4. Article
  5. Research Progress on Chemical Components ofMolecules (Basel, Switzerland) · 2025
    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

4 authors at 2 institutions in 1 country.

Xinxin YueDepartment of Clinical College, HE University, Shenyang, Liaoning, China.
Wei HaoDepartment of Clinical College, HE University, Shenyang, Liaoning, China.
Min WangDepartment of Clinical College, HE University, Shenyang, Liaoning, China.
Yang FuDepartment of Burn and Plastic Surgery, General Hospital of Northern Theater Command, Shenyang, Liaoning, China.ORCID 0000-0002-2052-2995
He University · CNGeneral Hospital of Shenyang Military Region · CN

Funding

Shenyang Support Plan of Science & Technology Innovation Talent for Youth RC180191
6 · The paper itself

Abstract

backgroundInsulin resistance (IR) is considered as a major factor initiating type 2 diabetes mellitus and can lead to a reduction in glucose uptake that mainly occurs in the liver. Astragalus polysaccharide (APC), extracted from the traditional Chinese medicine, has been recorded to suppress IR. However, the underlying mechanism remains inadequately explored.

methodsIR was induced in HepG2 cells which further underwent APC treatment. Cell viability was determined by cell counting kit-8 assay. Pretreatment with AG490, an inhibitor of signal transducer and activator of transcription 5 (STAT5) signaling, was performed for investigating the influence of STAT5 on APC. Glucose uptake level was reflected by 2-deoxyglucose-6-phosphate content determined through colorimetric assay. Expression levels of insulin-like growth factor 1 (IGF-1), IGF-1 receptor (IGF-1R), phosphorylated-STAT5/STAT5, and p-protein kinase B (AKT)/AKT in the cells were assessed by Western blot. Radioimmunoassay (RIA) was used to detect IGF-1 secretion in the cells.

resultsAPC at doses of 10 and 20 mg increased the viability of HepG2 cells with/without IR induction, and abrogated IR-induced inhibition of glucose intake. Meanwhile, APC (10 mg) offset IR-induced inhibition on the expressions of IGF-1R and IGF-1, the activation of AKT and STAT5, and the secretion of IGF-1 in HepG2 cells. More importantly, the reversal effect of APC on IR-induced alterations in HepG2 cells was counteracted by AG490.

conclusionAPC ameliorates IR in HepG2 cells through activating the STAT5/IGF-1 pathway.

Indexed as

Diabetes Mellitus, Type 2Insulin ResistanceGlucoseHep G2 CellsHumansInsulin-Like Growth Factor IPolysaccharidesProto-Oncogene Proteins c-aktSTAT5 Transcription FactorTyrphostinsalpha-cyano-(3,4-dihydroxy)-N-benzylcinnamideGlucoseInsulin-Like Growth Factor IPolysaccharidesProto-Oncogene Proteins c-aktSTAT5 Transcription FactorTyrphostinsastragalus polysaccharideHepG2 cellsinsulin resistancethe STAT5/IGF-1 pathway

Identifiers

PMID38018587
PMCPMC10664394
OpenAlexW4388961821

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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.