Evidence map›Paper›PMID 35460012›Full record

ArticleInflammation2022

Berberine Improves TNF-α-Induced Hepatic Insulin Resistance by Targeting MEKK1/MEK Pathway.

Yaru Li, Xueqin Chen, Yulu Chen, Dongsheng Yu, Ran Jiang, Xinhui Kou, Liang Sheng, Yang Liu, Yu Song

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.0field-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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  14. Preparation, characterization, and protective effects ofFrontiers in cellular and infection microbiology · 2024
    Article
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  17. Review
  18. Current Strategies and Potential Prospects for Nanoparticle-Mediated Treatment of Diabetic Nephropathy.Diabetes, metabolic syndrome and obesity : targets and therapy · 2022
    Review
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

9 authors at 6 institutions in 1 country.

Yaru LiSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Xueqin ChenDepartment of Pharmacology, School of Basic Medical Science, Nanjing Medical University, Nanjing, 211166, Jiangsu, China.
Yulu ChenSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Dongsheng YuDepartment of Traditional Chinese Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China.
Ran JiangSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China.
Xinhui KouDepartment of Pharmacy, Shenzhen Traditional Chinese Medicine Hospital, The Fourth Clinical Medical College of Guangzhou University of Chinese Medicine, Shenzhen, 518033, Guangdong, China. xkou13@fudan.edu.cn.ORCID http://orcid.org/0000-0002-7662-6689
Liang ShengDepartment of Pharmacology, School of Basic Medical Science, Nanjing Medical University, Nanjing, 211166, Jiangsu, China. lgsheng@njmu.edu.cn.
Yang LiuSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, Henan, China. liuyang8016@126.com.
Yu SongSchool of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, Henan, China. songyugzyx@163.com.
Xinxiang Medical University · CNNanjing Medical University · CNFirst Affiliated Hospital of Zhengzhou University · CNGuangzhou University of Chinese Medicine · CNYangzhou University · CNZhengzhou University · CN

Funding

Basic Research Project of Shenzhen Science and Technology Innovation Committee JCYJ20180302173605034the National Nature Science Foundation of China 81900468the Natural Science Foundation of Henan Province 202300410325The Open Research Project of Psychoneurology Cluster of Xinxiang Medical College 2016PN-KFKT-05
6 · The paper itself

Abstract

Berberine (BBR), a natural isoquinoline alkaloid exhibiting insulin sensitizing activity, has been applicated in the treatment of diabetes. However, until now, the exact target of BBR has not been well investigated. Here, primary hepatocytes pre-treated with TNF-α were used to evaluate the role of BBR on hepatic insulin sensitivity. Western blot and immunoprecipitation were used to investigate the effect of BBR on the crosstalk between TNF-α pathway and insulin signaling pathway. Molecular docking was used to verify the interactions between BBR and its potential targets. BBR inhibits the MEKK1 and MEK1/2, and thus suppresses the activation of their downstream ERK1/2. It attenuates the ERK1/2-induced serine phosphorylation of IRS-1 and thus enhances IRS-1 tyrosine phosphorylation and Akt activation. By molecular docking, BBR is proved to efficiently bind MEK1/2. MEKK1 is also considered as BBR target for its similarity in primary structure with MEK1/2. In conclusion, BBR ameliorates TNF-α-induced hepatic insulin resistance by targeting MEKK1 and MEK1/2.

Indexed as

BerberineInsulin ResistanceHumansInsulinIsoquinolinesMAP Kinase Signaling SystemMitogen-Activated Protein Kinase KinasesMolecular Docking SimulationPhosphorylationProto-Oncogene Proteins c-aktSerineTumor Necrosis Factor-alphaTyrosineBerberineInsulinIsoquinolinesMitogen-Activated Protein Kinase KinasesProto-Oncogene Proteins c-aktSerineTumor Necrosis Factor-alphaTyrosineBerberineERK1/2Insulin resistanceMEK1/2MEKK1

Identifiers

PMID35460012
OpenAlexW4224218807

What OpenQuestion holds

Textmetadata
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.