Evidence map›Paper›PMID 40151124›Full record

ArticleJournal of traditional Chinese medicine = Chung i tsa chih ying wen pan2025

Network pharmacology approach to unveiling the mechanism of berberine in the amelioration of morphine tolerance.

Han Shuai, Du Zhikang, Wang Zirui, Huang Tianfeng, G E Yali, Shi Jianwen, Gao Ju

Abstract read
In one paragraph

Article in Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

4 citing papers in PubMed.

  1. Berberine alleviates alcoholic liver diseaseactivating intestinal nuclear receptor subfamily 1 group D member 1.Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan · 2026
    Article
  2. Article
  3. 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

7 authors.

Han ShuaiInstitute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225009, China.
Du ZhikangInstitute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225009, China.
Wang ZiruiInstitute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225009, China.
Huang TianfengNorthern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou 225009, China.
G E YaliNorthern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou 225009, China.
Shi JianwenPeking University People's Hospital, Qingdao 266111, China.
Gao JuNorthern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou 225009, China.

Funding

Natural Science Foundation-funded Project: Study on the Mechanism of Mechanical Stress Sensing Element Piezo Type Mechanosensitive Ion Channel Component 2 Interacting with Nuclear Receptor Subfamily 4 Group A Member 2 Mediating Traumatic Brain Injury 82172190
6 · The paper itself

Abstract

objectiveTo investigate the mechanism underlying the effect of the Huanglian decoction (, HLD) on morphine tolerance (MT), using network pharmacology, and to verify these mechanisms

methodsAvailable biological data on each drug in the HLD were retrieved from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform. The target proteins of MT were retrieved from the GeneCards, PharmGkb, Therapeutic Target Database, DrugBank, and Online Mendelian Inheritance in Man databases. Information regarding MT and the drug targets was compared to obtain overlapping elements. This information was imported into the Search Tool for the Retrieval of Interacting Genes/Proteins platform to obtain a protein-protein interaction network diagram. Then, a "component-target" network diagram was constructed using screened drug components and target information,

resultsNetwork pharmacology analysis identified 22 active compounds of HLD and revealed that HLD partially ameliorated MT by modulating inflammatory, apoptosis, and nuclear factor kappa B (NF-κB) signaling pathways. Berberine (BBR), one of the main components of HLD, inhibited the development of MT in mice. BBR reduced cell viability while increasing B-cell lymphoma 2 (Bcl-2) protein expression and decreasing CD86, NF-κB, Bax, and Caspase-3 protein expression in brain vascular 2 (BV2) mcroglia cells treated with morphine. Additionally, BBR contributed to a reduction in pro-inflammatory cytokine release and apoptotic cell number.

conclusionsBBR, a key component of HLD, effectively suppressed microglial activation and neuro-inflammation by regulating the NF-κB and apoptosis signaling pathways, thereby delaying MT. This study offers a novel approach to enhance the clinical analgesic efficacy of morphine.

Indexed as

BerberineDrugs, Chinese HerbalDrug ToleranceMorphineAnimalsApoptosisHumansMaleMiceNetwork PharmacologyNF-kappa BProtein Interaction MapsSignal TransductionBerberineDrugs, Chinese HerbalhuanglianMorphineNF-kappa BberberineHuanglian decoctionmicrogliamorphine tolerancenetwork pharmacologyNF-kappa B

Identifiers

PMID40151124
PMCPMC11955763

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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.