Evidence map›Paper›PMID 42554184›Full record

ArticleMediators of inflammation2026

Integrating Network Pharmacology and In Vitro Experiments to Elucidate the Antiatherosclerotic Mechanisms of Qingxin Tongmai Yin.

Yangfan Huang, Zhengshu Xia, Zhiyong Yu, Jiaying Song, Jiaqian Fang, Yaohong Song, Rui Chen

Abstract read
In one paragraph

Article in Mediators of inflammation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Yangfan HuangNanjing University of Chinese Medicine, Nanjing, Jiangsu Province, China, njucm.edu.cn.ORCID https://orcid.org/0009-0008-5447-1883
Zhengshu XiaNanjing University of Chinese Medicine, Nanjing, Jiangsu Province, China, njucm.edu.cn.ORCID https://orcid.org/0009-0003-3111-211X
Zhiyong YuDepartment of Cardiology, Taihe County People's Hospital, Fuyang, Anhui Province, China.ORCID https://orcid.org/0009-0006-3103-9276
Jiaying SongKangda College of Nanjing Medical University, Lianyungang, Jiangsu Province, China, njmu.edu.cn.ORCID https://orcid.org/0009-0006-4062-4178
Jiaqian FangNanjing University of Chinese Medicine, Nanjing, Jiangsu Province, China, njucm.edu.cn.ORCID https://orcid.org/0009-0005-4197-6485
Yaohong SongDepartment of Cardiology, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu Province, China, njucm.edu.cn.ORCID https://orcid.org/0009-0003-6794-3636
Rui ChenDepartment of Cardiology, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu Province, China, njucm.edu.cn.ORCID https://orcid.org/0000-0002-6966-1398

Funding

Nanjing Health Science and Technology Development Special Fund Project for 2024 YKK24171Research Project on Traditional Chinese Medicine Preparations in Medical Institutions of Nanjing City NJCC-ZJ-202415Scientific Research Projects on Traditional Chinese medicine and integrated traditional Chinese and Western medicine in Jiangsu Province CYTF2026038Song Yaohong Nanjing Famous Chinese Medicine Practitioner's Studio 2023-NJSMZYGZS-SYH
6 · The paper itself

Abstract

Qingxin Tongmai Yin (QXTMY), a classic traditional Chinese medicine (TCM) formula widely used for cardiovascular and cerebrovascular diseases, has unclear multitarget mechanisms against atherosclerosis (AS). This study integrated network pharmacology with experimental validation to investigate these mechanisms. Network pharmacology identified 128 bioactive compounds and 135 potential targets of QXTMY, highlighting key anti-AS targets such as TNF, IL6, insulin (INS), IL1B, MMP9, CCL2, and ALB, with the AGE-RAGE signaling pathway as a central mechanism; principal active ingredients included quercetin, kaempferol, luteolin, and cryptotanshinone. In vitro experiments using THP-1-derived macrophages induced with phorbol-12-myristate-13-acetate (PMA) and oxidized low-density lipoprotein (ox-LDL) showed that QXTMY significantly suppressed inflammatory responses, inhibited foam cell formation, and downregulated the AGE-RAGE signaling pathway, as measured by Western blot, ELISA, cholesterol quantification, and Nile Red staining. These findings suggest that QXTMY may exert protective effects against AS, potentially via suppression of the AGE-RAGE-mediated inflammatory axis. However, in vivo validation is still required to support these preliminary conclusions.

Indexed as

AtherosclerosisDrugs, Chinese HerbalNetwork PharmacologyHumansLipoproteins, LDLMacrophagesMedicine, Chinese TraditionalSignal TransductionTHP-1 CellsDrugs, Chinese HerbalLipoproteins, LDLoxidized low density lipoproteinAGE-RAGE signaling pathwayatherosclerosisinflammationnetwork pharmacologyQingxin Tongmai Yin decoction

Identifiers

PMID42554184
PMCPMC13439637

What Socratic 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 Socratic graph.