Evidence map›Paper›PMID 42163363›Full record

ArticleChinese medicine2026

Narcissoside attenuates atherosclerosis by suppressing CD36-mediated foam cell formation via upregulation of NR4A1.

Ziyuan Wang, Lamei Zhou, Xiaorong Zhang, Zhiren Yao, Yaping Huang, Lei Wang, Ke Pan, Jian Zhang, Hao Zhi, Zhiqi Yin

Abstract read
In one paragraph

Article in Chinese medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Ziyuan Wang *School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Lamei Zhou *Department of Rheumatology, Wuxi Hospital of Traditional Chinese Medicine, Wuxi, 214000, China.
Xiaorong ZhangSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Zhiren YaoSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Yaping HuangSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Lei WangSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Ke PanSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Jian ZhangAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China. zhangjian@jsatcm.com.
Hao ZhiAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China. 70366432@qq.com.
Zhiqi YinSchool of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 211198, China. cpu-yzq@cpu.edu.cn.

Funding

the China Postdoctoral Science Foundation 2023M733899the Jiangsu Funding Program for Excellent Postdoctoral Talent 2023ZB721the National Natural Science Foundation of China 82304337the Natural Science Foundation of Jiangsu Province Academy of Traditional Medicine 2024YZRKXJJ21Wellcome Trust 202101
6 · The paper itself

Abstract

backgroundThe formation of foam cells (FCs) is the major contributor to the development of atherosclerosis (AS). Gynostemma pentaphyllum is widely used to treat AS and exhibits biological activity against FCs formation. Narcissoside (Nar) is an important component from G. pentaphyllum flavonoids. This study aimed to reveal the beneficial effect and underlying mechanism of Nar on inhibiting the formation of FCs in AS.

methodsThe inhibitory effects of Nar on FCs formation were evaluated using Oil Red O staining and flow cytometry in ox-LDL-stimulated THP-1 and BMDMs. High-fat diet (HFD)-induced ApoE

resultsIn vitro, Nar attenuated FCs formation as evidenced by reduced intracellular lipid levels and ox-LDL uptake rates. In vivo, Nar effectively improved lipid profiles and serum inflammatory factors. Histological analysis showed that Nar reduced the area of the necrotic core and lipid accumulation in the aortic roots. Mechanistically, Nar inhibited CD36 transcription by enhancing the expression and nuclear translocation of NR4A1. Mutation of the NR4A1 binding site within the CD36 promoter abolished the inhibitory effect of Nar. Additionally, silencing NR4A1 eliminated Nar's capacity to suppress ox-LDL uptake and downregulate CD36 expression.

conclusionsNar attenuated AS by inhibiting CD36-mediated FCs formation through upregulating the expression and nuclear translocation of NR4A1, highlighting it as a promising therapeutic candidate for AS.

Indexed as

AtherosclerosisCD36Foam cellNarcissosideNR4A1

Identifiers

PMID42163363
PMCPMC13188464

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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.