Evidence map›Paper›PMID 42227370›Full record

ArticleEndocrine, metabolic & immune disorders drug targets2026

Investigation of the Mechanism of Action of Liu Miao San in the Treatment of Lipid Metabolism Disorders on the basis of Network Analysis and Dynamic Ultrasound.

Yu-Jia Xu, Hua Hou, Lin Liu, Fang-Jie Bi

Abstract read
In one paragraph

Article in Endocrine, metabolic & immune disorders drug targets, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Yu-Jia XuDepartment of Echocardiography, Zibo Central Hospital, No. 54 Zhangdian District - Communist Youth League West Road, Zibo, 255000, Shandong Province, People's Republic of China.
Hua HouDepartment of Heart Center, Zibo Central Hospital, No. 54 Zhangdian District - Communist Youth League West Road, Zibo, 255000, Shandong Province, People's Republic of China.
Lin LiuDepartment of Heart Center, Zibo Central Hospital, No. 54 Zhangdian District - Communist Youth League West Road, Zibo, 255000, Shandong Province, People's Republic of China.
Fang-Jie BiDepartment of Heart Center, Zibo Central Hospital, No. 54 Zhangdian District - Communist Youth League West Road, Zibo, 255000, Shandong Province, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLipid metabolism disorders are a critical global health issue. Liu Miao San (LMS), a traditional Chinese medicine (TCM) formula, has demonstrated clinical efficacy against these disorders; however, its underlying mechanism remains unclear.

methodsNetwork analysis was performed to predict LMS targets using the TCMSP and ETCM databases, followed by protein-protein interaction (PPI) network construction and GO/KEGG enrichment analyses. These predictions were validated

resultsNetwork analysis identified SREBP1 and PPARγ as core targets. DISCUSSION: LMS ameliorates lipid metabolism disorders through a dual regulatory mechanism: suppressing SREBP1 (reducing fatty acid and cholesterol synthesis) and activating PPARγ (promoting cholesterol efflux and exerting anti-inflammatory effects). This multitarget action addresses both hepatic and systemic lipid dysregulation.

conclusionLMS exerts therapeutic effects via SREBP1/PPARγ modulation, supporting its clinical application in TCM and providing a methodological framework for mechanistic studies of complex herbal formulations.

Indexed as

Drugs, Chinese HerbalLipid MetabolismLipid Metabolism DisordersLiverAnimalsDiet, High-FatHep G2 CellsHumansMalePPAR gammaProtein Interaction MapsRatsRats, Sprague-DawleySterol Regulatory Element Binding Protein 1UltrasonographyDrugs, Chinese HerbalPPAR gammaSterol Regulatory Element Binding Protein 1fatty liverherbal formulationsLipid metabolism disordersLiu Miao Sannetwork analysisultrasound

Identifiers

PMID42227370
PMCPMC13670187

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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.