Evidence map›Paper›PMID 40582769›Full record

ArticleJournal of microbiology and biotechnology2025

Schisandrin C Improves Chronic Stress-Induced Dyslipidemia in Mice by Regulating Pyroptosis and Autophagy Levels.

Yuling Liu, Wenjun Lu, Yue Huang, Chaozhi Xu, Wanhua Wu, Zongyi Zhang, Yulin Zhang, Shanqian Li, Guixian Wu, Doudou Wang and 4 more

Abstract read
In one paragraph

Article in Journal of microbiology and biotechnology, 2025. 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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0cells of the map it votes in
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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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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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

14 authors.

Yuling LiuSchool of Public Health, Guilin Medical University, Guilin, P.R. China.
Wenjun LuGeneral Practice Department, Affiliated Hospital of Guilin Medical University, Guilin, P.R. China.
Yue HuangDepartment of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, P.R. China.
Chaozhi XuMedical Information Management, School of Humanities and Management, Guilin Medical University, Guilin, P.R. China.
Wanhua WuSchool of Public Health, Guilin Medical University, Guilin, P.R. China.
Zongyi ZhangCommunicable Disease Control Branch, Qingdao Municipal Center for Disease Control and Prevention, Qingdao, P.R. China.
Yulin ZhangDepartment of Nutrition, Second People's Hospital of Ya'an City, Ya'an City, Sichuan Province, P.R. China.
Shanqian LiDepartment of Clinical Nutrition, Liuzhou Workers' Hospital, Liuzhou Guangxi, P.R. China.
Guixian WuSchool of Public Health, Guilin Medical University, Guilin, P.R. China.
Doudou WangSchool of Public Health, Guilin Medical University, Guilin, P.R. China.
Yao XuSchool of Public Health, Guilin Medical University, Guilin, P.R. China.
Meimei ZhengSchool of Public Health, Guilin Medical University, Guilin, P.R. China.
Hongxian WuDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, P.R. China.
Lina HuSchool of Public Health, Guilin Medical University, Guilin, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic stress emerges as a significant risk factor for metabolic disorders, including hyperlipidemia and fatty liver disease. Schisandrin C (SchC), an essential component of Schisandra chinensis lignans, is known to possess lipid-lowering and liver-protective properties. However, the precise mechanisms underlying its action remain incompletely understood. We hypothesized that SchC exerts a protective effect on chronic stress-induced dyslipidemia in mice by modulating hepatic autophagy and pyroptosis. In this study, a dual model was established for 12 weeks, combining chronic stress with a high-fat diet (HFD). SchC or simvastatin were given respectively starting at week 10. Blood, epididymal white adipose tissue and liver were collected for further analysis. Behavioral tests and lipid levels showed that the dual model construction of HFD and chronic stress used in this study was successful in placing mice in a stressful environment and triggering dyslipidemia. SchC intervention effectively impeded the accumulation of eWAT and reduced the increased lipid levels in mice induced by chronic stress. The expression levels of the pyroptosis marker Caspase-1 and other inflammatory factors NLRP3, IL-1β, and IL-18 were significantly reduced in the liver tissues of chronically stressed mice under SchC treatment. Additionally, SchC significantly reduced expression levels of autophagy-related factors such as Beclin-1, the LC3-B/A ratio, P62, and markers related to the autophagy pathway (PI3K/AKT/mTOR). SchC effectively improves dyslipidemia through various pathways including inhibiting the PI3K/AKT/mTOR pathway, promoting autophagy, reducing pyroptosis. This provides a solid theoretical foundation for the clinical application of SchC in the treatment of dyslipidemia and related diseases.

Indexed as

AutophagyDyslipidemiasLignansPolycyclic CompoundsPyroptosisStress, PhysiologicalAnimalsCyclooctanesDiet, High-FatDisease Models, AnimalLiverMaleMiceMice, Inbred C57BLSchisandraSignal TransductionCyclooctanesLignansPolycyclic CompoundsschizandrinautophagyCaspase-1chronic stressdyslipidemiapyroptosisSchisandrin C

Identifiers

PMID40582769
PMCPMC12256839

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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.