Evidence map›Paper›PMID 41957048›Full record

ArticleNPJ science of food2026

Cinnamaldehyde mitigates MASLD through SIRT1/FOXO1-induced autophagy and synergistic gut microbiota modulation.

Xiaoran Wang, Yagang Song, Wenyu Zhao, Yuting Liu, Yiping Fu, Yu Zhang, Quanyou Zhao, Mingsan Miao, Wenxia Zhao, Xianbo Wang and 1 more

Abstract read
In one paragraph

Article in NPJ science of food, 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. The Role ofInternational journal of molecular sciences · 2026
    Review
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

11 authors.

Xiaoran WangDepartment of Digestive Diseases, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China.
Yagang SongAcademy of Chinese Medicine Sciences, Henan University of Chinese Medicine, Zhengzhou, China.
Wenyu ZhaoSchool of Rehabilitation Sciences, Henan University of Chinese Medicine, Zhengzhou, China.
Yuting LiuPharmacy College, Henan University of Chinese Medicine, Zhengzhou, China.
Yiping FuAcademy of Chinese Medicine Sciences, Henan University of Chinese Medicine, Zhengzhou, China.
Yu ZhangAcademy of Chinese Medicine Sciences, Henan University of Chinese Medicine, Zhengzhou, China.
Quanyou ZhaoPharmacy College, Henan University of Chinese Medicine, Zhengzhou, China.
Mingsan MiaoAcademy of Chinese Medicine Sciences, Henan University of Chinese Medicine, Zhengzhou, China.
Wenxia ZhaoDepartment of Digestive Diseases, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China.
Xianbo WangCenter for Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China. wwwzp2020@163.com.
Zhanzhan LiAcademy of Chinese Medicine Sciences, Henan University of Chinese Medicine, Zhengzhou, China. wind_lz@hactcm.edu.cn.

Funding

Associates Fund of Henan Province science and technology research and development program 232301420077Central Plains Science and Technology Innovation Young Top Talent Project NA (2024)China Postdoctoral Science Foundation 2023TQ0109, GZB20230196Henan Science Fund for Excellent Young Scholars 242300421090National Administration of Traditional Chinese Medicine Key Discipline Construction Project of High-Level TCM ZYYZDXK-2023005National Natural Science Foundation of China 82304831Young Talent Support Program of Henan Association for Science and Technology 2025HYTP092
6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a global health burden with limited therapeutic options. Cinnamomum cassia, a medicinal-food homologous plant, contains principal bioactive cinnamaldehyde (CA), whose anti-MASLD mechanisms require clarification. ‌This study employed both a high-fat diet (HFD)-induced MASLD model and a free fatty acid (FFA)-stimulated cell model. CA administration attenuated intracellular lipid accumulation in vitro and ameliorated both hepatic steatosis and systemic hyperlipidemia in vivo, while inhibiting hepatic lipid peroxidation. Mechanistically, integrated RNA-seq, network pharmacology, siRNA, immunofluorescence, and transmission electron microscopy analyses identified the SIRT1/FOXO1-autophagy axis as CA's key regulatory pathway. Gut microbiome profiling revealed CA's capacity to ameliorate HFD-induced dysbiosis, particularly enriching Lachnospiraceae_NK4A136. Fecal microbiota transplantation (FMT) and Spearman correlations link serum lipids and hepatic injury factors to gut microbiota, indicating partially microbiota-mediated metabolic modulation by CA. Collectively, CA ameliorates MASLD through coordinated autophagy enhancement and microbial homeostasis restoration, holding promise as a functional food ingredient for ‌metabolic liver disease prevention.

Identifiers

PMID41957048
PMCPMC13249847

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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.