Evidence map›Paper›PMID 41261435›Full record

ArticleJournal of nanobiotechnology2025

Chinese leek-derived extracellular vesicles ameliorate sarcopenia by regulating mitochondrial biogenesis and autophagy via AMPK and maintaining myosin homeostasis.

Weihui Qi, Libin Yang, Yanli Pan, Ke Lv, Lan Zhao, Yujun Zhang, Guoyin Kai, YueLi Sun, Hao Pan, Dong Wang

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. ASIV Attenuates Cisplatin-Induced Proximal Tubular Injury by Enhancing Mitochondrial Biogenesis and Mitophagy Through the ADRA1A/AMPK/FOXO3A Pathway.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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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

10 authors.

Weihui QiDepartment of Orthopaedics, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Tiyuchang Road NO 453, Hangzhou, 310007, China.
Libin YangDepartment of Orthopaedics, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Tiyuchang Road NO 453, Hangzhou, 310007, China.
Yanli PanDepartment of Orthopaedics, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Tiyuchang Road NO 453, Hangzhou, 310007, China.
Ke LvDepartment of Orthopaedics, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Tiyuchang Road NO 453, Hangzhou, 310007, China.
Lan ZhaoDepartment of Orthopaedics, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Tiyuchang Road NO 453, Hangzhou, 310007, China.
Yujun ZhangDepartment of Orthopaedics, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Tiyuchang Road NO 453, Hangzhou, 310007, China.
Guoyin KaiZhejiang Provincial Key TCM Laboratory for Chinese Resource Innovation and Transformation, Hangzhou, 310053, China. kaiguoyin@163.com.
YueLi SunLonghua Hospital, Shanghai University of TCM, Shanghai, 200032, China. Yueli_sun@foxmail.com.
Hao PanDepartment of Orthopaedics, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Tiyuchang Road NO 453, Hangzhou, 310007, China. harper1966@alu.zcmu.edu.cn.
Dong WangDepartment of Orthopaedics, Hangzhou Traditional Chinese Medicine Hospital Affiliated to Zhejiang Chinese Medical University, Tiyuchang Road NO 453, Hangzhou, 310007, China. hz-wdong@alu.zcmu.edu.cn.

Funding

Key Discipline of Traditional Chinese Medicine in Zhejiang Province 2024-XK-57Project of Zhejiang provincial plan for TCM science and technology 2025ZR053The Construction Fund of Key Medical Discipline of Hangzhou 2025HZZD16the Medical and Health Science and Technology Program of Hangzhou ZD20250272The Medical and Health Science and Technology Program of Zhejiang Province 2025KY157The National Natural Science Foundation of China No: 82405429 82505282 and 82575104Zhejiang Provincial Natural Science Foundation of China LQN25H270019
6 · The paper itself

Abstract

Sarcopenia, a prevalent age-related degenerative disorder, poses significant challenges in geriatric care. Chinese leek demonstrates therapeutic potential against sarcopenia progression, with emerging evidence suggesting its extracellular vesicles (EVs) may mediate these effects. Notably, plant-derived EVs have garnered increasing attention due to their low immunogenicity and capacity for cross-kingdom molecular delivery. This study investigates Chinese leek-derived EVs (CL-EVs) as novel regulators of muscle homeostasis through multi-omics approaches. CL-EVs were isolated via differential ultracentrifugation and characterized using nanoparticle tracking analysis, TEM, and proteomic profiling. Using a dexamethasone (DEX)-induced C2C12 myotube atrophy model, we demonstrated CL-EVs' cellular internalization and dose-dependent restoration of myotube diameter. CL-EVs significantly alleviated DEX-induced mitochondrial impairment in C2C12 cells, evidenced by restored ATP production, reduced ROS levels, and stabilized mitochondrial membrane potential (MMP). Multi-omics analysis revealed CL-EVs activate the AMPK/SIRT1/PGC-1α axis, confirmed by Western blotting. Proteomic analysis identified selenium-associated proteins in CL-EVs. Expanding on selenocompounds' known anti-proteolytic effects through Akt modulation, we demonstrate CL-EVs attenuate myotube atrophy through dual mechanisms: inactivation of Akt/FoxO3a/Atrogin-1/MuRF1 proteolytic signaling and activation of mitochondrial biogenesis/mitophagy pathways, collectively improving muscle homeostasis. To investigate gut-muscle axis interactions, 16 S rDNA sequencing and untargeted metabolomic profiling were performed on fecal samples. CL-EVs treatment attenuated DEX-induced gut microbiota dysbiosis and correlated metabolic abnormalities in sarcopenic mice. This study establishes CL-EVs as novel regulators of muscle homeostasis through dual modulation of AMPK/SIRT1/PGC-1α activation and Akt/FoxO3a/Atrogin-1/MuRF1 inhibition. This innovative "multi-target & gut-muscle axis" paradigm provides a groundbreaking strategy for sarcopenia therapeutics.

Indexed as

AMP-Activated Protein KinasesAutophagyExtracellular VesiclesOrganelle BiogenesisSarcopeniaAnimalsCell LineDexamethasoneHomeostasisMiceMitochondriaMuscle Fibers, SkeletalSirtuin 1AMP-Activated Protein KinasesDexamethasoneSirtuin 1AMPKAutophagyChinese leekPlant-derived extracellular vesiclesSarcopenia

Identifiers

PMID41261435
PMCPMC12632053

What OpenQuestion holds

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LicenceCC BY-NC-ND
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 OpenQuestion graph.