Hypoxia conditioned adipose-derived stem cell-derived extracellular vesicle therapy improves cardiac function in a rat model of ischemic cardiomyopathy.
Kumagai K., Kawamura T., Torigata K., Harada A., Kishimoto Y., Miyagawa S.
Randomized Controlled Trial on Cardiovascular Disease, Chronic Inflammation, published in Regen Ther (2026) — summary generated from the PubMed abstract.
Several human studies show positive signals, while research methods and sample sizes continue to develop.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Randomized Controlled Trial
- Journal
- Regen Ther (2026)
- Country
- Netherlands
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 41948478
- PMCID
- PMC13051720
- DOI
- 10.1016/j.reth.2026.101105
Abstract (original English)
Extracellular vesicles (EVs) are potential cell-free therapies for cardiac regeneration. Although adipose-derived stem cells (ADSCs) are easily obtained using minimally invasive procedures, therapeutic effects of hypoxically conditioned ADSC-derived EVs on the heart remain unknown. We aimed to verify whether hypoxic preconditioning enhances the therapeutic efficacy of ADSC-derived EVs. Lewis female rats were used to isolate ADSCs and establish an ICM rat model. ADSCs were cultured in a 48-h exosome-free medium under 5% or 20% O 2 , and EVs were recovered using polyethylene glycol and ultracentrifugation. An MI model was created by ligating the left anterior descending artery via mini thoracotomy; EF<45% was confirmed 2 weeks later. Rats were randomly assigned to three groups (PBS, normoxic EV, and hypoxic EV groups), each undergoing mini thoracotomy and myocardial injection. Echocardiography was performed at 2- and 4-weeks post-administration to evaluate cardiac function, and histological analysis of fibrosis and angiogenesis was performed at 4 weeks. We performed miRNA sequencing on both EVs and RNA sequencing on the myocardium 2 days after administration. Functional analysis of EV microRNAs suggested that hypoxia increased levels of miRNAs involved in suppressing fibrosis. Echocardiography at 2 and 4 weeks post-EV administration showed greater improvement in cardiac function
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
Evidence level
Several human studies show positive signals, while research methods and sample sizes continue to develop.
How we grade evidenceBrowse all related research
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