Evidence map›Paper›PMID 41010360›Full record

ArticleLife (Basel, Switzerland)2025

Therapeutic Potential of Astrocyte-Derived Extracellular Vesicles in Post-Stroke Recovery: Behavioral and MRI-Based Insights from a Rat Model.

Yessica Heras-Romero, Axayácatl Morales-Guadarrama, Luis B Tovar-Y-Romo, Diana Osorio Londoño, Roberto Olayo-González, Ernesto Roldan-Valadez

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Yessica Heras-RomeroPhysics Department, Universidad Autónoma Metropolitana, Iztapalapa, Mexico City 09340, Mexico.ORCID 0000-0002-2990-0622
Axayácatl Morales-GuadarramaElectrical Engineering Department, Universidad Autónoma Metropolitana, Iztapalapa, Mexico City 09340, Mexico.ORCID 0000-0002-4072-2572
Luis B Tovar-Y-RomoDepartment of Molecular Neuropathology, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico.ORCID 0000-0003-2605-1378
Diana Osorio LondoñoElectrical Engineering Department, Universidad Autónoma Metropolitana, Iztapalapa, Mexico City 09340, Mexico.ORCID 0000-0002-1686-7608
Roberto Olayo-GonzálezPhysics Department, Universidad Autónoma Metropolitana, Iztapalapa, Mexico City 09340, Mexico.ORCID 0000-0002-1728-958X
Ernesto Roldan-ValadezDivision of Neurosciences, Instituto Nacional de Rehabilitación 'Luis Guillermo Ibarra Ibarra', Mexico City 14389, Mexico.ORCID 0000-0002-7116-5289

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Astrocyte-derived extracellular vesicles (ADEVs) have emerged as promising neuroprotective agents for ischemic stroke. In this study, we evaluated the therapeutic potential of hypoxia-conditioned ADEVs (HxEVs) administered intracerebroventricularly in a rat model of transient middle cerebral artery occlusion (tMCAO). Serial magnetic resonance imaging (MRI) with diffusion tensor imaging (DTI) was performed at 1, 7, 14, and 21 days post-stroke. HxEV treatment produced a significant reduction in infarct volume from day 1, sustained through day 21, and was accompanied by improvements in motor and sensory recovery. DTI analyses showed progressive normalization of fractional anisotropy (FA) and radial diffusivity (RD), particularly in the corpus callosum and striatum, reflecting microstructural repair. In contrast, mean diffusivity (MD) was less sensitive to these treatment effects. Regional differences in therapeutic response were evident, with earlier and more sustained recovery in the corpus callosum than in other brain regions. Histological findings confirmed greater preservation of dendrites and axons in HxEV-treated animals, supporting the role of these vesicles in accelerating post-stroke neurorepair. Together, these results demonstrate that hypoxia-conditioned ADEVs promote both structural and functional recovery after ischemic stroke. They also highlight the value of DTI-derived biomarkers as non-invasive tools to monitor neurorepair. The identification of region-specific therapeutic effects and the validation of reliable imaging markers provide a strong foundation for future research and development.

Indexed as

astrocyte-derived extracellular vesiclesdiffusion tensor imagingischemic strokeMRI biomarkersneuroregenerationrat model

Identifiers

PMID41010360
PMCPMC12471253

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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.