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Updated: Aug 29, 2025

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Pre-Chiasmatic, Single Injection of Autologous Blood to Induce Experimental Subarachnoid Hemorrhage in a Rat Model
Published on: June 18, 2021
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Exosomes in subarachnoid hemorrhage: A scoping review
Abhiraj D Bhimani1, Roshini Kalagara1, Susmita Chennareddy1
1Department of Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Summary
Exosomes show promise for treating vasospasm after subarachnoid hemorrhage (SAH). These tiny vesicles, carrying microRNAs (miRNAs), may offer neuroprotection by reducing inflammation and apoptosis, warranting further research.
Area of Science:
- Neuroscience
- Biomedical Engineering
- Regenerative Medicine
Background:
- Subarachnoid hemorrhage (SAH) frequently leads to vasospasm, exacerbating ischemia and brain injury, significantly impacting patient outcomes.
- Current vasospasm treatments offer limited efficacy and unclear clinical benefits.
- Exosomes, particularly their microRNA (miRNA) cargo, are emerging as a potential therapeutic strategy for vasospasm.
Purpose of the Study:
- To conduct a scoping review of existing literature on the role of exosomes in the context of SAH.
- To identify and analyze studies investigating exosomal profiles and therapeutic applications in SAH.
Main Methods:
- A systematic scoping review was performed following PRISMA guidelines.
- Literature searches were conducted in PubMed and Scopus databases.
- Included studies focused on exosomal profiles or therapies for SAH and early brain injury (EBI).
Main Results:
- Seven papers were included, with two analyzing endogenous exosome profiles post-SAH.
- Four studies characterized miRNA-based exosomal therapies for attenuating EBI.
- All therapeutic studies indicated anti-apoptotic and anti-inflammatory effects of miRNA exosomes via specific molecular pathways (BDNF/TrkB/CREB or HDAC3/NF-κB).
Conclusions:
- miRNA-based exosomal treatments show potential neuroprotective benefits for EBI and SAH.
- Further research is recommended to explore the anti-inflammatory and anti-apoptotic roles of exosomal miRNA delivery in SAH.
- Targeting identified common molecular pathways (BDNF/TrkB/CREB or HDAC3/NF-κB) in future SAH exosome therapy is suggested.

