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Stem Cell Transplantation in an in vitro Simulated Ischemia/Reperfusion Model
Published on: November 5, 2011
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Cell Therapy: A New Technology for Cerebral Circulation Restoration after Ischemia/Reperfusion
1Pavlov Institute of Physiology, Russian Academy of Sciences, St. Petersburg, 199034 Russian Federation.
Acta Naturae
|August 4, 2023
Summary
Delayed transplantation of human mesenchymal stem cells (hMSCs) effectively restores cerebral blood flow and vasculature density after transient ischemic attacks in rats. This cell therapy approach shows promise for improving outcomes following cerebral ischemia.
Area of Science:
- Neuroscience
- Regenerative Medicine
- Vascular Biology
Background:
- Transient cerebral ischemia can lead to impaired cerebral blood flow and microvascular dysfunction.
- Mesenchymal stem cells (MSCs) are being investigated for their therapeutic potential in neurological recovery.
- A 7-9 day cultivation period is necessary for preparing MSCs for transplantation.
Purpose of the Study:
- To evaluate the efficacy of delayed human MSC (hMSC) transplantation in restoring cerebral circulation after transient ischemic/reperfusion (I/R) injury.
- To assess the impact of hMSC therapy on vasculature density, pial artery reactivity, and cortical perfusion in a rat model.
Main Methods:
- Induction of cerebral I/R in rats by carotid artery clamping and induced hypotension.
- Intravital microscopy to assess pial vasculature density and acetylcholine-induced arterial dilation.
- Laser dopplerography to measure sensorimotor cortex perfusion.
- Administration of hMSCs 7 days post-I/R and evaluation at 14 and 21 days.
Main Results:
- Ischemia/reperfusion significantly reduced vasculature density and arterial reactivity, and decreased cortical perfusion.
- hMSC transplantation on day 7 post-I/R led to complete vasculature density recovery by day 14.
- ACh-mediated arterial dilation recovered in smaller vessels (<40 μm) within 21 days.
- Cortical perfusion showed significant improvement in hMSC-treated rats compared to untreated I/R rats.
Conclusions:
- Delayed hMSC administration after transient cerebral ischemia is a viable therapeutic strategy.
- hMSC therapy promotes significant recovery of cerebral microvasculature and perfusion.
- This approach allows sufficient time for cell preparation and demonstrates a beneficial therapeutic response in the pial microvasculature.

