AI Article Synopsis

  • The study aims to determine if intravenous mesenchymal stem cells (MSCs) can aid recovery in a rat model of brainstem infarction after posterior circulation stroke.
  • The experiment involved inducing basilar artery occlusion in rats, followed by MSC infusion one day later, with assessments made through MRI, histology, and behavioral tests.
  • Results showed that MSC treatment significantly reduced ischemic lesion size and improved functional recovery compared to the control group, suggesting potential neuroprotective benefits of MSCs in stroke recovery.

Article Abstract

Objective: Morbidity and mortality in patients with posterior circulation stroke remains an issue despite advances in acute stroke therapies. The intravenous infusion of mesenchymal stem cells (MSCs) elicits therapeutic efficacy in experimental supratentorial stroke models. However, since there are few reliable animal models of ischemia in the posterior circulation, the therapeutic approach with intravenous MSC infusion has not been tested. The objective of this study was to test the hypothesis that intravenously infused MSCs provide functional recovery in a newly developed model of brainstem infarction in rats.

Methods: Basilar artery (BA) occlusion (BAO) was established in rats by selectively ligating 4 points of the proximal BA with 10-0 nylon monofilament suture. The intravenous infusion of MSCs was performed 1 day after BAO induction. MRI and histological examinations were performed to assess ischemic lesion volume, while multiple behavioral tests were performed to evaluate functional recovery.

Results: The MSC-treated group exhibited a greater reduction in ischemic lesion volume, while behavioral testing indicated that the MSC-infused group had greater improvement than the vehicle group 28 days after the MSC infusion. Accumulated infused MSCs were observed in the ischemic brainstem lesion.

Conclusions: Infused MSCs may provide neuroprotection to facilitate functional outcomes and reduce ischemic lesion volume as evaluated in a newly developed rat model of persistent BAO.

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Source
http://dx.doi.org/10.3171/2018.4.JNS173121DOI Listing

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