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Updated: Feb 15, 2026

Author Spotlight: Assessing Ischemic Stroke Damage Through Middle Cerebral Artery Occlusion Model
Published on: August 11, 2023
Progression of vasogenic edema induced by activated microglia under permanent middle cerebral artery occlusion
Miki Tanaka1, Yasuhiro Ishihara2, Shodo Mizuno3
1Laboratory of Molecular Brain Science, Graduate School of Integrated Arts and Sciences, Hiroshima University, Hiroshima, 739-8521, Japan; Laboratory for Pharmacotherapy and Experimental Neurology, Kagawa School of Pharmaceutical Sciences, Tokushima Bunri University, Kagawa, 769-2193, Japan.
Abstract:
Brain edema is a severe complication that accompanies ischemic stroke. Increasing evidence shows that inflammatory cytokines impair tight junctions of the blood-brain barrier, suggesting the involvement of microglia in brain edema. In this study, we examined the role of microglia in the progression of ischemic brain edema using mice with permanent middle cerebral artery occlusion. The intensity of T2-weighted imaging (T2WI) in the cerebral cortex and the striatum was elevated 3 h after occlusion and spread to peripheral regions of the ischemic hemisphere. Merged images of 2,3,5-triphenyl tetrazolium chloride staining and T2WI revealed the exact vasogenic edema region, which spread from the ischemic core to outside the ischemic region. Microglia were strongly activated in the ischemic region 3 h after occlusion and, notably, activated microglia were observed in the non-ischemic region 24 h after occlusion. Pretreatment with minocycline, an inhibitor of microglial activation clearly suppressed not only vasogenic edema but also infarct formation. We demonstrated in this study that vasogenic edema spreads from the ischemic core to the peripheral region, which can be elicited, at least in part, by microglial activation induced by ischemia.
Insights
Microglia activation contributes to brain edema following ischemic stroke. Inhibiting microglia with minocycline reduced both edema and infarct size, highlighting microglia
Area of Science:
- Neuroscience
- Pathology
- Immunology
Background:
- Brain edema is a critical complication of ischemic stroke.
- Inflammatory cytokines and microglia are implicated in blood-brain barrier dysfunction during stroke.
Purpose of the Study:
- To investigate the role of microglia in the development and spread of ischemic brain edema.
- To assess the therapeutic potential of inhibiting microglial activation in stroke models.
Main Methods:
- Permanent middle cerebral artery occlusion model in mice.
- T2-weighted imaging (T2WI) and 2,3,5-triphenyl tetrazolium chloride staining for edema assessment.
- Evaluation of microglial activation and infarct volume.
- Administration of minocycline, a microglial activation inhibitor.
Main Results:
- Vasogenic edema expanded from the ischemic core to peripheral regions within 24 hours.
- Microglial activation was observed in both ischemic and non-ischemic areas post-occlusion.
- Minocycline treatment significantly reduced vasogenic edema and infarct size.
Conclusions:
- Microglial activation plays a significant role in the progression of ischemic brain edema.
- Targeting microglial activation may be a viable therapeutic strategy for stroke treatment.
- Edema spread is influenced by microglial responses originating from the ischemic core.
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