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Updated: May 29, 2025

An In Vivo Assessment of Blood-Brain Barrier Disruption in a Rat Model of Ischemic Stroke
Published on: March 11, 2018
Assessment of Blood-Brain Barrier Permeability in a Cerebral Ischemia-Reperfusion Model in Rats; A Pilot Study
P Kozler1, D Marešová, J Pokorný
1Institute of Physiology, First Faculty of Medicine, Charles University, Prague, Czech Republic. jaroslav.pokorny@lf1.cuni.cz.
Abstract:
Animal models are an important tool for studying ischemic mechanisms of stroke. Among them, the middle cerebral artery occlusion (MCAO) model via the intraluminal suture method in rodents is closest to human ischemic stroke. It is a model of transient occlusion followed by reperfusion, thus representing cerebral ischemia-reperfusion model that simulates patients with vascular occlusion and timely recanalization. Although reperfusion is very beneficial for the possibility of preserving brain functions after ischemia, it also brings a great risk in the form of brain edema, which can cause the development of intracranial hypertension, and increasing morbidity and mortality. In this paper, we present the results of our own transient reperfusion model of MCAO in which we tested the permeability of the blood-brain barrier (BBB) using Evans blue (EB), an intravital dye with a high molecular weight (68,500 Da) that prevents its penetration through the intact BBB. A total of 15 animals were used in the experiment and underwent the following procedures: insertion of the MCA occluder; assessment of ischemia by 2,3,5 -Triphenyltetrazolium chloride (TTC) staining; assessment of the BBB permeability using brain EB distribution. The results are presented and discussed. The test of BBB permeability using EB showed that 120 minutes after induction of ischemia, the BBB is open for the entry of large molecules into the brain. We intend to use this finding to time the application of neuroprotective agents via ICA injection in our next stroke model. Keywords: Cerebral ischemia-reperfusion model, Middle cerebral artery occlusion, Blood-brain barrier, 2,3,5 -Triphenyltetrazolium chloride, Evans blue.
Insights
The middle cerebral artery occlusion (MCAO) rodent model simulates human stroke with reperfusion. This study found the blood-brain barrier (BBB) becomes permeable to large molecules 120 minutes after MCAO, impacting stroke treatment strategies.
Area of Science:
- Neuroscience
- Cerebrovascular Research
- Animal Models of Stroke
Background:
- Stroke remains a leading cause of death and disability worldwide.
- Animal models are crucial for understanding stroke pathophysiology and testing therapies.
- The middle cerebral artery occlusion (MCAO) model in rodents closely mimics human ischemic stroke, including reperfusion.
Purpose of the Study:
- To characterize the permeability of the blood-brain barrier (BBB) in a transient rodent MCAO model.
- To determine the optimal timing for neuroprotective agent delivery following ischemic stroke.
Main Methods:
- A transient middle cerebral artery occlusion (MCAO) model was established in rodents.
- Ischemia was assessed using 2,3,5-triphenyltetrazolium chloride (TTC) staining.
- Blood-brain barrier (BBB) permeability was evaluated using Evans blue (EB) dye distribution.
Main Results:
- The study utilized 15 animals for the MCAO model and subsequent assessments.
- Evans blue (EB) dye, a high molecular weight molecule, demonstrated significant brain entry.
- BBB permeability was confirmed 120 minutes after the induction of ischemia, indicating opening to large molecules.
Conclusions:
- The transient MCAO model effectively simulates cerebral ischemia-reperfusion relevant to human stroke.
- The blood-brain barrier (BBB) opens approximately 120 minutes post-MCAO, allowing large molecules to enter the brain.
- This finding is critical for timing the administration of neuroprotective agents via intra-arterial injection in future stroke research.
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