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Measuring Post-Stroke Cerebral Edema, Infarct Zone and Blood-Brain Barrier Breakdown in a Single Set of Rodent Brain Samples
Published on: October 23, 2020
Methylene Blue Ameliorates Ischemia/Reperfusion-Induced Cerebral Edema: An MRI and Transmission Electron Microscope
Qing Fang1,2,3, Xu Yan1,2,3, Shaowu Li1,2,3
1Beijing Key Laboratory of Central Nervous System Injury, Beijing Neurosurgical Institute, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100050, China.
Abstract:
The neuroprotective effect of methylene blue (MB) has been identified against various brain disorders, including ischemic stroke. In the present study, we evaluated the effects of MB on postischemic brain edema using magnetic resonance imaging (MRI) and transmission electron microscopy (TEM). Adult male rats were subjected to transient focal cerebral ischemia induced by 1 h middle cerebral artery occlusion (MCAO), followed by reperfusion. MB was infused intravenously immediately after reperfusion (3 mg/kg) and again at 3 h post-occlusion (1.5 mg/kg). Normal saline was administered as vehicle control. Sequential MRIs, including apparent diffusion coefficient (ADC) and T2-weighted imaging (T2WI), were obtained at 0.5, 2.5, and 48 h after the onset of stroke. Separated groups of animals were sacrificed at 2.5 and 48 h after stroke for ultrastructural analysis by TEM. In addition, final lesion volumes were analyzed by triphenyltetrazolium chloride (TTC) staining at 48 h after stroke. Ischemic stroke induced ADC lesion volume at 0.5 h during MCAOs that were temporally recovered at 1.5 h after reperfusion. No significant difference in ADC-defined lesion was observed between vehicle and MB treatment groups. At 48 h after stroke, MB significantly reduced ADC lesion and T2WI lesion volume and attenuated cerebral swelling. Consistently, MB treatment significantly decreased TTC-defined lesion volume at 48 h after stroke. TEM revealed remarkable swollen astrocytes, astrocytic perivascular end-feet, and concurrent shrunken neurons in the penumbra at 2.5 and 48 h after MCAO. MB treatment attenuated astrocyte swelling, the perivascular astrocytic foot process, and endothelium and also alleviated neuron degeneration. This study demonstrated that MB could decrease postischemic brain edema and provided additional evidence that future clinical investigation of MB for the treatment of ischemic stroke is warrented.
Insights
Methylene blue (MB) significantly reduced brain swelling and lesion volume in rats after ischemic stroke. This neuroprotective agent warrants further clinical investigation for stroke treatment.
Area of Science:
- Neuroscience
- Pharmacology
- Medical Imaging
Background:
- Methylene blue (MB) exhibits neuroprotective properties relevant to brain disorders like ischemic stroke.
- Postischemic brain edema is a critical complication following stroke, impacting patient outcomes.
Purpose of the Study:
- To investigate the efficacy of methylene blue (MB) in mitigating postischemic brain edema.
- To evaluate the effects of MB on brain lesion volume and ultrastructural changes after focal cerebral ischemia.
Main Methods:
- Adult male rats underwent transient focal cerebral ischemia induced by middle cerebral artery occlusion (MCAO).
- Methylene blue (MB) was administered intravenously post-reperfusion, with saline as vehicle control.
- Magnetic resonance imaging (MRI) and transmission electron microscopy (TEM) were used to assess edema, lesion volume, and ultrastructure.
Main Results:
- MB treatment significantly reduced apparent diffusion coefficient (ADC) and T2-weighted imaging (T2WI) lesion volumes at 48 hours post-stroke.
- MB attenuated cerebral swelling and decreased triphenyltetrazolium chloride (TTC)-defined lesion volume.
- TEM analysis revealed that MB mitigated astrocyte swelling, perivascular edema, and neuronal degeneration in the ischemic penumbra.
Conclusions:
- Methylene blue (MB) effectively decreases postischemic brain edema and lesion volume in a rat model of focal cerebral ischemia.
- MB demonstrates neuroprotective effects by reducing cellular swelling and degeneration.
- These findings support further clinical trials to explore MB as a potential therapeutic agent for ischemic stroke.
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