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Assessment of infarct volume in the mouse brain: correlation of magnetic resonance imaging with morphometry

E Weber1, P R Allegrini, D Sauer

  • 1Experimental Pathology, Ciba Ltd., Basle, Switzerland.

Insights

Researchers studied brain damage in mice after middle cerebral artery occlusion. Magnetic resonance imaging (MRI) and histology showed that the N-methyl-D-aspartate receptor antagonist MK 801 reduced brain atrophy and tissue loss.

Area of Science:

  • Neuroscience
  • Cerebrovascular Research
  • Pharmacology

Background:

  • Focal cerebral ischemia, induced by middle cerebral artery occlusion (MCAO), is a leading cause of brain injury.
  • Understanding the long-term consequences of ischemic stroke and potential neuroprotective strategies is crucial.

Purpose of the Study:

  • To investigate the relationship between early cerebral edema volume and long-term brain atrophy following MCAO in a mouse model.
  • To evaluate the cerebroprotective efficacy of the N-methyl-D-aspartate (NMDA) receptor antagonist MK-801 in this model.

Main Methods:

  • Induction of focal necrotic lesions via left middle cerebral artery occlusion in mice.
  • Quantification of cerebral edema volume using in vivo magnetic resonance imaging (MRI) at two days post-occlusion.
  • Histological examination and morphometric analysis of brain atrophy after 2-3 months of survival.

Main Results:

  • A significant correlation was observed between the volume of cerebral edema measured by MRI and the extent of brain atrophy determined by morphometry.
  • Histological analysis revealed predominantly cortical tissue loss in the affected hemisphere.
  • Treatment with MK-801 demonstrated a significant cerebroprotective effect, reducing the extent of brain damage.

Conclusions:

  • Early-stage cerebral edema volume is a reliable predictor of long-term brain atrophy after ischemic stroke.
  • MK-801 exhibits neuroprotective properties against ischemic brain injury, mitigating tissue loss and atrophy.

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