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E-129 Selective middle cerebral artery occlusion in the rabbit: technique and characterization with pathologic findings and multimodal MRI
  1. R Jahan1,
  2. P Villablanca2,
  3. R Harris3,
  4. S Duarte-Vogel4,
  5. C Williams5,
  6. H Vinters5,
  7. N Rao6,
  8. D Enzmann3,
  9. B Ellingson3
  1. 1Division of Interventional Neuroradiology, UCLA Medical Center, Los Angeles, CA
  2. 2Division of Diagnostic Neuroradiology, UCLA Medical Center, Los Angeles, CA
  3. 3Department of Radiology, UCLA Medical Center, Los Angeles, CA
  4. 4Division of Laboratory Animal Medicine, UCLA Medical Center, Los Angeles, CA
  5. 5Department of Pathology, UCLA Medical Center, Los Angeles, CA
  6. 6Department of Neurology, UCLA Medical Center, Los Angeles, CA


Background and purpose A reliable animal model of ischemic stroke is vital for pre-clinical evaluation of stroke therapies. We describe a reproducible middle cerebral artery (MCA) embolic occlusion in the French Lop rabbit characterized with multimodal MRI and histopathologic tissue analysis.

Methods Fluoroscopic-guided microcatheter placement was performed in five consecutive subjects with angiographic confirmation of MCA occlusion with autologous clot. Multimodal MRI was obtained prior to occlusion and up to six hours post after which repeat angiography confirmed sustained occlusion. The brain was harvested for histopathologic examination.

Results Angiography confirmed successful MCA catheterization and durable (>6 hour) MCA occlusion in all animals. There was increase of ADC volume over time and variable final core volume presumably related to individual variation in collateral flow. FLAIR hyperintensity indicative of cytotoxic edema and parenchymal contrast enhancement reflective of blood brain barrier disruption was observed over time. Tissue staining of the ischemic brain showed edema and structural alterations consistent with infarction.

Conclusions We demonstrate the feasibility of a rabbit model of embolic MCA occlusion with angiographic documentation. Serial MR imaging demonstrated changes comparable to those observed in human ischemic stroke, confirmed histopathologically.

Disclosures R. Jahan: None. P. Villablanca: None. R. Harris: None. S. Duarte-Vogel: None. C. Williams: None. H. Vinters: None. N. Rao: None. D. Enzmann: None. B. Ellingson: None.

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