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Establishment of a reproducible and minimally invasive ischemic stroke model in swine
Carlos Castaño, Marc Melià-Sorolla, Alexia García-Serran, Núria DeGregorio-Rocasolano, Maria Rosa García-Sort, María Hernandez-Pérez, Adrián Valls-Carbó, Osvaldo Pino, Jordi Grífols, Alba Iruela-Sánchez, Alicia Palomar-García, Josep Puig, Octavi Martí-Sistac, Antoni Dávalos, Teresa Gasull
Carlos Castaño, Marc Melià-Sorolla, Alexia García-Serran, Núria DeGregorio-Rocasolano, Maria Rosa García-Sort, María Hernandez-Pérez, Adrián Valls-Carbó, Osvaldo Pino, Jordi Grífols, Alba Iruela-Sánchez, Alicia Palomar-García, Josep Puig, Octavi Martí-Sistac, Antoni Dávalos, Teresa Gasull
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Resource and Technical Advance Neuroscience

Establishment of a reproducible and minimally invasive ischemic stroke model in swine

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Abstract

The need for advances in the management/treatment options for ischemic stroke patients requires that upcoming preclinical research uses animals with more human-like brain characteristics. The porcine brain is considered appropriate, although the presence of the rete mirabile (RM) prevents direct catheterization of the intracranial arteries to produce focal cerebral ischemia. To develop a reproducible minimally invasive porcine stroke model, a guide catheter and guide wire were introduced through the femoral artery until reaching the left RM. Using the pressure cooker technique, Squid-12 embolization material was deposited to fill, overflow, and occlude the left RM, the left internal carotid artery, and left circle of Willis wing up to the origins of the middle cerebral arteries (MCAs), mimicking the occlusion produced in the filament model in rodents. Longitudinal multimodal cerebral MRI was conducted to assess the brain damage and cerebral blood supply. The technique we describe here occluded up to the origins of the MCAs in 7 of 8 swine, inducing early damage 90 minutes after occlusion that later evolved to a large cerebral infarction and producing no mortality during the intervention. This minimally invasive ischemic stroke model in swine produced reproducible infarcts and shows translational features common to human stroke.

Authors

Carlos Castaño, Marc Melià-Sorolla, Alexia García-Serran, Núria DeGregorio-Rocasolano, Maria Rosa García-Sort, María Hernandez-Pérez, Adrián Valls-Carbó, Osvaldo Pino, Jordi Grífols, Alba Iruela-Sánchez, Alicia Palomar-García, Josep Puig, Octavi Martí-Sistac, Antoni Dávalos, Teresa Gasull

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Figure 6

Brain perfusion impairment assessed through DSC-perfusion MRI.

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Brain perfusion impairment assessed through DSC-perfusion MRI.
(A) Repre...
(A) Representative relative cerebral blood volume images 90 minutes and 1 day after stroke induction in 2 axial levels (1 and 2, as indicated in the drawing on the left). (B). Image 1 shows (in yellow) the area of brain infarction measured in DWI at 90 minutes; image 2 shows (in blue) a map of brain tissue with a time-to-peak (TTP) greater than 40 seconds obtained 90 minutes after the stroke onset; image 3 shows (in red) the maximum area of infarct measured 1 day after the ischemia onset. (C) Histogram showing the number of voxels as a function of TTP in infarcted tissue (fuchsia bars) and healthy specular contralateral ROI (gray bars) 90 minutes after occlusion. The TTP > 40 threshold was selected by comparing the number of voxels in both healthy and infarcted tissue for each given TTP time point. Most healthy tissue voxels show a TTP of 36–38 seconds, whereas voxels in the infarcted areas depict a TTP greater than 40 seconds; a TTP delay of 4 seconds might mark compromised tissue.

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ISSN 2379-3708

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