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All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.
1. Brain staining and slicing
- After the middle cerebral artery occlusion experiment, remove the brain, including the brainstem, from the skull, and wash it in ice-cold PBS.
- Choose the correct size of the brain stainless-steel matrix (see the Table of Materials) depending on the weight of the animals (Figure 1B). Place the brain with its ventral side up in the brain matrix.
NOTE: When seated in the matrix, the brain's ventral surface must be parallel to the top surface of the mold.
- Using blades, restrict the frontal and caudal parts (2 blades from both sides) of the brain.
NOTE: Slicing matrix-compatible razor blades must be used. In general, a compatible, single-edge razor blade (thickness of up to 0.01 inch (0.254 mm)) can be used for rat brain slicing.
- Put the blades partially (not fully cutting the brain) into the channels between the first and the last blades. When all the blades are inserted and arranged in parallel, press all the blades down with the palm at the same time to cut the brain into 2 mm coronal slices.
- Grasp the blades firmly along the sides with two fingers and remove them together with the sliced brain from the matrix.
- Arrange the brain slices one by one in a tray (70 mL, 72 x 72 mm). When arranging the slices, ensure that the anterior surface of each slice is always facing up.
- Pour warm (+37 °C) 1% TTC solution in PBS onto the brain slices and incubate them for 8 min at 37 °C in the dark.
NOTE: The brain slices must be fully immersed in TTC solution during the incubation.
- After incubation in 1% TTC solution, transfer the brain slices to the blue plastic tray to capture images. Arrange the brain slices in sequential order from the frontal to the caudal part and use a scalpel to separate the hemispheres in the sagittal plane.
