Rodent brain processing for histological analyses (update)
Miquel Vila
Abstract
Protocol for rat brain processing in order to perform histological analyses
Steps
Rat perfusion
Deeply anesthetize animals with sodium pentobarbital (50 mg/kg, i.p.)
Perfuse through the left ventricle with saline [0.9% (wt/vol)] at room temperature (RT)
Perfuse again with ice-cold formaldehyde solution 4% in PBS buffered for histology
Postfixation
Remove brains and post-fix them for 24 h in the same fixative
Processing for microtome sectioning
Wash twice with 0.1 M PBS and process for paraffin embedding following standard procedures (performed by an external facility)
Alternatively, brains could be stored in 0.1 M PBS at 4 °C (not for over a month without changing the PBS) prior paraffin processing
Processing for cryostat sectioning
Cryoprotect for 24-48 h (until they sink) in 30% sucrose at 4 °C
Exchange sucrose for 0.1 M PBS
Immerse brains in cold (-30ºC) 2-methylbutane for 30 s and store at -80 °C
Include in OCT
Sectioning
Perform sectioning with a sliding microtome at 5-μm-thickness for paraffin samples or
in a cryostat at 20- or 30-μm-thickness for frozen samples.