Portal vein perfusion of
rat's
liver was carried out with
Ringer's solution followed by 2.5 per cent
glutaraldehyde.
Liver samples were postifixed in
osmium tetroxide, washed in
distilled water, snap-frozen in
Freon-12, and fractured at -150§C. After freeze-drying at -80§C., a thin layer of
carbon and
gold was applied under
vacuum. Under the scanning
electron microscope, the sinusoidal fenestrations and the relationships of the
endothelial cells to
hepatocyte microvilli and
reticulin fibres were delineated. Images of
bile canaliculi and adjoining
plasma membranes were obtained. These
techniques have great potential for the study of a variety of
liver diseases. (AU)