1. Primary cultures of isolated sheep hepatocytes were used to charact
erize metabolic functions of liver: gluconeogenesis, ureagenesis and p
rotein synthesis. The rates of all three metabolic activities were lin
ear over a 20 hr culture period. 2. Hepatocytes in the presence of glu
cagon increased the synthesis of urea by approx 30% (P < 0.05) and inc
reased release of glucose into the medium by 60% (P < 0.05). 3. In the
absence of insulin, significantly more (35%; P < 0.05) glucose was re
leased in the medium than in the presence of insulin. 4. Results help
evaluate the primary culture of sheep hepatocytes as an appropriate ex
perimental model to study nutritional and hormonal regulation of liver
in the ruminant species.