The oxidation of several metabolites in AS-30D tumor cells was determined.
Glucose and glycogen consumption and lactic acid production showed high rat
es, indicating a high glycolytic activity. The utilization of ketone bodies
, oxidation of endogenous glutamate, and oxidative phosphorylation were als
o very active: tumor cells showed a high respiration rate (100 ng atoms oxy
gen (min x 10(7) cells)(-1)), which was 90% oligomycin-sensitive. AS-30D tu
mor cells underwent significant intracellular volume changes, which preserv
ed high concentrations of several metabolites. A high O-2 concentration, bu
t a low glucose concentration were found in the cell-free ascites liquid. G
lutamine was the oxidizable substrate found at the highest concentration in
the ascites liquid. We estimated that cellular ATP was mainly provided by
oxidative phosphorylation. These data indicated that AS-30D hepatoma cells
had a predominantly oxidative and not a glycolytic type of metabolism. The
NADH-ubiquinol oxide reductase and the enzyme block for ATP utilization mer
e the sites that exerted most of the control of oxidative phosphorylation (
flux control coefficient 01.3-0.42). (C) 2000 Academic Press.