Rats bearing the Yoshida AH-130 ascites hepatoma, a cachectic rat tumo
ur, showed signs of important muscle wasting with reduced muscle weigh
ts. This phenomenon was associated with a decreased rate of in vivo al
anine oxidation as measured by the production of (CO2)-C-14 from [U-C-
14]alanine intragastrically administered. it was later found that the
decreased amino acid oxidation was associated with a reduced uptake in
skeletal muscle as measured in incubated soleus muscles, thus suggest
ing that the decreased in vivo oxidation is basically due to a reduced
oxidation of the amino acid in skeletal muscle. The decrease in alani
ne oxidation in the tumour-bearing animals was also associated with hi
gher circulating alanine concentrations in their blood. In addition, t
umour-bearing rats presented a lower (26%) protein synthetic rate in s
keletal muscle, as measured by the incorporation of [C-14]phenylalanin
e into muscle protein, The addition of insulin to the incubation mediu
m abolished the tower rate of protein synthesis, thus suggesting a gre
ater response to this hormone by the muscle of tumour-bearing rats. In
conjunction with a reduced protein synthesis, tumour-bearing rats sho
wed a clearly enhanced rate of protein degradation in isolated skeleta
l muscles. The results presented confirm previous observations suggest
ing that the skeletal muscle of tumour bearing animals is in a profoun
d negative nitrogen balance which partially accounts for the wasting o
bserved in the tissue. in addition, the present study allows us to con
clude that, in spite of the increased alanine utilization for both glu
coneogenesis and tumour growth, the oxidation of alanine by the whole
animal is decreased in the tumour-bearing rats. This seems to be assoc
iated with a decreased ability of skeletal muscle to handle this amino
acid.