The amount of energy mobilized or stored as protein, expressed as a pr
oportion of the total energy stored or mobilized (defined as the P rat
io, Payne & Dugdale, 1977), was investigated in the young male (rapid
growth) and adult female (slow growth) rat. Energy mobilization was in
duced by a 3 d fast and the changes in body content of fat and lean ti
ssues were used to estimate the fasting P ratio (P-fast). Tissue stora
ge was subsequently effected by 17 d of refeeding and the correspondin
g ratio (P-refed) was calculated from the amounts of lean and fat tiss
ue regained. The same experimental protocol was used for measuring P-f
ast and P-refed in weanling (30 d) and adult (130 d) rats. Weight-matc
hed individuals were assigned to three groups. All animals in group 1
were killed at the beginning of the experiment. Animals in group 2 wer
e fasted for 30 and then killed. Group 3 animals were first fasted for
3 d, then had free access to a stock diet for a further 17 d before b
eing killed. During fasting, a close linear relationship was found bet
ween weight change and body energy changes (r 0.985, and r 0.92, P < 0
.001 for weanlings and adult rats respectively) and between carcass N
loss and urinary N loss (r 0.933, P < 0.001). These relationships were
used to estimate the body energy and N content of each animal at the
end of the initial fasting period. Hence, both P-fast and P-refed valu
es could be calculated for all individuals at both ages. When P-fast a
nd P-refed were calculated for adult rats, the mean values were simila
r (0.138 (SE 0.002) and 0.130 (SE 0.006) respectively). Individually,
the P-fast and P-refed values were correlated (r 0.54, P = 0.058). In
weanling rats, the mean P-refed value was about 2.5 times the P-fast (
0.421 (SE 0.0113) v. 0.156 (SE 0.004)). Despite the differences in P-f
ast and P-refed, the individual values were again correlated (r 0.668,
P < 0.05). These results support the suggestion made by Payne & Dugda
le (1977), that particular P-ratio values are characteristic of indivi
duals and describe the extent to which protein is mobilized or stored
during fasting or refeeding. These observations are discussed in relat
ion to the predictions made by the Payne-Dugdale model.