Uremia induces substantial changes in protein metabolism. The branched-chai
n amino acids serve as useful markers of these changes and their catabolism
is increased in uremia, particularly in the presence of metabolic act dosi
s. Glucocorticoids also are involved in accelerating protein degradation, a
nd the negative nitrogen balance which results in loss of lean body mass. C
ellular mechanisms accounting for these changes include an up-regulation of
the ubiquitin-proteasome pathway and branched-chain ketoacid dehydrogenase
activity in muscle. A low insulin level also appears to play a permissive
role in causing increased catabolism. These findings have important clinica
l implications because correction of the metabolic acidosis with alkali blu
nts these responses and improves nutritional status.