Abstract
In the steady state, the ratio of the rate of utilization for whole-body protein synthesis of any essential amino acid to its rate of oxidation should be the same as the ratio of the peak fraction of a dose of tracer incorporated into protein (F) to the fraction oxidized (1-F) provided that negligible tracer remains in the free amino acid pool or remains unabsorbed in the gut. The total rate of amino acid catabolism (C) can be estimated from the rate of urinary excretion of urea nitrogen (N) plus ammonia N. Hence the rate of whole-body protein synthesis (S) can be estimated as CF (1 − F) . This method, which is not new, was explored as follows: (1) Radioactivity in the leucine of whole-body protein of rats after intravenous (IV) injection of labeled leucine was shown to plateau from three to nine hours. (2) The fractions of labeled leucine, valine, and methionine remaining in the gut six hours after enteral injection were 1.2 ± 0.4% (SD), 1.2 ± 0.4%, and 7.1 ± 2.9%, respectively; thus, enterally administered methionine cannot be used for this purpose. (3) Oxidation of [1- 14C]-labeled leucine or valine, measured from 14CO 2 excretion, was found to be the same whether these isotopes were given IV or enterally. (4) Negligible radioactivity remained in the free leucine of plasma within one hour after injection of labeled leucine. (5) The rates of whole-body protein synthesis, estimated from cumulative 14CO 2 excretion for six hours after enteral or IV injection of [1- 14C]-labeled leucine or valine, or after IV injection of [1- 14C]-labeled methionine did not differ from one another by more than 7%. Mean S was 73 mg 100 g body wt/h . These results support the validity of this technique for determining whole-body protein synthesis.
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