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Articles in PresS, published online ahead of print April 5, 2002
J Appl Physiol, 10.1152/jap.01195.2001
Submitted on December 4, 2001
Accepted on April 2, 2002
1 Department of Kinesiologie, Universite de Montreal, Montreal, Quebec, Canada
2 Department of Kinanthropologie, Universite du Quebec a Montreal, Montreal, Quebec, Canada
3 Department des sciences de l'activite physique, Universite du Quebec a Trois Rivieres, Trois-Rivieres, Quebec, Canada
* To whom correspondence should be addressed. E-mail: francois.peronnet{at}umontreal.ca.
The decarboxylation/oxidation and the deamination of 13C- and 15N-alanine ingested (1 g/kg or 73.7 ± 2 g) during prolonged exercise at low workload (180 min at 53 ± 2 %VO2max) was measured in six healthy male subjects from V13CO2 at the mouth and 15N-urea excretion in urine and sweat. Over the exercise period, 50.6 ± 3.5 g of exogenous alanine were oxidized (68.7 ± 4.5 % of the load), providing 10.0 ± 0.6 % of the energy yield vs 4.8 ± 0.4, 47.6 ± 4.3, and 37.4 ± 4.7 % for endogenous proteins, glucose and lipids, respectively. Alanine could have been oxidized following conversion into glucose in the liver and/or directly in peripheral tissues. In contrast, only 13.0 ± 3.2 mmol of 15N-urea were excreted in urine and sweat (10.6 ± 0.4 and 2.4 ± 0.5 mmol, respectively) corresponding to the deamination of 2.3 ± 0.3 g of exogenous alanine (3.1 ± 0.4 % of the load). These results confirm that the metabolic fate of the carbon skeleton and the amino-N moiety of exogenous alanine ingested during prolonged exercise at low workload are markedly different. The large positive nitrogen balance (8.5 ± 0.3 g) suggests that in this situation protein synthesis could be increased when a large amount of a single amino-acid is ingested.
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