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Nutrition Research Center, Department of Physiology, St. John's Medical College, Bangalore 560034, India;
*
U.S. Department of Agriculture/ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX;
Department of Pediatrics, St. John's Medical College, Bangalore, India; and
**
U.S. Department of Agriculture, Washington, DC
3To whom correspondence and reprint requests should be addressed.
In disadvantaged populations, recurrent infections lead to a loss of
body nitrogen and worsen nutritional status. The resulting
malnutrition, in its turn, produces a greater susceptibility to
infection. This study aimed to examine the ability of a new minimally
invasive tracer protocol to measure leucine oxidation, and then to use
it to quantify the effect of vaccination on leucine kinetics and
oxidation. Undernourished men (n = 5; body mass
index 16.3 ± 0.9 kg/m2) and children
(n = 9; age 4.1 ± 0.6 y; weight-for-age
Z-score -2.3 ± 0.7) underwent metabolic studies 6 d
before and 1 d after vaccination with diphtheria, pertussis and
tetanus (DPT). The tracer protocol was performed in the fed state and
involved two 3-h sequential periods of frequent (20 min) oral doses of
NaH13CO3 or [1-13C] leucine.
Frequent breath samples and urine collections were made. Blood samples
were obtained from the men and used for the determination of the
isotopic enrichment of
-ketoisocaproic acid. The prevaccination
oxidation of leucine (percentage of dose ± SD) was
18.1 ± 2.3 (men) and 16.7 ± 3.8 (children). One day after
vaccination, these values had risen to 19.9 ± 1.9
(P < 0.05) in the men and to 19.5 ± 4.6
(P < 0.01) in the children. In the adults,
vaccination was associated with a rise in whole-body protein
breakdown [mg protein/(kg·h)] from 200 ± 40 to 240 ± 10
(P < 0.05). A minor simulated infection increases
leucine catabolism in undernourished humans and this new, minimally
invasive protocol is sufficiently sensitive to measure these
changes.
KEY WORDS: infection protein metabolism undernourished humans stable isotopes
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