B. Messing et al., Whole-body protein metabolism assessed by leucine and glutamine kinetics in adult patients with active celiac disease, METABOLISM, 47(12), 1998, pp. 1429-1433
To assess the effect of increased renewal of intestinal epithelial cells on
leucine and glutamine (Gln) turnover. 4-hour intravenous infusions of L-[1
-C-13]leucine and L-[2-N-15]Gln were administered to five adult patients wi
th active celiac disease in the postabsorptive state. There was a 35% incre
ase in leucine flux (micromoles per kilogram per hour) in patients (117 +/-
17) compared with healthy controls (96 +/- 11, P < .03). Gin flux was incr
eased by 13% in patients (377 +/- 35) versus controls (335 +/- 16, P < .04)
. These results suggest that active celiac disease, characterized by villou
s atrophy and crypt cell hyperplasia, is associated with a dramatic increas
e in whole-body protein breakdown as assessed by C-13-leucine, which may co
ntribute per se to the protein malnutrition status of the patients. The inc
rease in Gin utilization as assessed by L-[2-N-15]Gln was moderate. but may
have been offset due to the villose atrophy and ensuing reduced intestinal
epithelial cell mass. The results are consistent with the concept that inc
reased renewal of intestinal epithelial cells represents a sizable fraction
of whole-body protein turnover and that Gin is an important fuel for epith
elial intestinal cells in vivo. Copyright (C) 1998 by W.B. Saunders Company
.