The purpose of this experiment was to determine the disposition of D-tagato
se, under development as a low-calorie sweetener, in conventional and germ-
free male rats. One group of conventional rats was fed a diet containing D-
tagatose (100 g/kg) mixed with the nonpurified diet (900 g/kg) for 28 days.
Then, [U-C-14]-labeled D-tagatose was administered as a single dose (appro
ximately 220-380 kBq) to 4 of these adapted rats, as well as to 15 conventi
onal and germ-free rats with no prior exposure (i.e., unadapted) to D-tagat
ose, Eleven of the 19 dosed animals (4 adapted conventional, 3 unadapted co
nventional and 2 unadapted germ-free, all dosed orally, plus 2 unadapted co
nventional dosed intravenously) were placed in metabolism chambers and samp
les of CO2, urine, and feces taken at regular intervals. At termination, a
complete material balance was obtained based on the recovery of C-14. Over
the 6-h digestive period, D-tagatose was metabolized to release 39.9 and 13
.9% of the oral dose as CO2 in the adapted conventional rats and in the una
dapted germ-free rats, respectively. Total releases approximated 68 and 22%
, respectively. The difference in CO2 evolution is ascribed to microbial fe
rmentation of D-tagatose in the gut of the conventional rats. The role of a
daptation was confirmed by finding 93% less D-tagatose in the feces of the
adapted conventional rat than in the feces of the unadapted conventional ra
t. The intestinal absorption of D-tagatose in the rat is estimated to be 20
%. The results demonstrate that D-tagatose is metabolized primarily by micr
oorganisms in the gut of the rat, with an upper limit between 15 and 20% of
oral dose metabolized by the host. (C) 1999 Academic Press.