Disposition of D-[U-C-14]tagatose in the rat

Citation
Jp. Saunders et al., Disposition of D-[U-C-14]tagatose in the rat, REGUL TOX P, 29(2), 1999, pp. S46-S56
Citations number
16
Categorie Soggetti
Pharmacology & Toxicology
Journal title
REGULATORY TOXICOLOGY AND PHARMACOLOGY
ISSN journal
02732300 → ACNP
Volume
29
Issue
2
Year of publication
1999
Part
2
Supplement
S
Pages
S46 - S56
Database
ISI
SICI code
0273-2300(199904)29:2<S46:DODITR>2.0.ZU;2-3
Abstract
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.