4-WEEK ORAL TOXICITY STUDY WITH ERYTHRITOL IN RATS

Citation
Hp. Til et J. Modderman, 4-WEEK ORAL TOXICITY STUDY WITH ERYTHRITOL IN RATS, Regulatory toxicology and pharmacology, 24(2), 1996, pp. 214-220
Citations number
12
Categorie Soggetti
Medicine, Legal","Pharmacology & Pharmacy",Toxicology
ISSN journal
02732300
Volume
24
Issue
2
Year of publication
1996
Part
2
Pages
214 - 220
Database
ISI
SICI code
0273-2300(1996)24:2<214:4OTSWE>2.0.ZU;2-S
Abstract
Erythritol was orally administered to Wistar rats at dietary levels of 0, 5, and 10% for 4 weeks. Soft stools and diarrhea were observed in male and female animals of the 10% group and in female animals of the 5% group. These symptoms disappeared during the course of the study. M ean body weights of male rats in the high-dose group were significantl y lower than those of controls during the course of the study. No such differences were observed in females. Small statistically significant changes in certain hematological, clinical chemistry, and urine param eters were noted in the high-dose group but were judged not to be biol ogically important. Weights of the cecum were increased relative to th ose of the controls. No treatment-related histological changes were ob served. No ill effects, other than early diarrhea, were observed from erythritol levels at 5 or 10% in the diet. Eased on these results, it was concluded that the feeding of erythritol at a dietary level of 10% did not result in toxicologically significant effects. (C) 1996 Acade mic Press, Inc.