Subchronic oral toxicity studies with γ-cyclodextrin in rats

被引:17
作者
Lina, BAR
Bar, A
机构
[1] Bioresco AG, CH-4102 Binningen, Switzerland
[2] TNO, Nutr & Food Res Inst, NL-3700 AJ Zeist, Netherlands
关键词
D O I
10.1006/rtph.1998.1223
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
The toxicity of gamma-cyclodextrin ( gamma-CD), a cyclic polymer of eight alpha-1,4-linked glucopyranosyl units with potential applications as a food ingredient, was examined in a 2-week pilot study followed by a 13-week oral toxicity study in Wistar rats. In the 2-week study, the test substance was administered to groups of 5 male rats at dietary levels of 0, 5, 10, 15, and 20%. In the 13-week study, groups of 20 rats/sex received diets with 0, 1.5, 5, or 20% gamma-CD. In each study, a comparison group receiving a diet with 20% lactose also was included. The 13-week study also included satellite groups of 10 rats/sex for the control and 20% gamma-CD groups. These satellite groups were kept on a standard, cereal-based rodent diet for a 4-week recovery period after termination of the treatment period. Parameters measured during the two studies were clinical signs, body weights, food and water intake, clinicochemical parameters, organ weights, and gross observation at necropsy. In the 13-week study, ophthalmoscopic and hematological examinations, urine and feces analyses, and histopathological examination of standard organs and tissues were conducted. There were no treatment-related mortalities in either study. Soft stools and, in the 13-week study, infrequent occurrences of diarrhea were noted in the lactose group at the beginning of treatment. Among the gamma-CD groups, soft stools occurred in only a few animals of the high-dose groups (greater than or equal to 10% gamma-CD) during the first few days of treatment. Mean body weights tended to be slightly reduced in males of the 20% gamma-CD and 20% lactose groups. However, food efficiency was not affected by treatment except in the 13-week study in males of the 20% gamma-CD group during the first week of treatment. The hematological examinations and the semiquantitative urinalyses (conducted in the 13-week study) and the clinicochemical investigations (both studies) did not reveal any changes that could be attributed to gamma-CD treatment. Except for a slight cecal enlargement, which is commonly observed in rodents upon ingestion of incompletely absorbed carbohydrates, organ weights did not exhibit relevant changes as a result of gamma-CD treatment. On histopathological examination (13-week study), no treatment-related abnormalities were found. In conclusion, the ingestion of gamma-CD for 13 weeks at dietary levels of up to 20% (corresponding to intakes of 11.4 and 12.7 g/kg body wt/day for male and female rats, respectively) was well tolerated and did not produce any signs of toxicity. (C) 1998 Academic Press.
引用
收藏
页码:178 / 188
页数:11
相关论文
共 31 条
[1]  
Allegre M., 1994, Agro Food Industry hi-tech, V5, P9
[2]   NUTRITIONAL ROLE OF RESISTANT STARCH - CHEMICAL-STRUCTURE VS PHYSIOLOGICAL-FUNCTION [J].
ANNISON, G ;
TOPPING, DL .
ANNUAL REVIEW OF NUTRITION, 1994, 14 :297-320
[3]  
[Anonymous], 1983, PHARMACOMETRICS
[4]  
[Anonymous], COMPREHENSIVE SUPERM
[5]   SUGARS AND ADRENOMEDULLARY PROLIFERATIVE LESIONS - THE EFFECTS OF LACTOSE AND VARIOUS POLYALCOHOLS [J].
BAER, A .
JOURNAL OF THE AMERICAN COLLEGE OF TOXICOLOGY, 1988, 7 (01) :71-81
[6]   SAFETY ASSESSMENT OF POLYOL SWEETENERS - SOME ASPECTS OF TOXICITY [J].
BAR, A .
FOOD CHEMISTRY, 1985, 16 (3-4) :231-241
[7]   BACTERIAL TOXICITY OF CYCLODEXTRINS - LUMINOUS ESCHERICHIA-COLI AS A MODEL [J].
BAR, R ;
ULITZUR, S .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1994, 41 (05) :574-577
[8]   BETA-CYCLODEXTRIN - 52-WEEK TOXICITY STUDIES IN THE RAT AND DOG [J].
BELLRINGER, ME ;
SMITH, TG ;
READ, R ;
GOPINATH, C ;
OLIVIER, P .
FOOD AND CHEMICAL TOXICOLOGY, 1995, 33 (05) :367-376
[9]   DIGESTION + ABSORPTION OF LACTOSE BY INTACT RAT [J].
DAHLQVIST, A ;
THOMSON, DL .
ACTA PHYSIOLOGICA SCANDINAVICA, 1964, 61 (1-2) :20-&
[10]  
DEBIE ATH, 1998, IN PRESS EGUL TOXICO, V27