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松二糖对小鼠的急性和13周亚慢性毒理学评价。

Acute and 13-week subchronic toxicological evaluations of turanose in mice.

作者信息

Chung Joo-Yeon, Lee Jihye, Lee Daeyeon, Kim Eunju, Shin Jae-Ho, Seok Pu Reum, Yoo Sang-Ho, Kim Yuri

机构信息

Department of Nutritional Science and Food Management, Ewha Womans University, 52 Ewhayeodae-gil, Seodaemun-gu, Seoul 03760, Korea.

Department of Food Science and Biotechnology, and Carbohydrate Bioproduct Research Center, Sejong University, 209 Neungdong-ro, Gwangjin-gu, Seoul 05006, Korea.

出版信息

Nutr Res Pract. 2017 Dec;11(6):452-460. doi: 10.4162/nrp.2017.11.6.452. Epub 2017 Nov 24.

Abstract

BACKGROUND/OBJECTIVES: Turanose, α-D-glucosyl-(1→3)-α-D-fructose, is a sucrose isomer which naturally exists in honey. To evaluate toxicity of turanose, acute and subchronic oral toxicity studies were conducted with ICR mice.

MATERIALS AND METHODS

For the acute oral toxicity study, turanose was administered as a single oral dose [10 g/kg body weight (b.w.)]. In the subchronic toxicity study, ICR mice were administered 0, 1.75, 3.5, and 7 g/kg b.w. doses of turanose daily for 13 weeks.

RESULTS

No signs of acute toxicity, including abnormal behavior, adverse effect, or mortality, were observed over the 14-day study period. In addition, no changes in body weight or food consumption were observed and the median lethal dose (LD) for oral intake of turanose was determined to be greater than 10 g/kg b.w. General clinical behavior, changes in body weight and food consumption, absolute and relative organ weights, and mortality were not affected in any of the treatment group for 13 weeks. These doses also did not affect the macroscopic pathology, histology, hematology, and blood biochemical analysis of the mice examined.

CONCLUSION

No toxicity was observed in the acute and 13-week subchronic oral toxicology studies that were conducted with ICR mice. Furthermore, the no-observed-adverse-effect level is greater than 7 g/kg/day for both male and female ICR mice.

摘要

背景/目的:松三糖,α-D-葡糖基-(1→3)-α-D-果糖,是一种天然存在于蜂蜜中的蔗糖异构体。为评估松三糖的毒性,对ICR小鼠进行了急性和亚慢性经口毒性研究。

材料与方法

在急性经口毒性研究中,以单次经口剂量[10克/千克体重(b.w.)]给予松三糖。在亚慢性毒性研究中,ICR小鼠每天分别给予0、1.75、3.5和7克/千克b.w.剂量的松三糖,持续13周。

结果

在为期14天的研究期间,未观察到急性毒性迹象,包括异常行为、不良反应或死亡。此外,未观察到体重或食物摄入量的变化,经口摄入松三糖的半数致死剂量(LD)被确定大于10克/千克b.w.。在13周的时间里,任何治疗组的一般临床行为、体重和食物摄入量的变化、绝对和相对器官重量以及死亡率均未受到影响。这些剂量也未影响所检查小鼠的大体病理学、组织学、血液学和血液生化分析。

结论

在用ICR小鼠进行的急性和为期13周的亚慢性经口毒理学研究中未观察到毒性。此外,对于雄性和雌性ICR小鼠,未观察到有害作用水平均大于7克/千克/天。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437e/5712495/e231382d32fa/nrp-11-452-g001.jpg

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