• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Disposition of 14C-erythritol in germfree and conventional rats.

作者信息

Van Ommen B, de Bie B, Bär A

机构信息

TNO-CIVO Institutes, Zeist, The Netherlands.

出版信息

Regul Toxicol Pharmacol. 1996 Oct;24(2 Pt 2):S198-205. doi: 10.1006/rtph.1996.0099.

DOI:10.1006/rtph.1996.0099
PMID:8933634
Abstract

The metabolism and disposition of U-14C-erythritol was examined in four groups of three male and three female, nonfasted rats each. The rats of groups A and D were germfree; the rats of groups B and C were kept under conventional conditions. The rats of group B received an erythritol-supplemented diet for 3 weeks prior to the experiment (adapted rats). The rats of groups A, C, and D were kept on an ordinary diet which was sterile for groups A and D (not adapted rats). On the day of the experiment, each rat was dosed with U-14C-erythritol by gavage (5 microCi/kg body wt; sp act 50 microCi/g erythritol). The radiochemical purity of the erythritol was 96.43% for groups A-C. Group D, which was attached to the study after evaluation of the results of groups A-C, received a more purified erythritol with a radiochemical purity of 99.46% because the data of group A pointed to a possible interference by a 14C-labeled impurity in the commercial 14C-erythritol. After dosing, respiratory CO2 and urine were collected from each rat at regular intervals for 24 hr. At termination, feces were also collected. The animals were killed and intestinal contents, organs, tissues, and the remaining carcass processed for determination of 14C-14C was excreted rapidly in the urine of all groups (range of groups A-D: 47.3-60.6% of the administered dose within the first 4 hr). Total 24-hr urinary excretion varied between 67.0% (group B) and 81.4% (group D). HPLC analysis of the urine showed that more than 96% of the eluted radiolabel represented erythritol. Conventional, adapted rats expired more 14CO2 than conventional, unadapted rats [10.9% (B) vs 6.7% (C)]. Germfree rats expired much less 14CO2 [0.8% (A) and 0.3% (D)]. In germfree rats, 14CO2 expiration started shortly after dosing, reaching half of the 24-hr excretion after about 2.5 hr. In conventional rats 14CO2 expiration started with a delay of about 2 hr reaching half the 24-hr excretion after 4-6 hr. The excretion of 14C with feces was similar in all groups (8.3% on average of all rats). Slightly more 14C was retained in the intestinal contents of germfree than conventional rats (1.9 vs 0.5%). The body retention was higher in conventional than in germfree rats (3.4 vs 2.0%). In group D, body retention was lowest (1.6%). The total recovery of 14C was similar in all groups (95.6%, average of all rats). It is concluded that ingested erythritol is efficiently absorbed mainly from the small intestine, is not metabolized to a relevant extent in the body, and is excreted unchanged in the urine. The fraction of erythritol not absorbed is fermented by the gut microflora to intermediate products which are largely absorbed and metabolized. The data support a proposed physiological energy value for erythritol of about 0.5 kcal/g.

摘要

相似文献

1
Disposition of 14C-erythritol in germfree and conventional rats.
Regul Toxicol Pharmacol. 1996 Oct;24(2 Pt 2):S198-205. doi: 10.1006/rtph.1996.0099.
2
Disposition of [14C]gamma-cyclodextrin in germ-free and conventional rats.[14C]γ-环糊精在无菌大鼠和普通大鼠体内的处置情况。
Regul Toxicol Pharmacol. 1998 Apr;27(2):150-8. doi: 10.1006/rtph.1998.1219.
3
Metabolism and disposition of erythritol after oral administration to rats.
J Nutr. 1992 Jun;122(6):1266-72. doi: 10.1093/jn/122.6.1266.
4
Disposition of 14C-alpha-cyclodextrin in germ-free and conventional rats.14C-α-环糊精在无菌大鼠和普通大鼠体内的处置情况。
Regul Toxicol Pharmacol. 2004 Jun;39 Suppl 1:57-66. doi: 10.1016/j.yrtph.2004.05.011.
5
Fate of erythritol after single oral administration to rats and dogs.
Regul Toxicol Pharmacol. 1996 Oct;24(2 Pt 2):S206-13. doi: 10.1006/rtph.1996.0100.
6
Disposition of D-[U-14C]tagatose in the rat.D-[U-14C]塔格糖在大鼠体内的处置情况。
Regul Toxicol Pharmacol. 1999 Apr;29(2 Pt 2):S46-56. doi: 10.1006/rtph.1998.1251.
7
Utilization and excretion of a new sweetener, fructooligosaccharide (Neosugar), in rats.新型甜味剂低聚果糖(益寿糖)在大鼠体内的利用与排泄情况
J Nutr. 1989 Apr;119(4):553-9. doi: 10.1093/jn/119.4.553.
8
Subchronic oral toxicity studies with erythritol in mice and rats.赤藓糖醇对小鼠和大鼠的亚慢性经口毒性研究。
Regul Toxicol Pharmacol. 1996 Oct;24(2 Pt 2):S221-31. doi: 10.1006/rtph.1996.0102.
9
The fate of ingested glyceran esters of condensed castor oil fatty acids [polyglycerol polyricinoleate (PGPR)] in the rat.大鼠摄入的蓖麻油脂肪酸甘油酯(聚甘油聚蓖麻醇酸酯,PGPR)的代谢情况。
Food Chem Toxicol. 1998 Sep-Oct;36(9-10):719-38. doi: 10.1016/s0278-6915(98)00055-6.
10
Chronic toxicity and carcinogenicity study of erythritol in rats.赤藓糖醇对大鼠的慢性毒性和致癌性研究。
Regul Toxicol Pharmacol. 1996 Oct;24(2 Pt 2):S264-79. doi: 10.1006/rtph.1996.0108.

引用本文的文献

1
Re-evaluation of erythritol (E 968) as a food additive.赤藓糖醇(E 968)作为食品添加剂的重新评估。
EFSA J. 2023 Dec 20;21(12):e8430. doi: 10.2903/j.efsa.2023.8430. eCollection 2023 Dec.
2
Effects of Sweeteners on the Gut Microbiota: A Review of Experimental Studies and Clinical Trials.甜味剂对肠道微生物群的影响:实验研究和临床试验综述。
Adv Nutr. 2019 Jan 1;10(suppl_1):S31-S48. doi: 10.1093/advances/nmy037.
3
Erythritol Is More Effective Than Xylitol and Sorbitol in Managing Oral Health Endpoints.赤藓糖醇在管理口腔健康指标方面比木糖醇和山梨醇更有效。
Int J Dent. 2016;2016:9868421. doi: 10.1155/2016/9868421. Epub 2016 Aug 21.