Human gut microbiota does not ferment erythritol

被引:63
作者
Arrigoni, E [1 ]
Brouns, F
Amadò, R
机构
[1] ETH Zentrum, Inst Food Sci & Nutr, Swiss Fed Inst Technol ETH, CH-8092 Zurich, Switzerland
[2] Cerestar Cargill R&D Ctr, B-1800 Vilvoorde, Belgium
[3] Maastricht Univ, Nutr & Toxicol Res Inst, Maastricht, Netherlands
关键词
erythritol; maltitol; lactulose; in vitro fermentation;
D O I
10.1079/BJN20051546
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Erythritol, a naturally occurring polyol, is gaining attention as a bulk sweetener for human nutrition. Industrially, it is produced from glucose by fermentation. From various studies it is known to be non-cariogenic. Moreover, it is rapidly absorbed in the small intestine and quantitatively excreted in the urine. Only about 10% enters the colon. Earlier in vitro experiments showed that erythritol remained unfermented for a fermentation period of 12 h. In order to investigate whether fresh human intestinal microbiota is able to adapt its enzyme activities to erythritol, a 24 h lasting fermentation was carried out under well-standardised in vitro conditions. For comparison maltitol, lactulose and blank (faecal inoculum only) were incubated as well. Fermentation patterns were established by following total gas production, hydrogen accumulation, changes in pH value, SCFA production and substrate degradation. Taking all fermentation parameters into account, erythritol turned out to be completely resistant to bacterial attack within 24 h, thus excluding an adaptation within that period. Since under in vivo conditions more easily fermentable substrates enter the colon continuously, it seems very unlikely that erythritol will be fermented in vivo.
引用
收藏
页码:643 / 646
页数:4
相关论文
共 16 条
[1]  
ARRIGONI E, 2004, VAH ILSI JAP INT S N
[2]  
BARRY JL, 1992, 3492020 INRA STAT TE
[3]   Erythritol: A review of biological and toxicological studies [J].
Bernt, WO ;
Borzelleca, JF ;
Flamm, G ;
Munro, IC .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1996, 24 (02) :S191-S197
[4]   Plasma and urine kinetics of erythritol after oral ingestion by healthy humans [J].
Bornet, FRJ ;
Blayo, A ;
Dauchy, F ;
Slama, G .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1996, 24 (02) :S280-S285
[5]  
*EUR COMM SCI COMM, 2003, SCFCSADDEDUL215 EUR
[6]   Fermentation of non-digestible oligosaccharides by human colonic bacteria [J].
Gibson, GR ;
Willems, A ;
Reading, S ;
Collins, MD .
PROCEEDINGS OF THE NUTRITION SOCIETY, 1996, 55 (03) :899-912
[7]  
Goossens J., 1994, Food Science and Technology Today, V8, P144
[8]   METABOLISM OF ERYTHRITOL IN HUMANS - COMPARISON WITH GLUCOSE AND LACTITOL [J].
HIELE, M ;
GHOOS, Y ;
RUTGEERTS, P ;
VANTRAPPEN, G .
BRITISH JOURNAL OF NUTRITION, 1993, 69 (01) :169-176
[9]   Effects of oral administration of erythritol on patients with diabetes [J].
Ishikawa, M ;
Miyashita, M ;
Kawashima, Y ;
Nakamura, T ;
Saitou, N ;
Modderman, J .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1996, 24 (02) :S303-S308
[10]  
*ISO INT STAND, 1998, 10504 ISO