Tagatose: from a sweetener to a new diabetic medication?

被引:45
作者
Espinosa, Ikna [1 ]
Fogelfeld, Leon [1 ]
机构
[1] Rush Univ, Med Ctr, John H Stroger Hosp Cook Cty, Chicago, IL 60612 USA
关键词
artificial sweetener; diabetes medication; hexose; postprandial hyperglycemia; sugar substitute; tagatose; IMPAIRED GLUCOSE-TOLERANCE; RAT HEPATOCYTES; D-FRUCTOSE; POSTPRANDIAL HYPERGLYCEMIA; URIC-ACID; TRANSLOCATION; GLUCOKINASE; DIGESTIBILITY; STEREOISOMER; PATHOGENESIS;
D O I
10.1517/13543780903501521
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Importance of the field. Tagatose is a naturally occurring simple sugar that is a more palatable bulk low-calorie (1.5 kcal/g) sweetener. It was approved as a food additive by the FDA in 2003. Tagatose has been studied as a potential antidiabetic and antiobesity medication. In preliminary studies in humans, tagatose has shown a low postprandial blood glucose and insulin response. Its proposed mechanism of action may involve interference in the absorption of carbohydrates by inhibiting intestinal disaccharidases and glucose transport. It may also act through hepatic inhibition of glycogenolysis. Areas covered in this review. This article summarizes tagatose Phase I and II diabetes trials. It describes the pharmacodynamics and possible mechanism of action of this agent. Literature from 1974 to 2009 is reviewed. What the reader will gain: Better understanding of the implications of postprandial hyperglycemia. An appreciation of the liver as a target of glucose control. Increased awareness of tagatose, a sweetener, as a potential new medication that operates through improvement of postprandial hyperglycemia. Take home message: Tagatose is currently being studied as a postprandial anti hyperglycemic agent that may be safer with regard to hypoglycemia. Ongoing Phase III clinical trials will provide more definitive answers.
引用
收藏
页码:285 / 294
页数:10
相关论文
共 55 条
[1]  
*AACE, 2003, STAT DIAB AM EX SUMM
[2]   The physiological role of glucokinase binding and translocation in hepatocytes [J].
Agius, L .
ADVANCES IN ENZYME REGULATION, VOL 38, 1998, 38 :303-331
[3]   Evidence for a role of glucose-induced translocation of glucokinase in the control of hepatic glycogen synthesis [J].
Agius, L ;
Peak, M ;
Newgard, CB ;
GomezFoix, AM ;
Guinovart, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (48) :30479-30486
[4]   CONTROL OF GLUCOKINASE TRANSLOCATION IN RAT HEPATOCYTES BY SORBITOL AND THE CYTOSOLIC REDOX STATE [J].
AGIUS, L .
BIOCHEMICAL JOURNAL, 1994, 298 :237-243
[5]   Characteristics and significance of D-tagatose-induced liver enlargement in rats:: An interpretative review [J].
Bär, A .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1999, 29 (02) :S83-S93
[6]   Effect of D-tagatose on liver weight and glycogen content of rats [J].
Bär, A ;
Lina, BAR ;
de Groot, DMG ;
de Bie, B ;
Appel, MJ .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1999, 29 (02) :S11-S28
[7]  
Bastarrachea RA, 2008, REV MED CHILE, V136, P107, DOI /S0034-98872008000100014
[8]  
Bertelsen Hans, 2001, Microbial Ecology in Health and Disease, V13, P87, DOI 10.1080/089106001300136147
[9]   Effect of oral D-tagatose on liver volume and hepatic glycogen accumulation in healthy male volunteers [J].
Boesch, C ;
Ith, M ;
Jung, B ;
Bruegger, K ;
Erban, S ;
Diamantis, I ;
Kreis, R ;
Bär, A .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2001, 33 (02) :257-267
[10]  
BOLLEN M, 1983, BIOCHEM BIOPH RES CO, V15, P1033