Oku T, Tokunaga T, Hosoya N
J Nutr. 1984 Sep;114(9):1574-81. doi: 10.1093/jn/114.9.1574.
The digestion of Neosugar, a mixture of 1F-(1-beta-fructofuranosyl)n-1 sucrose [n = 2, 1-kestose (GF2); n = 3, nystose (GF3); n = 4, 1F-beta-fructofuranosyl nystose (GF4)] was investigated in vitro and in vivo by using the rat. The results obtained were as follows. GF2 and GF3 were not hydrolyzed by a pancreatic homogenate. The GF2- and GF3-hydrolyzing activities of the enzymes in the intestinal mucosa homogenate were negligible compared with the activities of maltase and sucrase. GF2 and GF3 added to the incubation mixture did not affect the activities of sucrase and maltase in the intestinal mucosa. Long-term ingestion of Neosugar did not cause induction or suppression of GF2- and GF3-hydrolyzing enzymes in the small intestine. [U-14C]Neosugar injected intravenously was rapidly excreted in the urine without having undergone any degradation. These results indicate that Neosugar, which consists of GF2, GF3 and GF4, is scarcely hydrolyzed by the digestive enzymes of the gastrointestinal tract and internal organs, and that suggests to us that Neosugar is not utilized as an energy source in the body.
利用大鼠对低聚果糖(一种由1F-(1-β-D-呋喃果糖基)-n-1蔗糖组成的混合物[n = 2,1-蔗果三糖(GF2);n = 3,蔗果四糖(GF3);n = 4,1F-β-D-呋喃果糖基蔗果四糖(GF4)])的消化情况进行了体内和体外研究。得到的结果如下。GF2和GF3不被胰腺匀浆水解。与麦芽糖酶和蔗糖酶的活性相比,肠黏膜匀浆中酶的GF2和GF3水解活性可忽略不计。添加到孵育混合物中的GF2和GF3不影响肠黏膜中蔗糖酶和麦芽糖酶的活性。长期摄入低聚果糖不会导致小肠中GF2和GF3水解酶的诱导或抑制。静脉注射的[U-¹⁴C]低聚果糖未经任何降解便迅速随尿液排出。这些结果表明,由GF2、GF3和GF4组成的低聚果糖几乎不被胃肠道和内脏器官的消化酶水解,这向我们表明低聚果糖在体内不作为能量来源被利用。