In the previous report it was observed that large amount of maltitol caused diarrhoea in mammalian system, and maltitol was not digested in vitro significantly by gastrointestinal tract. It has been considered that maltitol is not absorbed in mammalian digestive tract. In this report, absorption and excretion of maltitol-U-14C were observed with rat in vitro and in vivo.
In the experiment of intestinal everted sac, maltitol-U-
14C was slightly transported, and the rate of transport was as jejunum, ileum and duodenum in order. However, the maltitol-U-
14C concentration in serosa of the normal jejunum, where relative amount of maltitol-U-
14C seemed to be transported, was approximately one-tenth of that in mucosa after incubation for 60 min. at 37°C. When rats were adapted to maltitol, they showed a tendency to decrease the maltitol absorption.
On the observation of maltitol-U-
14C orally administered, over 60% of them was remained in gastro-intestinal tract, and only 8% of radioactivities (ca. 8%) was detected in the except for gastrointestinal tract. Relative amount of absorbed radioactivities (ca 5%) were excreted in the urine 24 hours after the administration, and a part of them (1.2%) were expired as respiratory
14CO
2.
On the observation of maltitol-U-
14C intravenously administered, about 35% of them were excreted in the urine within one hour after the injection, over 60% were 3 hours and over 85% were 24 hours after the administration.
When the rat was adapted to maltitol, passage of maltitol-U-
14C through gastrointestinal tract from duodenum to caecum was elevated, and the excretion of absorbed maltitol-U-
14C into urine had also tendency to increase. However, conversion of maltitol-U-
14C to respiratory
14CO
2 did not change in the maltitol adaptation.
From these results, it is confirmed that maltitol was slightly absorbed from intestine, and that absorbed maltitol was relatively quickly excreted in urine. Maltitol was considered to be utilized a little in mammalian tissues.
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