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Food & Nutrition Science

Isomaltodextrin, a highly branched α-glucan, increases rat colonic H2 production as well as indigestible dextrin

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Pages 554-563 | Received 05 Aug 2015, Accepted 28 Sep 2015, Published online: 03 Dec 2015

Figures & data

Table 1. Food intake, bodyweight gain, breath and flatus H2 excretion, portal and abdominal H2 concentrations in rats fed nondigestible α-glucan for 14 days (Expt. 1).

Fig. 1. Change in (breath + flatus) H2 excretion in rats fed the (C), IMD, ID and HAS diets for 14 days (Expt. 1).

Notes: Values are means, with their standard errors represented by vertical bars, n = 8. Labeled means at a specific time point without a common letter differ, p < 0.05. Repeated-measures 2-way ANOVA was used to analyze H2 excretion among the three high-fat groups across time (NDS, p < 0.0001; time, p < 0.0001; interaction, p = 0.0052). (C), th group fed the control diet; HAS, group fed the high amylose cornstarch diet (104 g/kg); H2, hydrogen; ID, group fed the 8.8% indigestible dextrin diet; IMD, groups fed the 16.7% isomaltodextrin diet.
Fig. 1. Change in (breath + flatus) H2 excretion in rats fed the (C), IMD, ID and HAS diets for 14 days (Expt. 1).

Table 2. Weight of cecal tissue and content, cecal organic acid concentration, and bacterial enzyme activity, counts and ratio in rats fed nondigestible α-glucan for 14 days (Expt. 1).

Table 3. Dose response of isomaltodextrin on food intake, bodyweight gain, breath and flatus H2 excretion, portal and abdominal H2 concentrations in rats.

Fig. 2. Dose response of IMD on (breath + flatus) H2 excretion in rats (Expt. 2).

Notes: Values are means, with their standard errors represented by vertical bars, n = 8. Labeled means at a specific time point without a common letter differ, p < 0.05. Repeated-measures 2-way ANOVA was used to analyze H2 excretion among the three high-fat groups across time (dose, p < 0.0001; time, p < 0.0001; interaction, p < 0.0001). C, th group fed the control diet; H2, hydrogen; 3.3IMD-16.7IMD, groups fed the 3.3–16.7% isomaltodextrin diet.
Fig. 2. Dose response of IMD on (breath + flatus) H2 excretion in rats (Expt. 2).

Table 4. Dose response of isomaltodextrin on weight of cecal tissue and content, cecal organic acid concentration, and bacterial enzyme activity, counts and ratio in rats.

Table 5. Comparison between isomaltodextrin and fructooligosaccharide on food intake, bodyweight gain, breath and flatus H2 excretion, portal and abdominal H2 concentrations in rats.

Fig. 3. Comparison between IMD and FOS on (breath + flatus) H2 excretion in rats (Expt. 3).

Notes: Values are means, with their standard errors represented by vertical bars, n = 8. Labeled means at a specific time point without a common letter differ, p < 0.05. Repeated-measures 2-way ANOVA was used to analyze H2 excretion among the three high fat groups across time (NDF, p < 0.0001; time, p < 0.0001; interaction, p < 0.0046). C, th group fed the control diet; FOS, groups fed the 5.2% fructooligosaccharide diet; H2, hydrogen; IMD, groups fed the 16.7% isomaltodextrin diet.
Fig. 3. Comparison between IMD and FOS on (breath + flatus) H2 excretion in rats (Expt. 3).

Table 6. Comparison between isomaltodextrin and fructooligosaccharide on weight of cecal tissue and content, cecal organic acid concentration, and bacterial enzyme activity, counts and ratio in rats.

Supplemental material

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