Ch. Lifschitz et al., IN-VIVO STUDY OF COLONIC FERMENTATION OF CARBOHYDRATE IN INFANTS, Journal of pediatric gastroenterology and nutrition, 20(1), 1995, pp. 59-64
Dietary carbohydrate in the colon is fermented and converted into shor
t-chain fatty acids. We studied the fate of carbohydrate that arrives
in the colon under circumstances similar to those that occur during an
episode of diarrhea and determined whether a quantitative correlation
exists among certain indicators of colonic fermentation of carbohydra
te arriving in the large bowel. A stable-isotope method was used to es
timate carbon scavenging by the colon. Fourteen infants with severe ma
lnutrition and history of watery stools and/or increased numbers of st
ools in the preceding 20 days were studied. Infants underwent nasoceca
l intubation and a 60-min infusion of 0.5 g/kg glucose containing 5 mg
/kg of C-13-glucose. Stools were assessed for carbohydrate-fermenting
bacteria, acetate, glucose, and C-13 abundance; blood was assessed for
acetate; and breath was assessed for hydrogen. Some of the infants el
iminated the infusate per anus within 30 min of the infusion (group I;
n = 5), while others did so 120 min or more after the infusion (Group
II; n = 9). The volume of fecal output after the intracecal infusion
differed significantly between group I and group II (57 +/- 13 vs. 24
+/- 4 ml; p < 0.05). Although baseline breath hydrogen (3 +/- 1 vs. 10
+/- 4 parts per million) and plasma acetate (41 +/- 4 vs. 47 +/- 9 mu
M) values were not significantly different between groups, breath hyd
rogen values at 45 min after start of infusion were significantly lowe
r in group I than in group II (3 +/- 1 vs. 19 +/- 5 ppm; p = 0.008); 6
0 min after start of infusion, plasma acetate levels were significantl
y lower in group I than in group II (34 +/- 8 vs. 69 +/- 11 mu M; p =
0.02), and the difference remained significant throughout the study. R
egression analyses indicated a significant association between time el
apsed from start of intracolonic infusion and plasma acetate (p = 0.01
4) and breath hydrogen (p = 0.04) levels for group II. Although we fou
nd good correlation between two indicators of colonic fermentation, bl
ood acetate and breath hydrogen, these values did not correlate well w
ith carbon scavenging or fecal bacterial counts. It is possible that t
he way the colon handles the infusate-i.e., water absorption and/or se
cretion-may affect carbohydrate fermentation.