DETERMINATION OF SUGAR ALCOHOL AND POLYDEXTROSE(R) ABSORPTION IN HUMANS BY THE BREATH HYDROGEN (H2) TECHNIQUE - THE STOICHIOMETRY OF HYDROGEN-PRODUCTION AND THE INTERACTION BETWEEN CARBOHYDRATES ASSESSED INVIVO AND INVITRO
G. Livesey et al., DETERMINATION OF SUGAR ALCOHOL AND POLYDEXTROSE(R) ABSORPTION IN HUMANS BY THE BREATH HYDROGEN (H2) TECHNIQUE - THE STOICHIOMETRY OF HYDROGEN-PRODUCTION AND THE INTERACTION BETWEEN CARBOHYDRATES ASSESSED INVIVO AND INVITRO, European journal of clinical nutrition, 47(6), 1993, pp. 419-430
The production of hydrogen from substrates and substrate mixture of su
gar alcohols and Polydextrose(R) was determined, both in vivo using th
e breath hydrogen test, and in vitro, using human faecal microorganism
s in anaerobic culture. One objective was to test a previous assumptio
n that the stoichiometry of hydrogen production from different alterna
tive carbohydrates is similar. Another objective was to discover wheth
er hydrogen responses from mixtures of substrates were simply additive
, or whether interactions occurred. The breath tests were performed in
a 10 subject X 10 substrate factorial design with substrates and subs
trate mixtures (5-11 g) administered in 42 g chocolate confectionery.
Incorporation of the alternative carbohydrates lactitol (L), Isomalt (
I) and Polydextrose(R) (P) into otherwise conventional confectionery i
ncreased breath hydrogen production by approximately 112, 73 and 11%/g
respectively. There was no interaction between L and I or between P a
nd I, but a combination of L and P approximately doubled the breath hy
drogen anticipated from their individual contributions (P < 0.05). Ana
erobic cultures showed a sixfold range in the efficiency of converting
individual substrates and mixtures to hydrogen gas (0.003-0.018 kJ H-
2 per kJ carbohydrate). The positive interaction between L and P, and
the lack of interaction between L and 1, and between P and I, found in
vivo were reproduced in vitro. The work showed that interpretation of
the hydrogen breath test is confounded by differing stoichiometries f
or hydrogen production, by interaction between substrates and by an un
certain extent to which small intestinal hydrolysis yielding species w
ith a fermentation stoichiometry that differs from the parent substrat
e.