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Ameliorative effects of konjac glucomannan on human faecal β-glucuronidase activity, secondary bile acid levels and faecal water toxicity towards Caco-2 cells.

The British journal of nutrition
February 1, 2011
Wen-Tzu Wu et al. (3 authors)
Journal ArticleRandomized Controlled TrialResearch Support, Non-U.S. Gov'tHuman StudyAnimal StudyClinical
Study Details

Study Goal

The researchers aimed to assess the effects of a konjac glucomannan (KGM) supplement on precancerous markers of colon cancer in a low-fibre diet.

Results Summary

The KGM supplement significantly reduced faecal β-glucuronidase activity and secondary bile acid levels, increased survival rates of Caco-2 cells, and reduced DNA damage. It also improved faecal microbial ecology by increasing bifidobacteria and lactobacilli levels.

Population

Adult volunteers

Effective Dosage

4.5 g/d

Duration

4 weeks

Interactions

None mentioned

Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Konjac glucomannan (KGM)
increase
human colon microbial ecology
mice
-
has been shown to increase
#1
Konjac glucomannan (KGM)
decrease
faecal toxicity
mice
-
has been shown to reduce
#2
KGM supplement
decrease
faecal β-glucuronidase activity
Adult volunteers
25·6 (se 7·8) %
significantly decreased
#3
KGM supplement
decrease
faecal secondary bile acid level
Adult volunteers
42·4 (se 11·8) %
significantly decreased
#4
defined diet supplemented with placebo
no change
these determinants
Adult volunteers
-
did not improve
#5
KGM-supplemented diet
increase
the survival rate (%) of Caco-2 cells co-incubated with faecal water for 1 and 3 h
-
-
significantly increased
#6
KGM
decrease
the DNA damage induced by the faecal water alone or in combination with H2O2
-
-
significantly reduced
#7
KGM-supplemented diet
increase
faecal bifidobacteria and lactobacilli levels
Adult volunteers
-
increased
#8
supplementation of KGM into a low-fibre diet
increase
the faecal microbial ecology and metabolites
-
-
improved
#9
supplementation of KGM into a low-fibre diet
decrease
toxicity of faecal water and precancerous risk factors of human colon cancer
-
-
may contribute to the reduced
#10
Abstract

Konjac glucomannan (KGM) has been shown to increase human colon microbial ecology and reduce faecal toxicity in mice. The main goal of the present study was to assess the effects of a KGM supplement into a low-fibre diet on precancerous markers of colon cancer in a double-blind, placebo- and diet-controlled study. Adult volunteers consumed defined diets supplemented with konjac (4·5 g/d) or placebo (maize starch) for 4 weeks. Stools collected before and at the end of the supplementation were analysed for β-glucosidase, β-galactosidase and β-glucuronidase activities, microflora and bile acids. Faecal water was co-incubated with Caco-2 cells, a model of human colonocytes, to determine the cytotoxicity and DNA-damaging effect as assessed by the comet assay. The results indicated that the KGM supplement significantly decreased faecal β-glucuronidase activity by 25·6 (se 7·8) % and faecal secondary bile acid level by 42·4 (se 11·8) %. In contrast, consuming the defined diet supplemented with placebo for 4 weeks did not improve these determinants. The KGM-supplemented diet, but not the placebo diet, significantly increased the survival rate (%) of Caco-2 cells co-incubated with faecal water for 1 and 3 h, respectively. In addition, KGM significantly reduced the DNA damage induced by the faecal water alone or in combination with H2O2. The faecal bifidobacteria and lactobacilli levels increased only with the KGM-supplemented diet. Therefore, we conclude that supplementation of KGM into a low-fibre diet improved the faecal microbial ecology and metabolites, which may contribute to the reduced toxicity of faecal water and precancerous risk factors of human colon cancer.

Medical Subject Headings (MeSH)
AdultBile Acids and SaltsCaco-2 CellsDNA DamageFecesFemaleGlucuronidaseHumansMaleMannansMiddle AgedPlacebosWaterZea mays
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality90/10
Citation Metrics
Total Citations27
Citations/Year1.9
Relative Citation Ratio0.88
NIH Percentile45.3%
Research Impact Scores
APT Score0.25
Weight Score1.47
Normalized Score0.72
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