4.6 Article

Effect of a diet rich in galactose or fructose, with or without fructooligosaccharides, on gut microbiota composition in rats

期刊

FRONTIERS IN NUTRITION
卷 9, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnut.2022.922336

关键词

fructose; galactose; fructooligosaccharides; gut microbiota; 16S rRNA

资金

  1. FORMAS
  2. ERA-NET of the EU Horizon 2020 Research and Innovation Programme
  3. Swedish Research Council [727565]
  4. Swedish Research Council (Formas ) [2017-05840]
  5. Chalmers Foundation [2016-003114]
  6. Ministry of Higher Education Malaysia
  7. Universiti Malaysia Pahang
  8. Swedish Research Council [2017-05840] Funding Source: Swedish Research Council

向作者/读者索取更多资源

Recent studies have found that a diet high in sugars can affect the gut microbiota, but there is a lack of experimental evidence. This study investigated the effects of high fructose or galactose intake, with or without fructooligosaccharides (FOS), on gut microbiota composition in rats. The results showed that the intake of fructose or galactose did not have a coherent effect on gut microbiota composition, but the addition of FOS increased Bifidobacterium. However, gut microbiota composition was associated with metabolic factors and gut permeability markers, which warrant further investigations.
Recent studies suggest that a diet rich in sugars significantly affects the gut microbiota. Adverse metabolic effects of sugars may partly be mediated by alterations of gut microbiota and gut health parameters, but experimental evidence is lacking. Therefore, we investigated the effects of high intake of fructose or galactose, with/without fructooligosaccharides (FOS), on gut microbiota composition in rats and explored the association between gut microbiota and low-grade systemic inflammation. Sprague-Dawley rats (n = 6/group) were fed the following isocaloric diets for 12 weeks (% of the dry weight of the sugars or FOS): (1) starch (control), (2) fructose (50%), (3) galactose (50%), (4) starch+FOS (15%) (FOS control), (5) fructose (50%)+FOS (15%), (6) galactose (50%)+FOS (15%), and (7) starch+olive (negative control). Microbiota composition in the large intestinal content was determined by sequencing amplicons from the 16S rRNA gene; 341F and 805R primers were used to generate amplicons from the V3 and V4 regions. Actinobacteria, Verrucomicrobia, Tenericutes, and Cyanobacteria composition differed between diets. Bifidobacterium was significantly higher in all diet groups where FOS was included. Modest associations between gut microbiota and metabolic factors as well as with gut permeability markers were observed, but no associations between gut microbiota and inflammation markers were observed. We found no coherent effect of galactose or fructose on gut microbiota composition. Added FOS increased Bifidobacterium but did not mitigate potential adverse metabolic effects induced by the sugars. However, gut microbiota composition was associated with several metabolic factors and gut permeability markers which warrant further investigations.

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