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Dietary fat intake and age influence gut microbiota and colonic inflammation in C57BL/6J mice

Authors
Kim, Su JeongSung, Mi-KyungPark, Mi-YoungKim, Sun-Eun
Issue Date
Apr-2015
Publisher
FEDERATION AMER SOC EXP BIOL
Citation
FASEB JOURNAL, v.29, no.S1, pp 601.5 - 601.5
Journal Title
FASEB JOURNAL
Volume
29
Number
S1
Start Page
601.5
End Page
601.5
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/5529
DOI
10.1096/fasebj.29.1_supplement.601.5
ISSN
0892-6638
1530-6860
Abstract
Recent studies have showed that diet-induced alterations of gut microbiota composition play a pivotal role in the development of metabolic diseases. We investigated whether dietary fat and age would affect gut microbiota, permeability and inflammation. C57BL/6J mice were randomly assigned to either normal fat diet (ND) or high-fat diet (HD) group. After 10 wks, a half of mice in each group were switched to either HD or ND feeding for additional 10 wks. Microbiome composition and diversity were analyzed by 16S rRNA-based pyrosequencing. Colonic mRNA expressions of tight junction (TJ) proteins and inflammatory cytokines were measured by qPCR. DNA strand break was determined using comet assay. The main bacterial phyla of mice were Frimicutes, Bacteroidetes, and Actinobacteria. Diversity of gut microbiota was reduced in mice fed HD compared to those of mice fed ND. In mice fed HD for 20 wks, the proportions of Actinobacteria and Firmicutes increased while the proportion of Bacteroidetes decreased compared to mice fed ND for 20wks. The proportions of Firmicutes and Bacteroidetes were related with age while the proportion of Actinobacteria was related with dietary fat content. High-fat diet was negatively associated with the expressions of TJ proteins while it was positively associated with the expression of inflammatory cytokines. Changes in the expression of TJ protein and inflammatory cytokines followed changes in fat content of the diet. Our data showed that both dietary fat intake and age affect gut microbiota composition as well as colonic membrane integrity and inflammation.
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