2018
DOI: 10.1038/s41430-018-0306-8
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Importance of gut microbiota in obesity

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Cited by 107 publications
(93 citation statements)
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“…and metabolic (Fig. 2) gene enrichment together is also in agreement with the well-established relationship between intestinal bacteria and metabolism in diverse species including fly [25][26][27][28]. As TAG levels were found altered in several of the above metabolic studies [11, [13][14][15][16][17], are associated with cold tolerance in D. melanogaster [13], and, notably, show alterations in the offspring of cold-exposed mice [9], we identified altered TAG regulation as a potential trait that might be inherited following cold exposure.…”
Section: Metabolic Alterationssupporting
confidence: 85%
“…and metabolic (Fig. 2) gene enrichment together is also in agreement with the well-established relationship between intestinal bacteria and metabolism in diverse species including fly [25][26][27][28]. As TAG levels were found altered in several of the above metabolic studies [11, [13][14][15][16][17], are associated with cold tolerance in D. melanogaster [13], and, notably, show alterations in the offspring of cold-exposed mice [9], we identified altered TAG regulation as a potential trait that might be inherited following cold exposure.…”
Section: Metabolic Alterationssupporting
confidence: 85%
“…Other than the BA receptors, intestinal microbiota may also play a role in the association of BA with obesity as they metabolize BA, which reciprocally affects their composition and abundance 5 . Gut microbiota composition has been closely linked to obesity and other metabolic alterations 93 . The resistance to HFD in FXR‐deficient mice is also transferable by microbiota transplantation 88 .…”
Section: Discussionmentioning
confidence: 99%
“…FXR activation by bile acids initiates a negative feedback pathway, such that bile acid synthesis is inhibited when FXR is activated. Intestinal microbiota are capable of producing secondary bile acids from ∼5 to 10% of hepatic-derived bile acids that affect host physiology by serving as FXR agonists, thus resulting in a smaller bile acid pool due to the inhibition of primary bile acid synthesis (692,693). Subjects with obesity and/or T2DM have been shown to have fewer plasma secondary bile acids in comparison to healthy control subjects (694), an effect that may reflect the altered gut microbial composition observed in obesity.…”
Section: Bile Acid Metabolismmentioning
confidence: 99%