
High-fat diet-induced colonocyte dysfunction escalates microbiota-derived trimethylamine N-oxide.
A Western-style, high-fat diet promotes cardiovascular disease, in part because it is rich in choline, which is converted to trimethylamine (TMA) by the gut microbiota. However, whether diet-induced changes in intestinal physiology can alter the metabolic capacity of the microbiota remains unknown. Using a mouse model of diet-induced obesity, we show that chronic exposure to a high-fat diet escalates Escherichia coli choline catabolism by altering intestinal epithelial physiology. A high-fat diet impaired the bioenergetics of mitochondria in the colonic epithelium to increase the luminal bioavailability of oxygen and nitrate, thereby intensifying respiration-dependent choline catabolism of E. coli In turn, E. coli choline catabolism increased levels of circulating trimethlamine N-oxide, which is a potentially harmful metabolite generated by gut microbiota.
Duke Scholars
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Related Subject Headings
- Oxygen Consumption
- Obesity
- Nitrates
- Mitochondria
- Mice, Inbred C57BL
- Mice
- Methylamines
- Male
- Intestinal Mucosa
- Inflammation
Citation

Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Oxygen Consumption
- Obesity
- Nitrates
- Mitochondria
- Mice, Inbred C57BL
- Mice
- Methylamines
- Male
- Intestinal Mucosa
- Inflammation