Flavin-containing monooxygenase 3 as a potential player in diabetes-associated atherosclerosis

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Author
Manthena, Praveen V.
Graham, Mark J.
Crooke, Rosanne M.
Esquejo, Ryan M.
Clish, Clary B.
Torrecilla, Esther
Vázquez, Gumersindo Fernández
Rubio, Miguel A.
Cabrerizo, Lucio
Barabash, Ana
Pernaute, Andrés Sánchez
Torres, Antonio J.
Vicent, David
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https://doi.org/10.1038/ncomms7498Metadata
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Miao, J., A. V. Ling, P. V. Manthena, M. E. Gearing, M. J. Graham, R. M. Crooke, K. J. Croce, et al. 2015. “Flavin-containing monooxygenase 3 as a potential player in diabetes-associated atherosclerosis.” Nature Communications 6 (1): 6498. doi:10.1038/ncomms7498. http://dx.doi.org/10.1038/ncomms7498.Abstract
Despite the well-documented association between insulin resistance and cardiovascular disease, the key targets of insulin relevant to the development of cardiovascular disease are not known. Here, using non-biased profiling methods, we identify the enzyme flavin-containing monooxygenase 3 (Fmo3) to be a target of insulin. FMO3 produces trimethylamine N-oxide (TMAO), which has recently been suggested to promote atherosclerosis in mice and humans. We show that FMO3 is suppressed by insulin in vitro, increased in obese/insulin resistant male mice and increased in obese/insulin-resistant humans. Knockdown of FMO3 in insulin-resistant mice suppresses FoxO1, a central node for metabolic control, and entirely prevents the development of hyperglycaemia, hyperlipidemia and atherosclerosis. Taken together, these data indicate that FMO3 is required for FoxO1 expression and the development of metabolic dysfunction.Other Sources
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391288/pdf/Terms of Use
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