Key result
Polymethoxyflavones suppress bacterial lyases and reduce hepatic TMAO formation by inhibiting FMO3 expression.
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Demonstrates that orange peel polymethoxyflavones inhibit enzymes producing TMA and TMAO, suggesting dietary strategies to mitigate cardiovascular disease risk.
This study investigates the inhibitory effects of polymethoxyflavones (PMFs) on enzymes involved in the production of trimethylamine (TMA) and trimethylamine-N-oxide (TMAO). PMFs were isolated from Valencia orange peel and identified using column separation and NMR techniques. The findings reveal that nobiletin and 3,6,7,8,2',5'-hexamethoxyflavone significantly suppress cntA/B and cutC/D, respectively. Furthermore, 3,6,7,8,2',5'-hexamethoxyflavone decreases the level of TMAO formation by suppressing the FMO3 mRNA level. This study elucidates that specific structural features of PMFs can contribute to their interactions with enzymes. Our study represents the first demonstration of the ability of PMFs to mitigate the risk of cardiovascular disease (CVD) by inhibiting enzymes responsible for TMA production, which are generated by gut microbiomes. Furthermore, we introduce a novel model system utilizing TMA-induced HepG2 cells to assess and compare the inhibitory effects of PMFs on TMAO production. These findings could pave the way for the development of novel therapeutic approaches to manage CVD.
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Lee et al. (2023) studied Cardiovascular disease risk (TMA and TMAO production). Polymethoxyflavones (nobiletin and 3,6,7,8,2',5'-hexamethoxyflavone) from Valencia orange peel was evaluated on Inhibition of cntA/B and cutC/D enzymes and TMAO formation via FMO3 mRNA suppression. Polymethoxyflavones (nobiletin and 3,6,7,8,2',5'-hexamethoxyflavone) significantly suppressed cntA/B and cutC/D enzymes and decreased TMAO formation by suppressing FMO3 mRNA in HepG2 cells.
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