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showed that TMAO not only promoted cellular inflammation but also accounted for oxidative stress, thus playing an indirect role in promoting expression of inflammatory cytokines ( In human umbilical vein endothelial cells (HUVECs) and aortas from ApoE -/- mice, TMAO increased the concentrations of reactive oxygen species (ROS), especially superoxide, by inhibiting the SIRT3-SOD2-mitochondrial ROS signaling pathway ( Endothelial dysfunction and thrombosis TMAO may lead to endothelial dysfunction

Based on the research question posed, 24 search criteria were developed as listed in Supplementary Materials Appendix A

Among these benefits, recovery and repair stand out as some of the most commonly studied outcomes

Identification of cardiac oxidoreductase(s) involved in the metabolism of the lipid peroxidation-derived aldehyde-4-hydroxynonenal

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