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- W2338261812 abstract "FetuinA is associated with endothelial dysfunction, which is regulated by oxidative stress. We hypothesised that FetA through toll-like receptor 4 (TLR4) and ROS production induces vascular dysfunction. Mesenteric arteries and vascular cells from WKY rats were studied. Vascular function was analysed by wire myography in the presence or absence of FetA (50 ng/mL) and/or CLI095 (CLI – 10–6M – TLR4 inhibitor). WKY vessels exposed to FetA were less sensitive to acetylcholine (Ach)-induced and sodium nitroprusside (SNP)-induced relaxation, while sensitivity to phenylephrine was increased by FetA; an effect blocked by N-acetylcysteine (antioxidant) and ML171 (Nox1 inhibitor). Inhibition of TLR4 blocked FetA effects on endothelial-dependent relaxation and contraction, but not on endothelial-independent relaxation. FetA increased ROS production (1 fold), but decreased H2O2 intracellular levels (0.5 fold) in endothelial cells (EC) (p" @default.
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- W2338261812 date "2015-11-01" @default.
- W2338261812 modified "2023-09-27" @default.
- W2338261812 title "35 Fetuin-A and toll-like receptor 4 regulate vascular function: role of Nox1" @default.
- W2338261812 doi "https://doi.org/10.1136/heartjnl-2015-308734.35" @default.
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