Atherosclerosis is characterized by endothelial dysfunction, mainly induced by inflammation and oxidative stress. Increased\nreactive oxygen species (ROS) production together with increased adhesion molecules and thrombogenic tissue factor (TF)\nexpression on endothelial cells has a key role in proatherogenic mechanisms. Therefore downmodulation of these molecules could\nbe useful for reducing the severity of inflammation and atherosclerosis progression. Dehydrozingerone (DHZ) is a nutraceutical\ncompound with anti-inflammatory and antioxidant activities. In this studywe evaluated the ability ofDHZ and its symmetric dimer\nto modulate hydrogen peroxide- (H2O2-) induced ROS production in human umbilical vein endothelial cells (HUVEC). We also\nevaluated intercellular adhesionmolecule- (ICAM-) 1, vascular cell adhesionmolecule- (VCAM-) 1, and TF expression in HUVEC\nactivated by tumor necrosis factor- (TNF-)
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