alpha-Tocopherol modulates human umbilical vein endothelial cell expression of Cu/Zn superoxide dismutase and catalase and lipid peroxidation

作者：Nakamura Yukiko K; Omaye Stanley T^*

来源：Nutrition Research, 2008, 28(10): 671-680.

DOI：10.1016/j.nutres.2008.07.002

• alpha-Tocopherol
• Human
• Endothelial cells
• PPAR gamma
• NF-kappa B
• Lipid peroxidation
• SOD
• Catalase

Recent studies suggest the potential of alpha-tocopherol as a gene regulator, possibly through peroxisome proliferator-activated receptor gamma (PPAR gamma) activation due to the structural similarity of alpha-tocopherol to a PPAR gamma ligand, troglitazone. Other investigators have suggested that a link exists between induction of the antioxidant enzymes Cu/Zn superoxide dismutase (SOD) and catalase and PPAR gamma activation. This study was designed to examine whether alpha-tocopherol modulates expression of Cu/Zn SOD anti catalase in human umbilical vein endothelial cells through redox-sensitive transcription factors, PPAR gamma, and nuclear factor-kappa B (NF-kappa B). alpha-Tocopherol treatments showed significant increases in both PPAR gamma (1.4- to 2.2-fold, P <.01) and NF-kappa B p50 (1.3- to 1.5-fold, P <.005) DNA binding activities compared with vehicle control. Significant increases in Cu/Zn SOD mRNA levels (6.0-fold, P <.005) and catalase rnRNA (8.0-fold, P <.005) and its protein levels (2.3-fold, P <.005) and lipid peroxidation levels (5.3-fold, P <.005) were observed at the lowest concentration (10 mu mol/L) of alpha-tocopherol treatments. Both mRNA and protein levels of these 2 antioxidant enzymes were positively associated with lipid peroxidation (P <.05). alpha-Tocopherol may play a role not only in preventing against oxidative damage as an exogenous antioxidant by scavenging free radicals and superoxide but also in modulating the expression of the endogenous antioxidant enzymes as a gene regulator through PPAR gamma and NF-kappa B in the vascular cells. The alpha-tocopherol-mediated gene expression is either stimulatory or inhibitory, depending on its oxidative status or its concentrations.

• 出版日期2008-10