Suppressive Effects of Hydroxytyrosol on Oxidative Stress and Nuclear Factor-κB Activation in THP-1 Cells

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  • Zhang Xiaomei
    Department of Laboratory Medicine, College of Medicine, Dalian University Department of Toxicology, Dalian Medical University
  • Cao Jun
    Department of Toxicology, Dalian Medical University
  • Jiang Liping
    China-Japanese Joint Institute for Medical and Phamaceutical Science, Dalian Medical University
  • Zhong Laifu
    Department of Toxicology, Dalian Medical University

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  • Suppressive effects of hydroxytyrosol on oxidative stress and nuclear factor kB activation in THP 1 cells
  • Suppressive Effects of Hydroxytyrosol on Oxidative Stress and Nuclear Factor-κB Activation in THP-1 Cells

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Abstract

This study was designed to investigate whether hydroxytyrosol (HT) may ameliorate oxidative stress and nuclear factor kappaB (NF-κB) activation in the lipopolysaccharide (LPS)-stimulated THP-1 cell line. We measured the intracellular reactive oxygen species (ROS) formation using 2,7-dichlorofluorescein diacetate (DCFH-DA) as a fluorescent probe. Intracellular glutathione (GSH) level was estimated by fluorometric methods. Nitric oxide (NO) production was measured as nitrite (a stable metabolite of NO) concentrations using the Griess reagent system following Jiancheng Institute of Biotechnology protocols. To study the effect of HT on LPS-induced NF-κB activation in THP-1 cells, Western blot analysis of the nuclear fraction of cell lysates was performed. The results showed that treatment of THP-1 cells with HT significantly reduced LPS-stimulated NO production and ROS formation in a concentration-dependent manner. HT at 50 and 100 μM concentrations increased the GSH level. The specific DNA-binding activities of NF-κB on nuclear extracts from 50 and 100 μM HT treatments were significantly suppressed. The antioxidant N-acetylcysteine (NAC) also showed the same effects as HT on LPS-induced ROS and NO generation, change of GSH level, and NF-κB activation. These findings suggest that HT has antioxidant activity to suppress intracellular oxidative stress and NF-κB activation in THP-1 cells.

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