Inhibition of the respiratory burst by resveratrol in human monocytes: Correlation with inhibition of PI3K signaling

被引:43
作者
Poolman, TM
Ng, LL
Farmer, PB
Manson, MM
机构
[1] Univ Leicester, Dept Cardiovasc Sci, Pharmacol & Therapeut Grp, Leicester Royal Infirm, Leicester LE2 7LX, Leics, England
[2] Univ Leicester, Canc Biomarkers & Prevent Grp, Bioctr, Leicester LE1 7RH, Leics, England
基金
英国医学研究理事会;
关键词
resveratrol; NADPH oxidase; U937; cells; phosphatidylinositol; 3-kinase; Akt; mitogen-activated protein kinase; protein kinase C; reactive oxygen species; peroxidase; free radicals;
D O I
10.1016/j.freeradbiomed.2005.02.036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
trans-Resveratrol (t-RVT) has been shown to have a wide range of anti-inflammatory properties, some of which have been suggested to contribute to the molecular explanation of the French Paradox, a possible reason for the low incidence of heart disease in France. The ability of t-RVT to inhibit the production of reactive oxygen species (ROS) from monocytes (differentiated U937) was investigated using isoluminol, luminol, lucigenin, and 2',7'-dichlorofluorescein (DCF). t-RVT (0.1-50 mu M) was found to significantly inhibit cellular ROS production stimulated by f-Met-Leu-Phe (fMLP), 12-phorbol 13-myristate, and arachidonic acid after a 1-h preincubation. The efficacy of t-RVT could be increased if it was added directly into the assay. NADPH-dependent superoxide production was measured in cell homogenates and t-RVT (10-50 mu M) was found to have no effect on this activity. The majority of these redox probes require a peroxidase to be oxidized; therefore, the inhibitory effect of t-RVT on ROS measured by these probes is complicated by its ability to be oxidized by peroxidase enzymes and thus compete with the probe. t-RVT, known to be oxidized by the horseradish peroxidase (HRP)/H2O2 system, was found to inhibit the HRP-dependent oxidation of the fluorescent probe DCF and the chemiluminescent probe isoluminol. However, using a redox probe that did not require oxidation by a peroxidase (lucigenin), significant inhibition was still observed. Moreover, the inhibitory effects of t-RVT on fMLP-induced ROS production correlated with significant inhibitory effects on fMLP-induced phosphatidylinositol 3-kinase (PI3K) activity at 50 mu M and Akt phosphorylation (10-50 mu M). Other known inhibitors of both PI3K and Akt were also found to inhibit this response. Therefore, inhibition of signaling through the PI3K to NADPH oxidase by t-RVT might represent an important anti-inflammatory mechanism. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:118 / 132
页数:15
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