Resveratrol and curcumin reduce the respiratory burst of Chlamydia-primed THP-1 cells

被引:46
作者
Deby-Dupont, G
Mouithys-Mickalad, A
Serteyn, D
Lamy, M
Deby, C
机构
[1] Univ Liege, Inst Chim, Ctr Oxygen Res & Dev, B-4000 Cointe Ougree, Belgium
[2] Univ Liege, Univ Hosp, Dept Anaesthesia & Intens Care, B-4000 Liege, Belgium
[3] Univ Liege, Fac Med Vet, Serv Anesthesie & Chirurgie Grands Animaux, B-4000 Liege, Belgium
关键词
THP-1; Chlamydia pneumoniae; resveratrol; curcumin; NADPH oxidase; priming; IL-8; TNF alpha;
D O I
10.1016/j.bbrc.2005.05.073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The intracellular bacterium Chlamydia pneumoniae is involved in the inflammation process of atherosclerosis. We previously demonstrated that C. pneumonia infected monocytes (THP-1 cells) responded to stimulation by an increased respiratory burst linked to an increased NADPH oxidase (NOX) activity. We now tested agents acting on the assembly of the NOX subunits or on protein kinase C, a trigger of NOX activity. Apocynin, resveratrol, rutin, quercetin, curcumin, and tocopherols were tested. The cells were pre-incubated with Chlamydia and the agent for 19 h, and then stimulated with phorbol myristate acetate. The NOX activity was monitored by measuring the hydrogen peroxide production. Resveratrol and curcumin (10(-4)-10(-6)M) were better inhibitors than apocynin. a-Tocopherol was inactive, and gamma-tocopherol inhibitor at 10(-4) M only. Quercetin was inactive, and rutin a moderate but significant inhibitor. The inhibition by resveratrol was increased by 10(-6) M rutin or quercetin. Resveratrol and curcumin thus appeared to be interesting for atherosclerosis treatment. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:21 / 27
页数:7
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