Zinc decreases C-reactive protein, lipid peroxidation, and inflammatory cytokines in elderly subjects: a potential implication of zinc as an atheroprotective agent

被引:294
作者
Bao, Bin [1 ]
Prasad, Ananda S. [1 ]
Beck, Frances W. J. [1 ]
Fitzgerald, James T. [2 ]
Snell, Diane [1 ]
Bao, Ginny W. [1 ]
Singh, Tapinder [1 ]
Cardozo, Lavoisier J.
机构
[1] Wayne State Univ, Sch Med, Dept Internal Med, Detroit, MI 48201 USA
[2] Univ Michigan, Sch Med, Ann Arbor, MI USA
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; PROLIFERATOR-ACTIVATED RECEPTOR; CORONARY-ARTERY-DISEASE; CARDIOVASCULAR-DISEASE; TRANSCRIPTION FACTORS; ENDOTHELIAL-CELLS; ANGIOTENSIN-II; INCREASED RISK; NITRIC-OXIDE; DEFICIENCY;
D O I
10.3945/ajcn.2009.28836
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Chronic inflammation and oxidative stress are common risk factors for atherosclerosis. Zinc is an essential micronutrient that can function as an antiinflammatory and antioxidative agent, and as such, it may have atheroprotective properties. Objective: We hypothesized that zinc down-regulates the production of atherosclerosis-related cytokines/molecules in humans. Design: To examine these effects, we conducted a randomized, double-blinded, placebo trial of zinc supplementation in elderly subjects. We recruited 40 healthy elderly subjects (aged 56-83 y) and randomly assigned them to 2 groups. One group was given an oral dose of 45 mg zinc/d as a gluconate for 6 mo. The other group was given a placebo. Cell culture models were conducted to study the mechanism of zinc as an atheroprotective agent. Results: After 6 mo of supplementation, the intake of zinc, compared with intake of placebo, increased the concentrations of plasma zinc and decreased the concentrations of plasma high-sensitivity C-reactive protein (hsCRP), interleukin (IL)-6, macrophage chemoattractant protein 1 (MCP-1), vascular cell adhesion molecule 1 (VCAM-I), secretory phospholipase A2, and malondialdehyde and hydroxyalkenals (MDA+HAE) in elderly subjects. Regression analysis showed that changes in concentrations of plasma zinc were inversely associated with changes in concentrations of plasma hsCRP, MCP-1, VCAM-1, and MDA+HAE after 6 mo of supplementation. In cell culture studies, we showed that zinc decreased the generation of tumor necrosis factor-alpha, IL-1 beta, VCAM-1, and MDA+HAE and the activation of nuclear transcription factor kappa B and increased antiinflammatory proteins A20 and peroxisome proliferator activated receptor-alpha in human monocytic leukemia THP-1 cells and human aortic endothelial cells compared with zinc-deficient cells. Conclusion: These findings suggest that zinc may have a protective effect in atherosclerosis because of its antiinflammatory and antioxidant functions. Am J Clin Nutr 2010;91:1634-41.
引用
收藏
页码:1634 / 1641
页数:8
相关论文
共 35 条
[2]   Increasing levels of interleukin (IL)-1Ra and IL-6 during the first 2 days of hospitalization in unstable angina are associated with increased risk of in-hospital coronary events [J].
Biasucci, LM ;
Liuzzo, G ;
Fantuzzi, G ;
Caligiuri, G ;
Rebuzzi, AG ;
Ginnetti, F ;
Dinarello, CA ;
Maseri, A .
CIRCULATION, 1999, 99 (16) :2079-2084
[3]   Obesity, peroxisome proliferator-activated receptor, and atherosclerosis in type 2 diabetes [J].
Blaschke, F ;
Takata, Y ;
Caglayan, E ;
Law, RE ;
Hsueh, WA .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (01) :28-40
[4]   PRACTICAL RECOMMENDATIONS AND NEW THERAPIES FOR WILSONS-DISEASE [J].
BREWER, GJ .
DRUGS, 1995, 50 (02) :240-249
[5]  
Clemons TE, 2004, ARCH OPHTHALMOL-CHIC, V122, P716, DOI 10.1001/archopht.122.5.716
[6]   NF-κB:: pivotal mediator or innocent bystander in atherogenesis? [J].
Collins, T ;
Cybulsky, MI .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (03) :255-264
[7]   Zinc attenuates tumor necrosis factor-mediated activation of transcription factors in endothelial cells [J].
Connell, P ;
Young, VM ;
Toborek, M ;
Cohen, DA ;
Barve, S ;
McClain, CJ ;
Hennig, B .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 1997, 16 (05) :411-417
[8]  
Luz Protásio Lemos da, 2005, Clinics, V60, P415
[9]   Peroxisome proliferator-activated receptor α negatively regulates the vascular inflammatory gene response by negative cross-talk with transcription factors NF-κB and AP-1 [J].
Delerive, P ;
De Bosscher, K ;
Besnard, S ;
Vanden Berghe, W ;
Peters, JM ;
Gonzalez, FJ ;
Fruchart, JC ;
Tedgui, A ;
Haegeman, G ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32048-32054
[10]  
Futterman L G, 1998, Am J Crit Care, V7, P240