Molecular Inflammation as an Underlying Mechanism of the Aging Process and Age-related Diseases

被引:183
作者
Chung, H. Y. [1 ,2 ]
Lee, E. K. [1 ,2 ]
Choi, Y. J. [1 ,2 ]
Kim, J. M. [1 ,2 ]
Kim, D. H. [3 ]
Zou, Y. [4 ]
Kim, C. H. [5 ]
Lee, J. [1 ,2 ]
Kim, H. S. [1 ,2 ]
Kim, N. D. [1 ,2 ]
Jung, J. H. [1 ,2 ]
Yu, B. P. [6 ]
机构
[1] Pusan Natl Univ, Mol Inflammat Res Ctr Aging Intervent, Pusan 609735, South Korea
[2] Pusan Natl Univ, Coll Pharm, Dept Pharm, Pusan 609735, South Korea
[3] Univ Pittsburgh, Childrens Hosp Pittsburgh, Dept Pediat, Sch Med,Rangos Res Ctr, Pittsburgh, PA 15224 USA
[4] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[5] Theragen Bio Inst AICT, Div Genome Anal, Suwon 443270, South Korea
[6] Univ Texas Hlth Sci Ctr San Antonio, Dept Physiol, San Antonio, TX 78229 USA
关键词
inflammation; oxidative stress; cytokines; gingivitis; aging; age-related diseases; NF-KAPPA-B; NECROSIS-FACTOR-ALPHA; FORKHEAD TRANSCRIPTION FACTORS; ACTIVATED RECEPTORS PPARS; CALORIE RESTRICTION; OXIDATIVE STRESS; GENE-EXPRESSION; INSULIN-RESISTANCE; REACTIVE OXYGEN; PERIODONTAL INFLAMMATION;
D O I
10.1177/0022034510387794
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aging is a biological process characterized by time-dependent functional declines that are influenced by changes in redox status and by oxidative stress-induced inflammatory reactions. An organism's pro-inflammatory status may underlie the aging process and age-related diseases. In this review, we explore the molecular basis of low-grade, unresolved, subclinical inflammation as a major risk factor for exacerbating the aging process and age-related diseases. We focus on the redox-sensitive transcription factors, NF-kappa B and FOXO, which play essential roles in the expression of pro-inflammatory mediators and anti-oxidant enzymes, respectively. Major players in molecular inflammation are discussed with respect to the age-related up-regulation of pro-inflammatory cytokines and adhesion molecules, cyclooxygenase-2, lipoxygenase, and inducible nitric oxide synthase. The molecular inflammation hypothesis proposed by our laboratory is briefly described to give further molecular insights into the intricate interplay among redox balance, pro-inflammatory gene activation, and chronic age-related inflammatory diseases. The final section discusses calorie restriction as an aging-retarding intervention that also exhibits extraordinarily effective anti-inflammatory activity by modulating GSH redox, NF-kappa B, SIRT1, PPARs, and FOXOs.
引用
收藏
页码:830 / 840
页数:11
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