Oxidative stress and vascular inflammation in aging

被引:470
作者
El Assar, Mariam [1 ]
Angulo, Javier [2 ]
Rodriguez-Manas, Leocadio [1 ,3 ]
机构
[1] Hosp Univ Getafe, Fdn Invest Biomed, Getafe, Spain
[2] Hosp Univ Ramon y Cajal, Inst Ramon y Cajal Invest Sanitaria, Madrid, Spain
[3] Hosp Univ Getafe, Serv Geriatr, Getafe, Spain
关键词
Arterial aging; Endothelial dysfunction; Nitric oxide; Oxidative stress; Reactive oxygen species; Inflammation; Nuclear factor-kappa B; Sirtuins; NF-KAPPA-B; NITRIC-OXIDE SYNTHASE; SMOOTH-MUSCLE-CELLS; EXTRACELLULAR-SUPEROXIDE DISMUTASE; ENDOTHELIAL PROGENITOR CELLS; RENIN-ANGIOTENSIN SYSTEM; HYDROGEN-PEROXIDE PRODUCTION; HYPOXIA-INDUCIBLE FACTORS; INDUCED NOX4 EXPRESSION; NECROSIS-FACTOR-ALPHA;
D O I
10.1016/j.freeradbiomed.2013.07.003
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
Vascular aging, a determinant factor for cardiovascular disease and health status in the elderly, is now viewed as a modifiable risk factor. Impaired endothelial vasodilation is a early hallmark of arterial aging that precedes the clinical manifestations of vascular dysfunction, the first step to cardiovascular disease and influencing vascular outcomes in the elderly. Accordingly, the preservation of endothelial function is thought to be an essential determinant of healthy aging. With special attention on the effects of aging on the endothelial function, this review is focused on the two main mechanisms of aging-related endothelial dysfunction: oxidative stress and inflammation. Aging vasculature generates an excess of the reactive oxygen species (ROS), superoxide and hydrogen peroxide, that compromise the vasodilatory activity of nitric oxide (NO) and facilitate the formation of the deleterious radical, peroxynitrite. Main sources of ROS are mitochondrial respiratory chain and NADPH oxidases, although NOS uncoupling could also account for ROS generation. In addition, reduced antioxidant response mediated by erythroid-2-related factor-2 (Nrf2) and downregulation of mitochondrial manganese superoxide dismutase (SOD2) contributes to the establishment of chronic oxidative stress in aged vessels. This is accompanied by a chronic low-grade inflammatory phenotype that participates in defective endothelial vasodilation. The redox-sensitive transcription factor, nuclear factor-kappa B (NF-kappa B), is upregulated in vascular cells from old subjects and drives a proinflammatory shift that feedbacks oxidative stress. This chronic NF-kappa B activation is contributed by increased angiotensin-II signaling and downregulated sirtuins and precludes adequate cellular response to acute ROS generation. Interventions targeted to recover endogenous antioxidant capacity and cellular stress response rather than exogenous antioxidants could reverse oxidative stress inflammation vicious cycle in vascular aging. Lifestyle attitudes such as caloric restriction and exercise training appear as effective ways to overcome defective antioxidant response and inflammation, favoring successful vascular aging and decreasing the risk for cardiovascular disease. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:380 / 401
页数:22
相关论文
共 361 条
[81]   Aging and angiogenesis [J].
Edelberg, JM ;
Reed, MJ .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2003, 8 :S1199-S1209
[82]   Mechanisms involved in the aging-induced vascular dysfunction [J].
El Assar, Mariam ;
Angulo, Javier ;
Vallejo, Susana ;
Peiro, Concepcion ;
Sanchez-Ferrer, Carlos F. ;
Rodriguez-Manas, Leocadio .
FRONTIERS IN PHYSIOLOGY, 2012, 3
[83]   Vascular endothelial senescence: from mechanisms to pathophysiology [J].
Erusalimsky, Jorge D. .
JOURNAL OF APPLIED PHYSIOLOGY, 2009, 106 (01) :326-332
[84]   Xanthine oxidase does not contribute to impaired peripheral conduit artery endothelium-dependent dilatation with ageing [J].
Eskurza, I ;
Kahn, ZD ;
Seals, DR .
JOURNAL OF PHYSIOLOGY-LONDON, 2006, 571 (03) :661-668
[85]   Effect of acute and chronic ascorbic acid on flow-mediated dilatation with sedentary and physically active human ageing [J].
Eskurza, I ;
Monahan, KD ;
Robinson, JA ;
Seals, DR .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 556 (01) :315-324
[86]   RETRACTED: Primary Prevention of Cardiovascular Disease with a Mediterranean Diet (Retracted article. See vol. 378, pg. 2441, 2018) [J].
Estruch, Ramon ;
Ros, Emilio ;
Salas-Salvado, Jordi ;
Covas, Maria-Isabel ;
Corella, Dolores ;
Aros, Fernando ;
Gomez-Gracia, Enrique ;
Ruiz-Gutierrez, Valentina ;
Fiol, Miquel ;
Lapetra, Jose ;
Maria Lamuela-Raventos, Rosa ;
Serra-Majem, Lluis ;
Pinto, Xavier ;
Basora, Josep ;
Angel Munoz, Miguel ;
Sorli, Jose V. ;
Alfredo Martinez, Jose ;
Angel Martinez-Gonzalez, Miguel .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (14) :1279-1290
[87]   Vascular protection - Superoxide dismutase isoforms in the vessel wall [J].
Faraci, FM ;
Didion, SP .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (08) :1367-1373
[88]   Interaction of p53 with Tumor Suppressive and Oncogenic Signaling Pathways to Control Cellular Reactive Oxygen Species Production [J].
Fatima Ladelfa, Maria ;
Fernanda Toledo, Maria ;
Eva Laiseca, Julieta ;
Monte, Martin .
ANTIOXIDANTS & REDOX SIGNALING, 2011, 15 (06) :1749-1761
[89]   The origins of age-related proinflammatory state [J].
Ferrucci, L ;
Corsi, A ;
Lauretani, F ;
Bandinelli, S ;
Bartali, B ;
Taub, DD ;
Guralnik, JM ;
Longo, DL .
BLOOD, 2005, 105 (06) :2294-2299
[90]   SIRT3 Opposes Reprogramming of Cancer Cell Metabolism through HIF1α Destabilization [J].
Finley, Lydia W. S. ;
Carracedo, Arkaitz ;
Lee, Jaewon ;
Souza, Amanda ;
Egia, Ainara ;
Zhang, Jiangwen ;
Teruya-Feldstein, Julie ;
Moreira, Paula I. ;
Cardoso, Sandra M. ;
Clish, Clary B. ;
Pandolfi, Pier Paolo ;
Haigis, Marcia C. .
CANCER CELL, 2011, 19 (03) :416-428