Longevity is associated with increased vascular resistance to high glucose-induced oxidative stress and inflammatory gene expression in Peromyscus leucopus

被引:46
作者
Labinskyy, Nazar [1 ]
Mukhopadhyay, Partha [2 ]
Toth, Janos [1 ]
Szalai, Gabor [3 ,4 ]
Veres, Monika [3 ,4 ]
Losonczy, Gyorgy [5 ]
Pinto, John T. [6 ]
Pacher, Pal [2 ]
Ballabh, Praveen [7 ,8 ]
Podlutsky, Andrej [9 ]
Austad, Steven N. [9 ]
Csiszar, Anna [1 ]
Ungvari, Zoltan [1 ,5 ]
机构
[1] New York Med Coll, Dept Physiol, Valhalla, NY 10595 USA
[2] NIAAA, Lab Physiol Studies, Sect Oxidat Stress Tissue Injury, Bethesda, MD USA
[3] Univ S Carolina, Dept Biol Sci, Columbia, SC 29208 USA
[4] Univ S Carolina, Peromyscus Stock Ctr, Columbia, SC 29208 USA
[5] Semmelweis Univ, Dept Pulm, H-1085 Budapest, Hungary
[6] New York Med Coll, Dept Biochem, Valhalla, NY 10595 USA
[7] New York Med Coll, Dept Cell Biol & Anat, Valhalla, NY 10595 USA
[8] New York Med Coll, Dept Pediat, Valhalla, NY 10595 USA
[9] Univ Texas Hlth Sci Ctr San Antonio, Sam & Ann Barshop Inst Longev & Aging Studies, San Antonio, TX 78229 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2009年 / 296卷 / 04期
基金
匈牙利科学研究基金会; 美国国家卫生研究院;
关键词
senescence; comparative biology; vascular disease; atherosclerosis; HYDROGEN-PEROXIDE PRODUCTION; MITOCHONDRIAL SUPEROXIDE-PRODUCTION; FREE-RADICAL PRODUCTION; LONGEST-LIVING RODENT; NAKED MOLE-RAT; H2O2; PRODUCTION; LIFE-SPAN; ENDOTHELIAL DYSFUNCTION; HEART-MITOCHONDRIA; CORONARY-ARTERIES;
D O I
10.1152/ajpheart.00693.2008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Labinskyy N, Mukhopadhyay P, Toth J, Szalai G, Veres M, Losonczy G, Pinto JT, Pacher P, Ballabh P, Podlutsky A, Austad SN, Csiszar A, Ungvari Z. Longevity is associated with increased vascular resistance to high glucose-induced oxidative stress and inflammatory gene expression in Peromyscus leucopus. Am J Physiol Heart Circ Physiol 296: H946-H956, 2009. First published January 30, 2009; doi:10.1152/ajpheart.00693.2008.-Vascular aging is characterized by increased oxidative stress and proinflammatory phenotypic alterations. Metabolic stress, such as hyperglycemia in diabetes, is known to increase the production of ROS and promote inflammatory gene expression, accelerating vascular aging. The oxidative stress hypothesis of aging predicts that vascular cells of long-lived species exhibit lower steady-state production of ROS and/or superior resistance to the prooxidant effects of metabolic stress. We tested this hypothesis using two taxonomically related rodents, the white-footed mouse (Peromyscus leucopus) and the house mouse (Mus musculus), which show a more than twofold difference in maximum lifespan potential (8.2 and 3.5 yr, respectively). We compared interspecies differences in steady-state and high glucose (HG; 30 mmol/l)-induced production of O-2(center dot-) and H2O2, endothelial function, mitochondrial ROS generation, and inflammatory gene expression in cultured aortic segments. In P. leucopus aortas, steady- state endothelial O-2(center dot-) and H2O2 production and ROS generation by mitochondria were less than in M. musculus vessels. Furthermore, vessels of P. leucopus were more resistant to the prooxidant effects of HG. Primary fibroblasts from P. leucopus also exhibited less steady- state and HG-induced ROS production than M. musculus cells. In M. musculus arteries, HG elicited significant up-regulation of inflammatory markers (TNF-alpha, IL-6, ICAM-1, VCAM, and monocyte chemoattractant protein-1). In contrast, the proinflammatory effects of HG were blunted in P. leucopus vessels. Thus, increased life span potential in P. leucopus is associated with decreased cellular ROS generation and increased resistance to prooxidant and proinflammatory effects of metabolic stress, which accord with predictions of the oxidative stress hypothesis of aging.
引用
收藏
页码:H946 / H956
页数:11
相关论文
共 63 条
[1]   NAD(P)H oxidase-generated superoxide anion accounts for reduced control of myocardial O2 consumption by NO in old Fischer 344 rats [J].
Adler, A ;
Messina, E ;
Sherman, B ;
Wang, ZP ;
Huang, H ;
Linke, A ;
Hintze, TH .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (03) :H1015-H1022
[2]   Association between a functional variant of the KLOTHO gene and high-density lipoprotein cholesterol, blood pressure, stroke, and longevity [J].
Arking, DE ;
Atzmon, G ;
Arking, A ;
Barzilai, N ;
Dietz, HC .
CIRCULATION RESEARCH, 2005, 96 (04) :412-418
[3]   Lipoprotein genotype and conserved pathway for exceptional longevity in humans [J].
Atzmon, G ;
Rincon, M ;
Schechter, CB ;
Shuldiner, AR ;
Lipton, RB ;
Bergman, A ;
Barzilai, N .
PLOS BIOLOGY, 2006, 4 (04) :562-569
[4]   MAMMALIAN AGING, METABOLISM, AND ECOLOGY - EVIDENCE FROM THE BATS AND MARSUPIALS [J].
AUSTAD, SN ;
FISCHER, KE .
JOURNALS OF GERONTOLOGY, 1991, 46 (02) :B47-B53
[5]   An experimental paradigm for the study of slowly aging organisms [J].
Austad, SN .
EXPERIMENTAL GERONTOLOGY, 2001, 36 (4-6) :599-605
[6]   Mitochondria, oxidants, and aging [J].
Balaban, RS ;
Nemoto, S ;
Finkel, T .
CELL, 2005, 120 (04) :483-495
[7]   Localization at complex I and mechanism of the higher free radical production of brain nonsynaptic mitochondria in the short-lived rat than in the longevous pigeon [J].
Barja, G ;
Herrero, A .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1998, 30 (03) :235-243
[8]   The free radical theory of aging matures [J].
Beckman, KB ;
Ames, BN .
PHYSIOLOGICAL REVIEWS, 1998, 78 (02) :547-581
[9]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[10]   Reduced free-radical production and extreme longevity in the little brown bat (Myotis lucifugus) versus two non-flying mammals [J].
Brunet-Rossinni, AK .
MECHANISMS OF AGEING AND DEVELOPMENT, 2004, 125 (01) :11-20