Changes in the blood antioxidant defense of advanced age people

References

• Amalberti, R, Vincent C, Nicklin W,  Braithwaite J. Coping with more people with more illness. Part 1: the nature of the challenge and the implications for safety and quality. Int J Qual Health Care. 2018;31(2):154–158. doi:10.1093/intqhc/mzy235
   Web of Science ®Google Scholar
• Christensen K, Doblhammer G, Rau R, Vaupel JW. Ageing populations: the challenges ahead. Lancet. 2009;374(9696):1196–1208. doi:10.1016/S0140-6736(09)61460-419801098
   PubMed Web of Science ®Google Scholar
• Reeves D, Pye S, Ashcroft DM, et al. The challenge of ageing populations and patient frailty: can primary care adapt? BMJ. 2018;362:k3349. doi:10.1136/bmj.k334930154082
   PubMed Web of Science ®Google Scholar
• Abbing HR. Health, healthcare and ageing populations in Europe, a human rights challenge for European health systems. Eur J Health Law. 2016;23(5):435–452.29210245
   PubMedGoogle Scholar
• Ana Isabel CM, Francisco Ignacio J-R, Margarita R-K, Gill SS, Alicia B-F, Juan Francisco J-B. Down-regulation of arginine decarboxylase gene-expression results in reactive oxygen species accumulation in Arabidopsis. Biochem Biophys Res Commun. 2018;506(4):1071–1077. doi:10.1016/j.bbrc.2018.10.16530409429
   PubMed Web of Science ®Google Scholar
• Jardeleza C, Jones D, Baker L, et al. Gene expression differences in nitric oxide and reactive oxygen species regulation point to an altered innate immune response in chronic rhinosinusitis. Int Forum Allergy Rhinol. 2013;3(3):193–198. doi:10.1002/alr.2111423136082
   PubMed Web of Science ®Google Scholar
• San Martin A, Du P, Dikalova A, et al. Reactive oxygen species-selective regulation of aortic inflammatory gene expression in type 2 diabetes. Am J Physiol Heart Circ Physiol. 2007;292(5):H2073–82. doi:10.1152/ajpheart.00943.200617237245
   PubMed Web of Science ®Google Scholar
• Akram S, Teong HFC, Fliegel L, Pervaiz S, Clément M-V. Reactive oxygen species-mediated regulation of the Na+-H+ exchanger 1 gene expression connects intracellular redox status with cells‘ sensitivity to death triggers. Cell Death Differ. 2006;13(4):628–641. doi:10.1038/sj.cdd.440177516179939
   PubMed Web of Science ®Google Scholar
• Turpaev KT. Reactive oxygen species and regulation of gene expression. Biochemistry (Mosc). 2002;67(3):281–292.11970728
   PubMed Web of Science ®Google Scholar
• Ikeno Y. New insights and current concepts of the oxidative stress theory of aging. Arch Biochem Biophys. 2015;576:1. doi:10.1016/j.abb.2015.03.01925823831
   PubMed Web of Science ®Google Scholar
• Durackova Z. Some current insights into oxidative stress. Physiol Res. 2010;59(4):459–469.19929132
   PubMed Web of Science ®Google Scholar
• Li Y, Nishimura T, Teruya K, et al. Protective mechanism of reduced water against alloxan-induced pancreatic beta-cell damage: scavenging effect against reactive oxygen species. Cytotechnology. 2002;40(1–3):139–149. doi:10.1023/A:102393642144819003114
   PubMed Web of Science ®Google Scholar
• Yu BP. Cellular defenses against damage from reactive oxygen species. Physiol Rev. 1994;74(1):139–162. doi:10.1152/physrev.1994.74.1.1398295932
   PubMed Web of Science ®Google Scholar
• Roy J, Galano J-M, Durand T, Le Guennec J-Y, Lee JC-Y. Physiological role of reactive oxygen species as promoters of natural defenses. FASEB J. 2017;31(9):3729–3745. doi:10.1096/fj.201700170R28592639
   PubMed Web of Science ®Google Scholar
• Barouki R. [Ageing free radicals and cellular stress]. Med Sci (Paris). 2006;22(3):266–272. doi:10.1051/medsci/200622326616527207
   PubMed Web of Science ®Google Scholar
• Poon HF, Calabrese V, Scapagnini G, Butterfield DA. Free radicals: key to brain aging and heme oxygenase as a cellular response to oxidative stress. J Gerontol A Biol Sci Med Sci. 2004;59(5):478–493.15123759
   PubMed Web of Science ®Google Scholar
• Trifunovic A, Wredenberg A, Falkenberg M, et al. Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature. 2004;429(6990):417–423. doi:10.1038/nature0251715164064
   PubMed Web of Science ®Google Scholar
• Kujoth GC, Hiona A, Pugh TD, et al. Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging. Science. 2005;309(5733):481–484. doi:10.1126/science.111212516020738
   PubMed Web of Science ®Google Scholar
• Terzioglu M, Larsson NG. Mitochondrial dysfunction in mammalian ageing. Novartis Found Symp. 2007;287:197–208. discussion 208–13.18074640
   PubMedGoogle Scholar
• Yamasoba T, Lin FR, Someya S, Kashio A, Sakamoto T, Kondo K. Current concepts in age-related hearing loss: epidemiology and mechanistic pathways. Hear Res. 2013;303:30–38. doi:10.1016/j.heares.2013.01.02123422312
   PubMed Web of Science ®Google Scholar
• Bardyn M, Rappaz B, Jaferzadeh K, et al. Red blood cells ageing markers: a multi-parametric analysis. Blood Transfus. 2017;15(3):239–248. doi:10.2450/2017.0318-1628518051
   PubMed Web of Science ®Google Scholar
• Zs-Nagy I. Aging of cell membranes: facts and theories. Interdiscip Top Gerontol. 2014;39:62–85. doi:10.1159/00035890024862015
   PubMedGoogle Scholar
• Valko M, Leibfritz D, Moncol J, Cronin MTD, Mazur M, Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol. 2007;39(1):44–84. doi:10.1016/j.biocel.2006.07.00116978905
   PubMed Web of Science ®Google Scholar
• Reisz JA, Wither MJ, Dzieciatkowska M, et al. Oxidative modifications of glyceraldehyde 3-phosphate dehydrogenase regulate metabolic reprogramming of stored red blood cells. Blood. 2016;128(12):e32–42. doi:10.1182/blood-2016-05-71481627405778
   PubMed Web of Science ®Google Scholar
• Dobi A, Bravo SB, Veeren B, et al. Advanced glycation end-products disrupt human endothelial cells redox homeostasis: new insights into reactive oxygen species production. Free Radic Res. 2019;1–20. doi:10.1080/10715762.2018.1529866
   Web of Science ®Google Scholar
• Vassallo DV, Wiggers GA, Padilha AS, RonacherSimões M. Endothelium:atarget for harmful actions of metals. Curr Hypertens Rev. 2019. doi:10.2174/1573402115666190115153759
   Web of Science ®Google Scholar
• Park SY, Kentish SJ, Wittert GA, Page AJ. Age-related endothelial dysfunction in human skeletal muscle feed arteries: the role of free radicals derived from mitochondria in the vasculature. Acta Physiol (Oxf). 2018;222(1). doi:10.1111/apha.12884
   Web of Science ®Google Scholar
• Harman D. Aging: a theory based on free radical and radiation chemistry. J Gerontol. 1956;11(3):298–300.13332224
   PubMedGoogle Scholar
• Muller FL, Lustgarten MS, Jang Y, Richardson A, Van Remmen H. Trends in oxidative aging theories. Free Radic Biol Med. 2007;43(4):477–503. doi:10.1016/j.freeradbiomed.2007.03.03417640558
   PubMed Web of Science ®Google Scholar
• Perez VI, Bokov A, Van Remmen H, et al. Is the oxidative stress theory of aging dead? Biochim Biophys Acta. 2009;1790(10):1005–1014. doi:10.1016/j.bbagen.2009.06.00319524016
   PubMed Web of Science ®Google Scholar
• Singh S, Singh AK, Garg G, Rizvi SI. Fisetin as a caloric restriction mimetic protects rat brain against aging induced oxidative stress, apoptosis and neurodegeneration. Life Sci. 2018;193:171–179. doi:10.1016/j.lfs.2017.11.00429122553
   PubMed Web of Science ®Google Scholar
• Zanetti M, Gortan Cappellari G, Burekovic I, Barazzoni R, Stebel M, Guarnieri G. Caloric restriction improves endothelial dysfunction during vascular aging: effects on nitric oxide synthase isoforms and oxidative stress in rat aorta. Exp Gerontol. 2010;45(11):848–855. doi:10.1016/j.exger.2010.07.00220637278
   PubMed Web of Science ®Google Scholar
• Sohal RS, Weindruch R. Oxidative stress, caloric restriction, and aging. Science. 1996;273(5271):59–63.8658196
   PubMed Web of Science ®Google Scholar
• Moore A. A new theory of aging based on energy maintenance. Bioessays. 2018;40(8):e1800124. doi:10.1002/bies.v40.830009458
   PubMed Web of Science ®Google Scholar
• Chaudhari SN, Kipreos ET. The energy maintenance theory of aging: maintaining energy metabolism to allow longevity. Bioessays. 2018;40(8):e1800005. doi:10.1002/bies.v40.829901833
   PubMed Web of Science ®Google Scholar
• Cabello-Verrugio C, Vilos C, Rodrigues-Diez R, Estrada L. Oxidative stress in disease and aging: mechanisms and therapies 2018. Oxid Med Cell Longev. 2018;2018:2835189. doi:10.1155/2018/283518930344885
   PubMed Web of Science ®Google Scholar
• Liguori I, Russo G, Curcio F, et al. Oxidative stress, aging, and diseases. Clin Interv Aging. 2018;13:757–772. doi:10.2147/CIA.S15851329731617
   PubMed Web of Science ®Google Scholar
• Simioni C, Zauli G, Martelli AM, et al. Oxidative stress: role of physical exercise and antioxidant nutraceuticals in adulthood and aging. Oncotarget. 2018;9(24):17181–17198. doi:10.18632/oncotarget.2472929682215
   PubMedGoogle Scholar
• Pesce M, Tatangelo R, La Fratta I, et al. Aging-related oxidative stress: positive effect of memory training. Neuroscience. 2018;370:246–255. doi:10.1016/j.neuroscience.2017.09.04628987510
   PubMed Web of Science ®Google Scholar
• Eleutherio E, Brasil ADA, França MB, de Almeida DSG, Rona GB, Magalhães RSS. Oxidative stress and aging: learning from yeast lessons. Fungal Biol. 2018;122(6):514–525. doi:10.1016/j.funbio.2017.12.00329801796
   PubMed Web of Science ®Google Scholar
• Lee JY, Paik IY, Kim JY. Voluntary exercise reverses immune aging induced by oxidative stress in aging mice. Exp Gerontol. 2019;115:148–154. doi:10.1016/j.exger.2018.08.009
   Web of Science ®Google Scholar
• Zhou HJ, Zeng C-Y, Yang -T-T, Long F-Y, Kuang X, Du J-R. Lentivirus-mediated klotho up-regulation improves aging-related memory deficits and oxidative stress in senescence-accelerated mouse prone-8 mice. Life Sci. 2018;200:56–62. doi:10.1016/j.lfs.2018.03.02729544758
   PubMed Web of Science ®Google Scholar
• Kirkwood TB, Kowald A. The free-radical theory of ageing–older, wiser and still alive: modelling positional effects of the primary targets of ROS reveals new support. Bioessays. 2012;34(8):692–700. doi:10.1002/bies.20120001422641614
   PubMed Web of Science ®Google Scholar
• Pomatto LCD, Davies KJA. Adaptive homeostasis and the free radical theory of ageing. Free Radic Biol Med. 2018;124:420–430. doi:10.1016/j.freeradbiomed.2018.06.01629960100
   PubMed Web of Science ®Google Scholar
• Placer ZA, Cushman LL, Johnson BC. Estimation of product of lipid peroxidation (malonyl dialdehyde) in biochemical systems. Anal Biochem. 1966;16(2):359–364.6007581
   PubMed Web of Science ®Google Scholar
• Misra HP, Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem. 1972;247(10):3170–3175.4623845
   PubMed Web of Science ®Google Scholar
• Beers RF Jr., Sizer IW. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem. 1952;195(1):133–140.14938361
   PubMed Web of Science ®Google Scholar
• Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967;70(1):158–169.6066618
   PubMed Web of Science ®Google Scholar
• Flohe L, Gunzler WA. Assays of glutathione peroxidase. Methods Enzymol. 1984;105:114–121.6727659
   PubMed Web of Science ®Google Scholar
• Roth E, Hejjel L, Jaberansari M, Jancso G. The role of free radicals in endogenous adaptation and intracellular signals. Exp Clin Cardiol. 2004;9(1):13–16.19641690
   PubMedGoogle Scholar
• Terashvili M, Pratt PF, Gebremedhin D, Narayanan J, Harder DR. Reactive oxygen species cerebral autoregulation in health and disease. Pediatr Clin North Am. 2006;53(5):1029–37.xi. doi:10.1016/j.pcl.2006.08.00317027622
   PubMed Web of Science ®Google Scholar
• Afanas‘Ev IB. On mechanism of superoxide signaling under physiological and pathophysiological conditions. Med Hypotheses. 2005;64(1):127–129. doi:10.1016/j.mehy.2004.05.00915533629
   PubMed Web of Science ®Google Scholar
• Forman HJ. Redox signaling: an evolution from free radicals to aging. Free Radic Biol Med. 2016;97:398–407. doi:10.1016/j.freeradbiomed.2016.07.00327393004
   PubMed Web of Science ®Google Scholar
• Kasapoglu M, Ozben T. Alterations of antioxidant enzymes and oxidative stress markers in aging. Exp Gerontol. 2001;36(2):209–220.11226737
   PubMed Web of Science ®Google Scholar
• Inal ME, Kanbak G, Sunal E. Antioxidant enzyme activities and malondialdehyde levels related to aging. Clin Chim Acta. 2001;305(1–2):75–80.11249925
   PubMed Web of Science ®Google Scholar
• Sohal RS. Role of oxidative stress and protein oxidation in the aging process. Free Radic Biol Med. 2002;33(1):37–44.12086680
   PubMed Web of Science ®Google Scholar
• Sato M, Yanagisawa H, Nojima Y, Tamura J, Wada O. Zn deficiency aggravates hypertension in spontaneously hypertensive rats: possible role of Cu/Zn-superoxide dismutase. Clin Exp Hypertens. 2002;24(5):355–370.12109776
   PubMed Web of Science ®Google Scholar
• Holben DH, Smith AM. The diverse role of selenium within selenoproteins: a review. J Am Diet Assoc. 1999;99(7):836–843. doi:10.1016/S0002-8223(99)00198-410405682
   PubMedGoogle Scholar
• Maharaj DS, Glass BD, Daya S. Melatonin: new places in therapy. Biosci Rep. 2007;27(6):299–320. doi:10.1007/s10540-007-9052-117828452
   PubMed Web of Science ®Google Scholar
• Yanar K, Simsek B, Cakatay U. Integration of melatonin related redox homeostasis, aging and circadian rhythm. Rejuvenation Res. 2018. doi:10.1089/rej.2018.2159
   Web of Science ®Google Scholar
• Yang Y, Cheung -H-H, Zhang C, Wu J, Chan W-Y. Melatonin as potential targets for delaying ovarian aging. Curr Drug Targets. 2019;20(1):16–28. doi:10.2174/138945011966618082814484330156157
   PubMed Web of Science ®Google Scholar
• Marzani B, Felzani G, Bellomo RG, Vecchiet J, Marzatico F. Human muscle aging: ROS-mediated alterations in rectus abdominis and vastus lateralis muscles. Exp Gerontol. 2005;40(12):959–965. doi:10.1016/j.exger.2005.08.01016213688
   PubMed Web of Science ®Google Scholar
• Al-Abrash AS, Al-Quobaili FA, Al-Akhras GN. Catalase evaluation in different human diseases associated with oxidative stress. Saudi Med J. 2000;21(9):826–830.11376358
   PubMed Web of Science ®Google Scholar
• Flores-Mateo G, Elosua R, Rodriguez-Blanco T, et al. Oxidative stress is associated with an increased antioxidant defense in elderly subjects: a multilevel approach. PLoS One. 2014;9(9):e105881. doi:10.1371/journal.pone.010588125269026
   PubMed Web of Science ®Google Scholar
• Klapcinska B, Derejczyk J, Wieczorowska-Tobis K, Sobczak A, Sadowska-Krepa E, Danch A. Antioxidant defense in centenarians (a preliminary study). Acta Biochim Pol. 2000;47(2):281–292.11051193
   PubMed Web of Science ®Google Scholar
• Spiteller G. The important role of lipid peroxidation processes in aging and age dependent diseases. Mol Biotechnol. 2007;37(1):5–12.17914157
   PubMed Web of Science ®Google Scholar
• Spiteller G. Lipid peroxidation in aging and age-dependent diseases. Exp Gerontol. 2001;36(9):1425–1457.11525868
   PubMed Web of Science ®Google Scholar
• Girotti AW. Lipid hydroperoxide generation, turnover, and effector action in biological systems. J Lipid Res. 1998;39(8):1529–1542.9717713
   PubMed Web of Science ®Google Scholar
• Yavuzer H, Yavuzer S, Cengiz M, et al. Biomarkers of lipid peroxidation related to hypertension in aging. Hypertens Res. 2016;39(5):342–348. doi:10.1038/hr.2015.15626763852
   PubMed Web of Science ®Google Scholar
• Pratico D. Lipid peroxidation and the aging process. Sci Aging Knowledge Environ. 2002;2002(50):re5.14603026
   PubMedGoogle Scholar
• Salminen LE, Paul RH. Oxidative stress and genetic markers of suboptimal antioxidant defense in the aging brain: a theoretical review. Rev Neurosci. 2014;25(6):805–819. doi:10.1515/revneuro-2014-004625153586
   PubMed Web of Science ®Google Scholar