The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: current state
Open accessAbstract
Remarkable interest has risen in the idea that oxidative/nitrosative stress is mediated in the etiology of numerous human diseases. Oxidative/Nitrosative stress is the result of an disequilibrium in oxidant/antioxidant which reveals from continuous increase of Reactive Oxygen and Reactive Nitrogen Species production. The aim of this review is to emphasize with current information the importance of antioxidants which play the role in cellular responce against oxidative/nitrosative stress, which would be helpful in enhancing the knowledge of any biochemist, pathophysiologist, or medical personnel regarding this important issue. Products of lipid peroxidation have commonly been used as biomarkers of oxidative/nitrosative stress damage. Lipid peroxidation generates a variety of relatively stable decomposition end products, mainly α, β-unsaturated reactive aldehydes, such as malondialdehyde, 4-hydroxy-2-nonenal, 2-propenal (acrolein) and isoprostanes, which can be measured in plasma and urine as an indirect index of oxidative/nitrosative stress. Antioxidants are exogenous or endogenous molecules that mitigate any form of oxidative/nitrosative stress or its consequences. They may act from directly scavenging free radicals to increasing antioxidative defences. Antioxidant deficiencies can develop as a result of decreased antioxidant intake, synthesis of endogenous enzymes or increased antioxidant utilization. Antioxidant supplementation has become an increasingly popular practice to maintain optimal body function. However, antoxidants exhibit pro-oxidant activity depending on the specific set of conditions. Of particular importance are their dosage and redox conditions in the cell.
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Vitamin E protects against lipid peroxidation, which produces metabolites associated with oxidative stress.
“Vitamin E works as an antioxidant by conferring protection against lipid peroxidation, which produces metabolites associated with oxidative stress143.”
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- [1]Kurutas EB Ciragil P Gul M Kilinc M The effects of oxidative stress in urinary tract infection Mediators Inflamm 2005 2005 242 244 10.1155/MI.2005.242 16192676 PMC1526480 · DOI
- [2]Valko M Leibfritz D Moncol J Cronin MT Mazur M Telser J Free radicals and antioxidants in normal physiological functions and human disease Int J Biochem Cell Biol 2007 39 44 84 10.1016/j.biocel.2006.07.001 16978905 · DOI · Paper page
- [3]Barbacanne MA Souchard JP Darblade B Iliou JP Nepveu F Pipy B Bayard F Arnal JF Detection of superoxide anion released extracellularly by endothelial cells using cytochrome c reduction, ESR, fluorescence and lucigenin-enhanced chemiluminescence techniques Free Radic Biol Med 2000 29 388 96 10.1016/S0891-5849(00)00336-1 11020659 · DOI
- [4]Vidrio E Jung H Anastasio C Generation of Hydroxyl Radicals from Dissolved Transition Metals in Surrogate Lung Fluid Solutions Atmos Environ 2008 42 4369 4379 10.1016/j.atmosenv.2008.01.004 PMC2626252 19148304 · DOI
- [5]Murphy E Steenbergen C Mechanisms underlying acute protection from cardiac ischemia-reperfusion injury Physiol Rev 2008 88 581 609 10.1152/physrev.00024.2007 18391174 PMC3199571 · DOI
- [6]Bortoletto P Lyman K Camacho A Fricchione M Khanolkar A Katz BZ Chronic granulomatous disease Pediatr Infect Dis J 2015 34 1110 1114 10.1097/INF.0000000000000840 26181896 PMC4568897 · DOI
- [8]Masters CJ Cellular signalling: the role of the peroxisome Cell Signal 1996 8 197 208 10.1016/0898-6568(95)02055-1 8736704 · DOI
- [9]Cederbaum AI Molecular mechanisms of the microsomal mixed function oxidases and biological and pathological implications Redox Biol 2015 4 60 73 10.1016/j.redox.2014.11.008 25498968 PMC4309856 · DOI
- [10]Dröge W Free radicals in the physiological control of cell function Physiol Rev 2002 82 47 95 10.1152/physrev.00018.2001 11773609 · DOI · Paper page
- [12]Tatsuzawa H Maruyama T Hori K Sano Y Nakano M Singlet oxygen ((1)Delta(g)O(2)) as the principal oxidant in myeloperoxidase-mediated bacterial killing in neutrophil phagosomes Biochim Biophys Res Commun 1999 262 647 650 10.1006/bbrc.1999.1265 10471379 · DOI
- [13]Lloyd RV Hanna PM Mason RP The origin of the hydroxyl radical oxygen in the Fenton reaction Free Radic Biol Med 1997 22 885 888 10.1016/S0891-5849(96)00432-7 9119257 · DOI
- [15]Pepper JR Mumby S Gutteridge JC Sequential oxidative damage, and changes in iron binding and iron oxidizing plasma antioxidants during cardiopulmonary bypass surgery Free Radic Res 1994 21 377 85 10.3109/10715769409056590 7834052 · DOI
- [16]Jomova K Valko M Importance of iron chelation in free radical-induced oxidative stress and human disease Curr Pharm Des 2011 17 3460 73 10.2174/138161211798072463 21902663 · DOI
- [17]Saito H Hayashi H Transformation rate between ferritin and hemosiderin assayed by serum ferritin kinetics in patients with normal iron stores and iron overload Nagoya J Med Sci 2015 77 571 83 26663936 PMC4664589
- [18]Ghafourifar P Cadenas E Mitochondrial nitric oxide synthase Trends Pharmacol Sci 2005 26 190 195 10.1016/j.tips.2005.02.005 15808343 · DOI
- [19]Bergendi L Benes L Durackova Z Ferencik M Chemistry, physiology and pathology of free radicals Life Sci 1999 65 1865 1874 10.1016/S0024-3205(99)00439-7 10576429 · DOI
- [20]Chiueh CC Neuroprotective properties of nitric oxide Ann NY Acad Sci 1999 890 301 311 10.1111/j.1749-6632.1999.tb08007.x 10668435 · DOI
- [21]Beckman JS Koppenol WH Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly Am J Physiol 1996 271 C1424 37 8944624
- [22]Pacher P Beckman JS Liaudet L Nitric oxide and peroxynitrite in health and disease Physiol Rev 2007 87 315 424 10.1152/physrev.00029.2006 17237348 PMC2248324 · DOI · Paper page
- [23]Young IS Woodside JV Antioxidants in health and disease J Clin Pathol 2001 54 176 186 10.1136/jcp.54.3.176 11253127 PMC1731363 · DOI · Paper page
- [24]Flora SJ Structural, chemical and biological aspects of antioxidants for strategies against metal and metalloid exposure Oxid Med Cell Longev 2009 2 191 206 10.4161/oxim.2.4.9112 20716905 PMC2763257 · DOI
- [25]Finkel T Holbrook NJ Oxidants, oxidative stress and the biology of ageing Nature 2000 408 239 247 10.1038/35041687 11089981 · DOI · Paper page
- [26]Uchida K 4-Hydroxy-2-nonenal: a product and mediator of oxidative stress Prog Lipid Res 2003 42 318 343 10.1016/S0163-7827(03)00014-6 12689622 · DOI · Paper page
- [27]Carini M Aldini G Facino RM Mass spectrometry for detection of 4-hydroxy-trans-2- onenal (HNE) adducts with peptides and proteins Mass Spectrom Rev 2004 23 281 305 10.1002/mas.10076 15133838 · DOI
- [28]Cracowski JL Durand T Bessard G Isoprostanes as a biomarker of lipid peroxidation in humans: physiology, pharmacology and clinical implications Trends Pharmacol Sci 2002 23 360 366 10.1016/S0165-6147(02)02053-9 12377577 · DOI
- [29]Montuschi P Barnes PJ Roberts LJ Isoprostanes: markers and mediators of oxidative stress FASEB J 2004 18 1791 1800 10.1096/fj.04-2330rev 15576482 · DOI
- [30]Uchida K Histidine and lysine as targets of oxidative modification Amino Acids 2003 25 249 257 10.1007/s00726-003-0015-y 14661088 · DOI
- [31]Draper HH Csallany AS Hadley M Urinary aldehydes as indicators of lipid peroxidation in vivo Free Radic Biol Med 2000 29 1071 1077 10.1016/S0891-5849(00)00367-1 11121713 · DOI
- [32]Wilson R Lyall K Smyth L Fernie CE Riemersma RA Dietary hydroxy fatty acids are absorbed in humans: implications for the measurement of ‘oxidative stress’ in vivo Free Radic Biol Med 2002 32 162 168 10.1016/S0891-5849(01)00780-8 11796205 · DOI
- [33]Basu S Isoprostanes: novel bioactive products of lipid peroxidation Free Radic Res 2004 38 105 122 10.1080/10715760310001646895 15104204 · DOI
- [34]Miraloglu M Kurutas EB Ozturk P Arican O Evaluation of local trace element status and 8-Iso-prostaglandin F2α concentrations in patients with Tinea pedis Biol Proced Online 2016 18 1 10.1186/s12575-015-0030-x 26740800 PMC4702401 · DOI
- [35]Morrow JD Quantification of isoprostanes as indices of oxidant stress and the risk of atherosclerosis in humans Arterioscler Thromb Vasc Biol 2005 25 279 286 10.1161/01.ATV.0000152605.64964.c0 15591226 · DOI
- [36]Moret-Tatay I Iborra M Cerrillo E Tortosa L Nos P Beltrán B Possible Biomarkers in Blood for Crohn’s Disease: Oxidative Stress and MicroRNAs-Current Evidences and Further Aspects to Unravel Oxid Med Cell Longev 2016 2016 2325162 10.1155/2016/2325162 26823944 PMC4707323 · DOI
- [37]Poli G Leonarduzzi G Biasi F Chiarpotto E Oxidative stress and cell signalling Curr Med Chem 2004 11 1163 1182 10.2174/0929867043365323 15134513 · DOI
- [38]Eizirik DL Manndrup-Poulsen T A chice of death - the signaltransduction of immuneimediated beta-cell apoptosis Diabetologia 2001 44 2115 2133 10.1007/s001250100021 11793013 · DOI
- [39]Buttke TM Sandstrom PA Oxidative stress as mediator of apoptosis Immunol Today 1994 15 1 4 10.1016/0167-5699(94)90018-3 8136014 · DOI
- [40]Niki E Free Radicals in the 1900’s: from in vitro to in vivo Free Radic Res 2001 33 693 704 10.1080/10715760000301221 11237092 · DOI
- [41]Klaunig JE Kamendulis LM Hocevar BA Oxidative stress and oxidative damage in carcinogenesis Toxicol Pathol 2010 38 96 109 10.1177/0192623309356453 20019356 · DOI
- [42]Pavlovic D Kocic R Kocic G Jevtovic T Radenkovic S Mikic D Stojanovic M Djordjevic PB Effect of a four week metformin treatment on plasma and erythrocyte antioxidative defense enzymes in newly diagnosed obese NIDDM patientes Diabetes Obes Metab 2000 2 251 6 10.1046/j.1463-1326.2000.00089.x 11225659 · DOI
- [43]Diaz MN Frei B Vita JA Keaney JF Antioxidants and atherosclerotic heart disease N Engl J Med 1997 337 408 416 10.1056/NEJM199708073370607 9241131 · DOI
- [44]Marinho HS Real C Cyrne L Soares H Antunes F Hydrogen peroxide sensing, signaling and transcription factors regulation Redox Biol 2014 2 535 562 10.1016/j.redox.2014.02.006 24634836 PMC3953959 · DOI
- [45]Nabavi SF Barber AJ Spagnuolo C Russo GL Daglia M Nabavi SM Sobarzo-Sánchez E Nrf2 as molecular target for polyphenols: A novel therapeutic strategy in diabetic retinopathy Crit Rev Clin Lab Sci 2016 29 1 20 26926494
- [46]Pang C Sheng Y Jiang P Wei H Ji L Chlorogenic acid prevents acetaminophen-induced liver injury: the involvement of CYP450 metabolic enzymes and some antioxidant signals J Zhejiang Univ Sci B 2015 16 602 610 10.1631/jzus.B1400346 26160718 PMC4506951 · DOI
- [47]Prasad KN Simultaneous Activation of Nrf2 and Elevation of Dietary and Endogenous Antioxidant Chemicals for Cancer Prevention in Humans J Am Coll Nutr 2016 35 175 84 10.1080/07315724.2014.1003419 26151600 · DOI
- [48]Chan K Han XD Kan YW An important function of Nrf2 in combating oxidative stress: detoxification of acetaminophen Proc Natl Acad Sci U S A 2001 98 4611 6 10.1073/pnas.081082098 11287661 PMC31882 · DOI
- [49]Enomoto A Itoh K Nagayoshi E Haruta J Kimura T O’Connor T Harada T Yamamoto M High sensitivity of Nrf2 knockout mice to acetaminophen hepatotoxicity associated with decreased expression of ARE-regulated drug metabolizing enzymes and antioxidant genes Toxicol Sci 2001 59 169 77 10.1093/toxsci/59.1.169 11134556 · DOI · Paper page
- [50]Chan K Kan YW Nrf2 is essential for protection against acute pulmonary injury in mice Proc Natl Acad Sci U S A 1999 96 12731 6 10.1073/pnas.96.22.12731 10535991 PMC23072 · DOI · Paper page
- [51]Fahey JW Haristoy X Dolan PM Kensler TW Scholtus I Stephenson KK Talalay P Lozniewski A Sulforaphane inhibits extracellular, intracellular, and antibiotic-resistant strains of Helicobacter pylori and prevents benzo[a]pyrene-induced stomach tumors Proc Natl Acad Sci U S A 2002 99 7610 5 10.1073/pnas.112203099 12032331 PMC124299 · DOI
- [52]Ramos-Gomez M Kwak MK Dolan PM Itoh K Yamamoto M Talalay P Kensler TW Sensitivity to carcinogenesis is increased and chemoprotective efficacy of enzyme inducers is lost in nrf2 transcription factor-deficient mice Proc Natl Acad Sci U S A 2001 98 3410 5 10.1073/pnas.051618798 11248092 PMC30667 · DOI · Paper page
- [54]Dhakshinamoorthy S Long DJ Jaiswal AK Antioxidant regulation of genes encoding enzymes that detoxify xenobiotics and carcinogens Curr Top Cell Regul 2000 36 201 16 10.1016/S0070-2137(01)80009-1 10842753 · DOI
- [55]Lee JM Moehlenkamp JD Hanson JM Johnson JA Nrf2-dependent activation of the antioxidant responsive element by tert-butylhydroquinone is independent of oxidative stress in IMR-32 human neuroblastoma cells Biochem Biophys Res Commun 2001 280 286 92 10.1006/bbrc.2000.4106 11162512 · DOI
- [56]Lee JM Hanson JM Chu WA Johnson JA Phosphatidylinositol 3-kinase, not extracellular signal-regulated kinase, regulates activation of the antioxidant-responsive element in IMR-32 human neuroblastoma cells J Biol Chem 2001 276 20011 6 10.1074/jbc.M100734200 11274155 · DOI
- [57]Alam J Wicks C Stewart D Gong P Touchard C Otterbein S Choi AM Burow ME Tou J Mechanism of heme oxygenase-1 gene activation by cadmium in MCF-7 mammary epithelial cells. Role of p38 kinase and Nrf2 transcription factor J Biol Chem 2000 275 27694 702 10874044
- [58]Kim YC Masutani H Yamaguchi Y Itoh K Yamamoto M Yodoi J Hemin-induced activation of the thioredoxin gene by Nrf2. A differential regulation of the antioxidant responsive element by a switch of its binding factors J Biol Chem 2001 276 18399 406 10.1074/jbc.M100103200 11279008 · DOI
- [60]Motohashi H O’Connor T Katsuoka F Engel JD Yamamoto M Integration and diversity of the regulatory network composed of Maf and CNC families of transcription factors Gene 2002 294 1 12 10.1016/S0378-1119(02)00788-6 12234662 · DOI
- [61]Chanas SA Jiang Q McMahon M McWalter GK McLellan LI Elcombe CR Henderson CJ Wolf CR Moffat GJ Itoh K Yamamoto M Hayes JD Loss of the Nrf2 transcription factor causes a marked reduction in constitutive and inducible expression of the glutathione S-transferase Gsta1, Gsta2, Gstm1, Gstm2, Gstm3 and Gstm4 genes in the livers of male and female mice Biochem J 2002 365 405 16 10.1042/bj20020320 11991805 PMC1222698 · DOI · Paper page
- [62]Hayes JD Chanas SA Henderson CJ McMahon M Sun C Moffat GJ Wolf CR Yamamoto M The Nrf2 transcription factor contributes both to the basal expression of glutathione S-transferases in mouse liver and to their induction by the chemopreventive synthetic antioxidants, butylated hydroxyanisole and ethoxyquin Biochem Soc Trans 2000 28 33 41 10.1042/bst0280033 10816095 · DOI
- [63]Ishii T Itoh K Takahashi S Sato H Yanagawa T Katoh Y Bannai S Yamamoto M Transcription factor Nrf2 coordinately regulates a group of oxidative stress-inducible genes in macrophages J Biol Chem 2000 275 16023 9 10.1074/jbc.275.21.16023 10821856 · DOI
- [64]Nguyen T Huang HC Pickett CB Transcriptional regulation of the antioxidant response element. Activation by Nrf2 and repression by MafK J Biol Chem 2000 275 15466 73 10.1074/jbc.M000361200 10747902 · DOI
- [65]Wild AC Moinova HR Mulcahy RT Regulation of gamma-glutamylcysteine synthetase subunit gene expression by the transcription factor Nrf2 J Biol Chem 1999 274 33627 36 10.1074/jbc.274.47.33627 10559251 · DOI
- [66]Alam J Stewart D Touchard C Boinapally S Choi AM Cook JL Nrf2, a Cap’n’Collar transcription factor, regulates induction of the heme oxygenase-1 gene J Biol Chem 1999 274 26071 8 10.1074/jbc.274.37.26071 10473555 · DOI
- [67]Yu R Lei W Mandlekar S Weber MJ Der CJ Wu J Kong AN Role of a mitogen-activated protein kinase pathway in the induction of phase II detoxifying enzymes by chemicals J Biol Chem 1999 274 27545 52 10.1074/jbc.274.39.27545 10488090 · DOI
- [68]Huang HC Nguyen T Pickett CB Regulation of the antioxidant response element by protein kinase C-mediated phosphorylation of NF-E2-related factor 2 Proc Natl Acad Sci U S A 2000 97 12475 8031 10.1073/pnas.220418997 11035812 PMC18788 · DOI
- [69]Li J Lee JM Johnson JA Microarray analysis reveals an antioxidant responsive element-driven gene set involved in conferring protection from an oxidative stress-induced apoptosis in IMR-32 cells J Biol Chem 2002 277 388 94 10.1074/jbc.M109380200 11687587 · DOI
- [70]Li J Johnson JA Time-dependent changes in ARE-driven gene expression by use of a noise-filtering process for microarray data Physiol Genomics 2002 9 137 44 10.1152/physiolgenomics.00003.2002 12045294 · DOI
- [71]Johnson DA Andrews GK Xu W Johnson JA Activation of the antioxidant response element in primary cortical neuronal cultures derived from transgenic reporter mice J Neurochem 2002 81 1233 41 10.1046/j.1471-4159.2002.00913.x 12068071 · DOI
- [72]Kang KW Cho MK Lee CH Kim SG Activation of phosphatidylinositol 3-kinase and Akt by tert-butylhydroquinone is responsible for antioxidant response element-mediated rGSTA2 induction in H4IIE cells Mol Pharmacol 2001 59 1147 56 11306698
- [73]Lee JM Johnson JA An important role of Nrf2-ARE pathway in the cellular defense mechanism J Biochem Mol Biol 2004 37 139 43 10.5483/BMBRep.2004.37.2.139 15469687 · DOI
- [75]Niture SK Khatri R Jaiswal AK Regulation of Nrf2 – an update Free Radic Biol Med 2014 66 34 36 10.1016/j.freeradbiomed.2013.02.008 PMC3773280 23434765 · DOI
- [76]Forman HJ Davies KJA Ursini F How do nutritional antioxidants really work: nucleophilic tone and para-hormesis free radical scavenging in vivo Free Radic Biol Med 2014 66 24 35 10.1016/j.freeradbiomed.2013.05.045 23747930 PMC3852196 · DOI
- [77]Vnukov VV Gutsenko OI Milutina NP Ananyan AA Danilenko AO Panina SB Kornienko IV Influence of SkQ1 on expression of Nrf2 transcription factor gene, ARE-controlled genes of antioxidant enzymes, and their activity in rat blood leukocytes Biochemistry (Mosc) 2015 80 586 591 10.1134/S0006297915050107 26071777 · DOI
- [78]Itoh K Mimura J Yamamoto M Discovery of the negative regulator of Nrf2, Keap1: a historical overview Antioxid Redox Signal 2010 13 1665 78 10.1089/ars.2010.3222 20446768 · DOI
- [79]Kensler TW Wakabayashi N Nrf2: friend or foe for chemoprevention? Carcinogenesis 2010 31 90 9 10.1093/carcin/bgp231 19793802 PMC2802668 · DOI
- [80]Solis LM Behrens C Dong W Suraokar M Ozburn NC Moran CA Corvalan AH Biswal S Swisher SG Bekele BN Minna JD Stewart DJ Wistuba II Nrf2 and Keap1 abnormalities in non-small cell lung carcinoma and association with clinicopathologic features Clin Cancer Res 2010 16 3743 53 10.1158/1078-0432.CCR-09-3352 20534738 PMC2920733 · DOI
- [81]Singh A Misra V Thimmulappa RK Lee H Ames S Hoque MO Herman JG Baylin SB Sidransky D Gabrielson E Brock MV Biswal S Dysfunctional KEAP1-NRF2 interaction in non-small-cell lung cancer PLoS Med 2006 3 e420 10.1371/journal.pmed.0030420 17020408 PMC1584412 · DOI · Paper page
- [82]Shibata T Kokubu A Gotoh M Ojima H Ohta T Yamamoto M Hirohashi S Genetic alteration of Keap1 confers constitutive Nrf2 activation and resistance to chemotherapy in gallbladder cancer Gastroenterol 2008 135 1358 68 10.1053/j.gastro.2008.06.082 18692501 · DOI
- [83]Li K Zhong C Wang B He J Bi J Nrf2 expression participates in growth and differentiation of endometrial carcinoma cells in vitro and in vivo J Mol Histol 2014 45 161 7 10.1007/s10735-013-9538-z 24048968 · DOI
- [84]Zhang P Singh A Yegnasubramanian S Esopi D Kombairaju P Bodas M Wu H Bova SG Biswal S Loss of Kelch-like ECH-associated protein 1 function in prostate cancer cells causes chemoresistance and radioresistance and promotes tumor growth Mol Cancer Ther 2010 9 336 46 10.1158/1535-7163.MCT-09-0589 20124447 PMC2821808 · DOI
- [85]Ji XJ Chen SH Zhu L Pan H Zhou Y Li W You WC Gao CC Zhu JH Jiang K Wang HD Knockdown of NF-E2-related factor 2 inhibits the proliferation and growth of U251MG human glioma cells in a mouse xenograft model Oncol Rep 2013 30 157 64 23673813
- [86]Soini Y Eskelinen M Juvonen P Kärjä V Haapasaari KM Saarela A Karihtala P Nuclear Nrf2 expression is related to a poor survival in pancreatic adenocarcinoma Pathol Res Pract 2014 210 35 9 10.1016/j.prp.2013.10.001 24189098 · DOI
- [89]Lennicke C Rahn J Lichtenfels R Wessjohann LA Seliger B Redox proteomics: Methods for the identification and enrichment of redox-modified proteins and their applications Cell Commun Signal 2015 13 39 10.1186/s12964-015-0118-6 26508685 · DOI
- [90]Li L Fath MA Scarbrough PM Watson WH Spitz DR Combined inhibition of glycolysis, the pentose cycle, and thioredoxin metabolism selectively increases cytotoxicity and oxidative stress in human breast and prostate cancer Redox Biol 2014 4C 127 35 PMC4309850 25560241
- [91]Ji X Wang H Zhu J Zhu L Pan H Li W Zhou Y Cong Z Yan F Chen S Knockdown of Nrf2 suppresses glioblastoma angiogenesis by inhibiting hypoxia-induced activation of HIF-1α Int J Cancer 2014 135 574 84 10.1002/ijc.28699 24374745 · DOI
- [92]Karki R Igwe OJ Toll-like receptor 4-mediated nuclear factor kappa B activation is essential for sensing exogenous oxidants to propagate and maintain oxidative/nitrosative cellular stress PLoS One 2013 8 e73840 10.1371/journal.pone.0073840 24058497 PMC3776800 · DOI
- [93]Gasparini C Celeghini C Monasta L Zauli G NF-kB pathways in hematological malignancies Cell Mol Life Sci 2014 71 2083 102 10.1007/s00018-013-1545-4 24419302 PMC11113378 · DOI
- [94]Yamamoto Y Gaynor RB Role of NF-kB pathway in the pathogenesois of human disease states Curr Mol Med 2001 1 287 296 10.2174/1566524013363816 11899077 · DOI
- [95]Ghosh S May MJ Kopp EB NF-kappa B and Rel proteins: evolutionarily conserved mediators of immune responses Annu Rev Immunol 1998 16 225 260 10.1146/annurev.immunol.16.1.225 9597130 · DOI
- [96]Oliveira-Marques V Marinho HS Cyrne L Antunes F Role of hydrogen peroxide in NF-kappaB activation: from inducer to modulator Antioxid Redox Signal 2009 11 2223 43 10.1089/ars.2009.2601 19496701 · DOI
- [97]Jung Y Kim H Min SH Rhee SG Jeong W Dynein light chain LC8 negatively regulates NF-kappaB through the redox-dependent interaction with IkappaBalpha J Biol Chem 2008 283 23863 71 10.1074/jbc.M803072200 18579519 PMC3259766 · DOI
- [99]Pham CG Bubici C Zazzeroni F Papa S Jones J Alvarez K Jayawardena S De Smaele E Cong R Beaumont C Torti FM Torti SV Franzoso G Ferritin heavy chain upregulation by NF-kappaB inhibits TNFalpha-induced apoptosis by suppressing reactive oxygen species Cell 2004 119 529 42 10.1016/j.cell.2004.10.017 15537542 · DOI · Paper page
- [100]Kamata H Honda S Maeda S Chang L Hirata H Karin M Reactive oxygen species promote TNF alpha-induced death and sustained JNK activation by inhibiting MAP kinase phosphatases Cell 2005 120 649 61 10.1016/j.cell.2004.12.041 15766528 · DOI · Paper page
- [102]Ma Q Kinneer K Ye J Chen BJ Inhibition of nuclear factor kappaB by phenolic antioxidants: interplay between antioxidant signaling and inflammatory cytokine expression Mol Pharmacol 2003 64 211 9 10.1124/mol.64.2.211 12869625 · DOI · Paper page
- [103]Feng X Tan W Cheng S Wang H Ye S Yu C He Y Zeng J Cen J Hu J Zheng R Zhou Y Upregulation of microRNA-126 in hepatic stellate cells may affect pathogenesis of liver fibrosis through the NF- B pathway DNA Cell Biol. 2015 34 470 80 10.1089/dna.2014.2760 25974152 · DOI
- [105]Ghashghaeinia M Toulany M Saki M Rodemann HP Mrowietz U Lang F Wieder T Potential roles of the NFkB and glutathione pathways in mature human erythrocytes Cell Mol Biol Lett 2012 17 11 20 10.2478/s11658-011-0032-x PMC6275705 22105338 · DOI
- [106]Nicola JP Peyret V Nazar M Romero JM Lucero AM Montesinos Mdel M Bocco JL Pellizas CG Masini-Repiso AM S-Nitrosylation of NF-kB p65 Inhibits TSH-Induced Na(+)/I(-) Symporter Expression Endocrinology 2015 156 4741 54 10.1210/en.2015-1192 26587909 · DOI
- [107]Shi X Dong Z Huang C Ma W Liu K Ye J Chen F Leonard SS Ding M Castranova V Vallyathan V The role of hydroxyl radical as a messenger in the activation of nuclear transcription factor NF-kappaB Mol Cell Biochem 1999 194 63 70 10.1023/A:1006904904514 10391125 · DOI
- [108]Rahman I Marwick J Kirkham P Redox modulation of chromatin remodeling: impact on histone acetylation and deacetylation, NF-kappaB and pro-inflammatory gene expression Biochem Pharmacol 2004 68 1255 67 10.1016/j.bcp.2004.05.042 15313424 · DOI · Paper page
- [109]Yamamoto Y Gaynor RB Therapeutic potential of inhibition of NF-kB pathway in the treatment of inflammation and cancer J Clin Invest 2001 107 135 142 10.1172/JCI11914 11160126 PMC199180 · DOI
- [110]Karin M Takahashi T Kapahi P Delhase M Chen Y Makris C Rothwarf D Baud V Natoli G Guido F Li N Oxidative stress and gene expression: The AP-1 and NF-kB connections Biofactors 2001 15 87 89 10.1002/biof.5520150207 12016332 · DOI · Paper page
- [112]Pinkus R Weiner LM Daniel V Role of Oxidants and Antioxidants in the Induction of AP-1, NF-kB, and Glutathione S-Transferase Gene Expression J Biol Chem 1996 271 13422 13429 10.1074/jbc.271.23.13422 8662787 · DOI
- [114]Go YM Patel RP Maland MC Park H Beckman JS Darley-Usmar VM Jo H Evidence for peroxynitrite as a signaling molecule in flow-dependent activation of c-Jun NH(2)-terminal kinase Am J Physiol 1999 277 H1647 1653 10516206
- [115]Lander HM Ogiste JS Teng KK Novogrodsky A p21 ras as a common signaling target of reactive free radicals ans cellular redox stress J Biol Chem 1995 270 21195 21198 10.1074/jbc.270.36.21195 7673152 · DOI
- [116]Nakamura H Nakamura K Yodoi J Redox regulation of cellular activation Ann Rev Immunol 1997 15 351 369 10.1146/annurev.immunol.15.1.351 9143692 · DOI
- [118]Trachootham D Lu W Ogasawara MA Valle NR Huang P Redox regulation of cell survival Antioxid Redox Signal 2008 10 1343 1374 10.1089/ars.2007.1957 18522489 PMC2932530 · DOI · Paper page
- [119]Coskun M Bjerrum JT Seidelin JB Nielsen OH MicroRNAs in inflammatory bowel disease—pathogenesis, diagnostics and therapeutics World J Gastroenterol 2012 18 4629 4634 10.3748/wjg.v18.i34.4629 23002331 PMC3442200 · DOI
- [120]Leung AKL Sharp PA MicroRNA Functions in Stress Responses Mol Cell 2010 40 205 215 10.1016/j.molcel.2010.09.027 20965416 PMC2996264 · DOI · Paper page
- [121]Lin Y Liu X Cheng Y Yang J Huo Y Zhang C Involvement of MicroRNAs in hydrogen peroxide-mediated gene regulation and cellular injury response in vascular smooth muscle cells J Biol Chem 2009 284 7903 7913 10.1074/jbc.M806920200 19158092 PMC2658083 · DOI
- [122]Wang L Huang H Fan Y Kong B Hu H Hu K Guo J Mei Y Liu W Effects of downregulation of microRNA-181a on H2O2-induced H9c2 cell apoptosis via the mitochondrial apoptotic pathway Oxid Med Cell Longev 2014 2014 1 16 PMC3942394 24683439
- [123]Christian P Su Q MicroRNA regulation of mitochondrial and ER stress signaling pathways: implications for lipoprotein metabolism in metabolic syndrome Am J Physiol—Endocrinol Metab 2014 307 E729 E737 10.1152/ajpendo.00194.2014 25184990 · DOI
- [124]Magenta A Greco S Gaetano C Martelli F Oxidative stress and microRNAs in vascular diseases Int J Mol Sci. 2013 14 17319 46 10.3390/ijms140917319 23975169 PMC3794730 · DOI
- [125]Sies H Oxidative stress: a concept in redox biology and medicine Redox Biol 2015 4 180 183 10.1016/j.redox.2015.01.002 25588755 PMC4309861 · DOI
- [126]Lopez-Bernardo E Anedda A Sánchez-Pérez P Acosta-Iborra B Cadenas S 4-Hydroxynonenal induces Nrf2-mediated UCP3 upregulation in mouse cardiomyocytes Free Radic Biol Med 2015 88 427 438 10.1016/j.freeradbiomed.2015.03.032 25843654 · DOI
- [128]den Hertog J Groen A van der Wijk T Redox regulation of protein-tyrosine phosphatases Arch Biochem Biophys 2005 434 11 15 10.1016/j.abb.2004.05.024 15629103 · DOI
- [130]Zarubin T Han J Activation and signaling of the p38 MAP kinase pathway Cell Res 2005 15 11 18 10.1038/sj.cr.7290257 15686620 · DOI
- [131]Catarzi S Romagnoli C Marcucci G Favilli F Iantomasi T Vincenzini MT Redox regulation of ERK1/2 activation induced by sphingosine 1-phosphate in fibroblasts: involvement of NADPH oxidase and platelet-derived growth factor receptor Biochim Biophys Acta 1810 2011 446 456 21256191
- [132]Meng D Shi X Jiang BH Fang J Insulin-like growth factor-I (IGF-I) induces epidermal growth factor receptor transactivation and cell proliferation through reactive oxygen species Free Radic Biol Med 2007 42 1651 1660 10.1016/j.freeradbiomed.2007.01.037 17462533 · DOI
- [133]Nagai H Noguchi T Takeda K Ichijo H Pathophysiological roles of ASK1-MAP kinase signaling pathways J Biochem Mol Biol 2007 40 1 6 10.5483/BMBRep.2007.40.1.001 17244475 · DOI
- [134]Son Y Cheong Y Kim N Chung H Kang DG Pae H Mitogen-Activated Protein Kinases and Reactive Oxygen Species: How Can ROS Activate MAPK Pathways? J Signal Transduct 2011 2011 1 6 10.1155/2011/792639 PMC3100083 21637379 · DOI · Paper page
- [135]Zhou JY Liu Y Wu GS The role of mitogen-activated protein kinase phosphatase-1 in oxidative damage-induced cell death Cancer Res 2006 66 4888 4894 10.1158/0008-5472.CAN-05-4229 16651445 · DOI
- [136]Nithianandarajah-Jones GN Wilm B Goldring CEP Müller J Cross MJ ERK5: Structure, regulation and function Cell Signal 2012 24 2187 2196 10.1016/j.cellsig.2012.07.007 22800864 · DOI
- [137]Burwell LS Nadtochıy SM Tompkins AJ Young S Brookes PS Direct evidence for S-nitrosation of mitochondrial complex I Biochem J 2006 394 627 634 10.1042/BJ20051435 16371007 PMC1383712 · DOI · Paper page
- [138]Kolesnik B Palten K Schrammel A Stessel H Schmidt K Mayer B Gorren ACF Efficient nitrosation of glutathione by nitric oxide Free Radic Biol Med 2013 63 51 64 10.1016/j.freeradbiomed.2013.04.034 23660531 PMC3734348 · DOI
- [139]Espinosa-Diez C Miguel V Mennerich D Kietzmann T Sánchez-Pérez P Cadenas S Lamas S Antioxidant responses and cellular adjustments to oxidative stress Redox Biol 2015 6 183 97 10.1016/j.redox.2015.07.008 26233704 PMC4534574 · DOI
- [140]Abello N Kerstjens HA Postma DS Bischoff R Protein tyrosine nitration: selectivity, physicochemical and biological consequences, denitration, and proteomics methods for the identification of tyrosine-nitrated proteins J Proteome Res 2009 8 3222 38 10.1021/pr900039c 19415921 · DOI · Paper page
- [141]Dröse S Brandt U Wittig I Mitochondrial respiratory chain complexes as sources and targets of thiol-based redox-regulation Biochim Biophys Acta 1844 2014 1344 1354 24561273
- [143]Glasauer A Chandel NS ROS Curr Biol 2013 23 R100 R102 10.1016/j.cub.2012.12.011 23391379 · DOI
- [144]Sena LA Chandel NS Physiological Roles of Mitochondrial Reactive Oxygen Species Mol Cell 2012 48 158 167 10.1016/j.molcel.2012.09.025 23102266 PMC3484374 · DOI · Paper page
- [145]Finkel T Signal transduction by mitochondrial oxidants J Biol Chem 2012 287 4434 4440 10.1074/jbc.R111.271999 21832045 PMC3281633 · DOI · Paper page
- [146]Yun J Finkel T Mitohormesis Cell Metab 2014 19 757 766 10.1016/j.cmet.2014.01.011 24561260 PMC4016106 · DOI · Paper page
- [147]Rahman K Studies on free radicals, antioxidants, and co-factors Clin Interv Aging 2007 2 219 36 18044138 PMC2684512
- [148]Molavian H Tonekaboni AM Kohandel M Sivaloganathan S The Synergetic Coupling among the Cellular Antioxidants Glutathione Peroxidase/Peroxiredoxin and Other Antioxidants and its Effect on the Concentration of H2O2 Sci Rep 2015 5 1 8 10.1038/srep13620 · DOI
- [149]Sheng Y Abreu IA Cabelli DE Maroney MJ Miller A Teixeira M Valentine JS Superoxide Dismutases and Superoxide Reductases Chem Rev 2014 114 3854 3918 10.1021/cr4005296 24684599 PMC4317059 · DOI · Paper page
- [150]Schmölz L Birringer M Lorkowski S Wallert M Complexity of vitamin E metabolism World J Biol Chem 2016 7 14 43 10.4331/wjbc.v7.i1.14 26981194 PMC4768118 · DOI
- [151]Singh U Devaraj S Jialal I Vitamın E, oxidative stress, and inflammation Ann Rev Nutr 2005 25 151 174 10.1146/annurev.nutr.24.012003.132446 16011463 · DOI
- [152]Wang X Quinn PJ The location and function of vitamin E in membranes (review) Mol Membr Biol 2000 17 143 56 10.1080/09687680010000311 11128973 · DOI
- [153]Kojo S Vitamin C: basic metabolism and its function as an index of oxidative stress Curr Med Chem 2004 11 1041 1064 10.2174/0929867043455567 15078165 · DOI
- [154]Birk J Meyer M Aller I Hansen HG Odermatt A Dick TP Meyer AJ Appenzeller-Herzog C Endoplasmic reticulum: reduced and oxidized glutathione revisited J Cell Sci 2013 126 1604 17 10.1242/jcs.117218 23424194 · DOI
- [155]Bharath S Hsu M Kaur D Rajagopalan S Andersen JK Glutathione, iron and Parkinson’s disease Biochem Pharmacol 2002 64 1037 1048 10.1016/S0006-2952(02)01174-7 12213603 · DOI
- [156]Warner DS Sheng H Batinic’-Haberle I Oxidants, antioxidants and the ischemic brain J Exp Biol 2004 207 3221 3231 10.1242/jeb.01022 15299043 · DOI
- [157]Pastore A Federici G Bertini E Piemonte F Analysis of glutathione: implication in redox and detoxification Clin Chim Acta 2003 333 19 39 10.1016/S0009-8981(03)00200-6 12809732 · DOI
- [158]Mills BJ Weiss MM Lang CA Liu MC Ziegler C Blood glutathione and cysteine changes in cardiovascular disease J Lab Clin Med 2000 135 396 402 10.1067/mlc.2000.105976 10811054 · DOI
- [159]Navarro J Obrador E Carretero J Petschen I Aviñó J Perez P Estrela JM Changes in glutathione status and the antioxidant system in blood and in cancer cells associate with tumour growth in vivo Free Radic Biol Med 1999 26 410 418 10.1016/S0891-5849(98)00213-5 9895233 · DOI
- [160]Rubartelli A Bonifaci N Sitia R High rates of thioredoxin secretion correlate with growth arrest in hepatoma cells Cancer Res 1995 55 675 680 7834639
- [161]Tonissen KF Di Trapani G Thioredoxin system inhibitors as mediators of apoptosis for cancer therapy Mol Nutr Food Res 2009 53 87 103 10.1002/mnfr.200700492 18979503 · DOI
- [162]Yoshida S Katoh T Tetsuka T Uno K Matsui N Okamoto T Involvement of thioredoxin in rheumatoid arthritis: its costimulatory roles in the TNF-alpha-induced production of IL-6 and IL-8 from cultured synovial fibroblasts J Immunol 1999 163 351 358 10384135
- [163]Nakamura H De Rosa S Roederer M Anderson MT Dubs JG Yodoi J Holmgren A Herzenberg LA Herzenberg LA Elevation of plasma thioredoxin levels in HIV-infected individuals Int Immunol 1996 8 603 611 10.1093/intimm/8.4.603 8671648 · DOI
- [164]Packer L Roy S Sen CK Alpha-lipoic acid: a metabolic antioxidant and potential redox modulator of transcription Adv Pharmacol 1997 38 79 101 10.1016/S1054-3589(08)60980-1 8895805 · DOI
- [165]Senoglu M Nacitarhan V Kurutas EB Senoglu N Altun I Atli Y Ozbag D Intraperitoneal alpha-lipoic acid to prevent neural damage after crush injury to the rat sciatic nerve J Brachial Plex Peripher Nerve Inj 2009 4 22 27 19939272 PMC2789059
- [167]Knight TR Fariss MW Farhood A Jaeschke H Role of lipid peroxidation as a mechanism of liver injury after acetaminophen overdose in mice Toxicol Sci 2003 6 229 236 10.1093/toxsci/kfg220 12944590 · DOI
- [168]Bajt ML Knight TR Lemasters JJ Jaeschke H Acetaminophen-induced oxidant stress and cell injury in cultured Mouse hepatocytes: Protection by N-acetyl cysteine Toxicol Sci 2004 80 343 349 10.1093/toxsci/kfh151 15115886 · DOI
- [169]Brener PH Ballardo M Mariani G Cernadas JMC Medication error in an extremely low birth weight newborn: Paracetamol overdose Arch Argent Pediatr 2013 111 53 5 23381705
- [170]Cetinkaya A Bulbuloglu E Belge Kurutas E Ciralik H Kantarceken B Buyukbese MA Beneficial effects of n-acetylcysteine on acetic acid-induced colitis in rats Tohoku J Exp Med 2005 206 131 139 10.1620/tjem.206.131 15888969 · DOI
- [171]Reiter RJ Acuña-Castroviejo D Tan DX Burkhardt S Free radical-mediated molecular damage. Mechanisms for the protective actions of melatonin in the central nervous system Ann N Y Acad Sci 2001 939 200 215 10.1111/j.1749-6632.2001.tb03627.x 11462772 · DOI
- [174]Mahima RA Deb R Latheef SK Abdul Samad H Tiwari R Verma AK Kumar A Dhama K Immunomodulatory and therapeutic potentials of herbal, traditional/indeginous and ethnoveterinary medicines Pak J Biol Sci 2012 15 754 774 10.3923/pjbs.2012.754.774 24175417 · DOI
- [175]Joshipura KJ Ascherio A Manson JE Stampfer MJ Rimm EB Speizer FE Hennekens CH Spiegelman D Willett WC Fruit and vegetable intake in relation to risk of ischemic stroke JAMA 1999 282 12331 1239 10.1001/jama.282.13.1233 10517425 · DOI · Paper page
- [176]Cox BD Whichelow MJ Prevost AT Seasonal consumption of salad vegetables and fresh fruit in relation to the development of cardiovascular disease and cancer Public Health Nutr 2000 3 19 29 10.1017/S1368980000000045 10786720 · DOI
- [177]Eastwood MA Interaction of dietary antioxidants in vivo: how fruit and vegetables prevent disease? QJM 1999 92 527 530 10.1093/qjmed/92.9.527 10627873 · DOI
- [179]Gilgun-Sherki Y Melamed E Offen D Antioxidant treatment in Alzheimer’s disease: current state J Mol Neurosci 2003 21 1 11 10.1385/JMN:21:1:1 14500988 · DOI
- [180]Altun I Kurutas EB G Protein-Coupled Estrogen Receptor Levels After Peripheral Nerve Injury in an Experimental Rat Model World Neurosurg 2015 84 1903 1906 10.1016/j.wneu.2015.08.028 26325209 · DOI
- [181]Vivekananthan DP Penn MS Sapp SK Hsu A Topol EJ Use of antioxidant vitamins for the prevention of cardiovascular disease: meta-analysis of randomised trials Lancet 2003 361 2017 2023 10.1016/S0140-6736(03)13637-9 12814711 · DOI · Paper page
- [182]Belge Kurutas E Senoglu M Yuksel KZ Unsal V Altun I Oxidative/Nitrosative Stress in Patients With Modic Changes: Preliminary Controlled Study Spine (Phila Pa 1976) 2015 40 1101 1107 10.1097/BRS.0000000000000737 25494311 · DOI
- [183]Block KI Koch AC Mead MN Tothy PK Newman RA Gyllenhaal C Impact of antioxidant supplementation on chemotherapeutic efficacy: A systematic review of the evidence from randomized controlled trials Cancer Treat Rev 2007 33 407 418 10.1016/j.ctrv.2007.01.005 17367938 · DOI
- [184]Conklin KA Chemotherapy-associated oxidative stress: impact on chemotherapeutic effectiveness Integr Cancer Ther 2004 3 294 300 10.1177/1534735404270335 15523100 · DOI · Paper page
- [185]Lawenda BD Kelly KM Ladas EJ Sagar SM Vickers A Blumberg JB Should Supplemental antioxidant administration be avoided during chemotherapy and radiation therapy? J Natl Cancer Inst 2008 100 773 783 10.1093/jnci/djn148 18505970 · DOI
- [186]Hrelia S Bordoni A Angeloni C Leoncini E Biagi P Nutritional interventions to counteract oxidative stress in cardiac cells Ital J Biochem 2004 53 157 63 15997908
- [187]Niki E Antioxidants: Basic Principles, Emerging Concepts, and Problems Biomed J 2014 37 106 111 24923567
- [188]Niki E Do antioxidants impair signaling by reactive oxygen species and lipid oxidation products? FEBS Lett 2012 586 3767 3770 10.1016/j.febslet.2012.09.025 23022561 · DOI
- [189]Rahal A Kumar A Singh V Yadav B Tiwari R Chakraborty S Dhama K Oxidative stress, prooxidants, and antioxidants: the interplay BioMed Res Int 2014 2014 1 19 10.1155/2014/761264 PMC3920909 24587990 · DOI
- [191]Buettner GR Jurkiewicz BA Catalytic metals, ascorbate and free radicals: combinations to avoid Rad Res 1996 145 532 541 10.2307/3579271 8619018 · DOI
- [193]Yao HT Luo MN Hung LB Chiang MT Lin JH Lii CK Huang CY Effects of chitosan oligosaccharides on drug-metabolizing enzymes in rat liver and kidneys Food Chem Toxicol 2012 50 1171 7 10.1016/j.fct.2012.02.022 22386817 · DOI
- [194]Hebbar V Shen G Hu R Kim BR Chen C Korytko PJ Crowell JA Levine BS Kong AN Toxicogenomics of resveratrol in rat liver Life Sci 2005 76 2299 314 10.1016/j.lfs.2004.10.039 15748624 · DOI
- [196]Kontush A Finckh B Karten B Kohlsch¨utter A Beisiegel U Antioxidant and prooxidant activity of α-tocopherol in human plasma and low density lipoprotein J Lipid Res 1996 37 1436 1448 8827516
- [197]Halliwell B Are polyphenols antioxidants or pro-oxidants? What do we learn from cell culture and in vivo studies? Arch Biochem Biophys 2008 476 107 112 10.1016/j.abb.2008.01.028 18284912 · DOI
- Authors
- Kurutas, E. B.
- Venue
- Nutrition Journal
- Published
- 2015-12
- Volume
- 15
- Issue
- 1
- Pages
- 71-71
- ISSN
- 1475-2891 (ISSN-L)
- PMC
- PMC4960740
- OpenAlex
- W2485662396
- Cited by
- 2,152
- References
- 209
- Citations by year
- 2026: 92 · 2025: 193 · 2024: 249 · 2023: 326 · 2022: 385 · 2021: 376 · 2020: 330 · 2019: 116 · 2018: 56 · 2017: 22 · 2016: 5 · 2013: 1
- FWCI
- 2.90
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Nutrition Journal (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Health Sciences › Medicine › Biochemistry › Phytochemicals and Antioxidant Activities
- Keywords
- antioxidants, oxidative stress, nitrosative stress, reactive oxygen species, reactive nitrogen species, lipid peroxidation, malondialdehyde, 4-hydroxynonenal, acrolein, isoprostanes, free radical scavenging, antioxidant supplementation, pro-oxidant activity, antioxidant deficiency, redox conditions
- MeSH terms
- Antioxidants, Gene Expression Regulation, Humans, Protein Kinases, Transcription Factors, Lipid Peroxidation, Randomized Controlled Trials as Topic, Protein Tyrosine Phosphatases, Reactive Oxygen Species, Oxidative Stress, Dietary Supplements, Reactive Nitrogen Species
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