Oxidative stress, prooxidants, and antioxidants: The interplay

BioMed Research International

Volumn 2014, Issue , 2014, Pages

  Rahal, Anu ^a   Kumar, Amit ^a   Singh, Vivek ^a   Yadav, Brijesh ^a   Tiwari, Ruchi ^a   Chakraborty, Sandip ^b   Dhama, Kuldeep ^c  

^a Deen Dayal Upadhayay Pashu Chikitsa Vigyan Vishwa Vidyalaya Evam Go Anusandhan Sansthan ^*  (India)

^b Animal Resources Development Department   (India)

^c INDIAN VETERINARY RESEARCH INSTITUTE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIOXIDANT; REACTIVE NITROGEN SPECIES; REACTIVE OXYGEN METABOLITE;

GENETICS; HUMAN; METABOLISM; OXIDATION REDUCTION REACTION; OXIDATIVE STRESS; REVIEW;

ANTIOXIDANTS; HUMANS; OXIDATION-REDUCTION; OXIDATIVE STRESS; REACTIVE NITROGEN SPECIES; REACTIVE OXYGEN SPECIES;

EID: 84893744320     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2014/761264     Document Type: Review

References (215)

1. Kumar A., Rahal A., Diwedi S. K., Gupta M. K., Bacterial prevalence and antibiotic resistance profile from bovine mastitis in Mathura, India. Egyptian Journal of Dairy Sciences 2010 38 1 31 34
2. Kumar A., Rahal A., Verma A. K., In-Vitro antibacterial activity of hot aqueous extract (HAE) of Ocimum sanctum (Tulsi) leaves. Indian Journal of Veterinary Medicine 2011 36 2 75 76
3. McGinnis J. M., Foege W. H., Actual causes of death in the United States. Journal of the American Medical Association 1993 270 18 2207 2212 2-s2.0-0027360855 10.1001/jama.270.18.2207 (Pubitemid 23323637)
4. Mahima, Rahal A., Deb R., Latheef S. K., Samad H. A., Tiwari R., Verma A. K., Kumar A., Dhama K., Immunomodulatory and therapeutic potentials of herbal, traditional/indeginous and ethnoveterinary medicines. Pakistan Journal of Biological Sciences 2012 15 16 754 774 10.3923/pjbs.2012.754.774
5. Ahmad A. H., Rahal A., Tripathi A., Optimising drug potential of plants. Proceedings of the 6th Annual Conference of the Recent Trends in Development of Herbal Drugs: Challenges and Opportunities (ISVPT '06) 2006 Bihar, India 23 25
6. Ahmad A. H., Rahal A., Siddiqui N., Bioprospecting of medicinal plants. Proceedings of the National Conference on Increasing Production and Productivity of Medicinal and Aromatic Plants Through Traditional Practices September 2008 Uttrakhand, India Department of Plant Pathology, College of Agriculture, GBPUA&T
7. Gillman M. W., Cupples L. A., Gagnon D., Posner B. M., Ellison R. C., Castelli W. P., Wolf P. A., Protective effect of fruits and vegetables on development of stroke in men. Journal of the American Medical Association 1995 273 14 1113 1117 2-s2.0-0028920708
8. Joshipura K. J., Ascherio A., Manson J. E., Stampfer M. J., Rimm E. B., Speizer F. E., Hennekens C. H., Spiegelman D., Willett W. C., Fruit and vegetable intake in relation to risk of ischemic stroke. Journal of the American Medical Association 1999 282 13 1233 1239 2-s2.0-0033530268 10.1001/jama.282.13.1233 (Pubitemid 29468494)
9. Cox B. D., Whichelow M. J., Prevost A. T., Seasonal consumption of salad vegetables and fresh fruit in relation to the development of cardiovascular disease and cancer. Public Health Nutrition 2000 3 1 19 29 2-s2.0-0034004047 (Pubitemid 30214554)
10. Strandhagen E., Hansson P.-O., Bosaeus I., Isaksson B., Eriksson H., High fruit intake may reduce mortality among middle-aged and elderly men. The study of men born in 1913. European Journal of Clinical Nutrition 2000 54 4 337 341 2-s2.0-0034109048 10.1038/sj.ejcn.1600959 (Pubitemid 30201453)
11. Eastwood M. A., Interaction of dietary antioxidants in vivo: how fruit and vegetables prevent disease? QJM 1999 92 9 527 530 2-s2.0-0032824007 (Pubitemid 29430051)
12. Rahal A., Ahmad A. H., Kumar A., Mahima, Verma A. K., Chakraborty S., Dhama K., Clinical drug interactions: a holistic view. Pakistan Journal of Biological Sciences 2013 16 16 751 758
13. Potter J. D., Cancer prevention: epidemiology and experiment. Cancer Letters 1997 114 1-2 7 9 2-s2.0-0030932381 10.1016/S0304-3835(97)04615-6 (Pubitemid 27140065)
14. Dimitrios N. T., Geogrios K. C., Dmitrios I. X. H., Neurohormonal hypothesis in heart failure. Hellenic Journal of Cardiology 2003 44 3 195 205 2-s2.0-0842333822
15. Lundgren K., Kalev K., Chuansi G. A. O., Ingvar H., Effects of heat stress on working populations when facing climate change. Industrial Health 2013 51 3 15 10.2486/indhealth.2012-0089
16. Kock M. D., Jessup D. A., Clark R. K., Franti C. E., Effects of capture on biological parameters in free-ranging bighorn sheep (Ovis canadensis): evaluation of drop-net, drive-net, chemical immobilization and the net-gun. Journal of Wildlife Diseases 1987 23 4 641 651 2-s2.0-0023424549
17. Hoult J. R. S., Moroney M. A., Paya M., Actions of flavonoids and coumarins on lipoxygenase and cyclooxygenase. Methods in Enzymology 1994 234 443 454 2-s2.0-0027973797 10.1016/0076-6879(94)34115-X
18. Akhalaya M. Y., Platonov A. G., Baizhumanov A. A., Short-term cold exposure improves antioxidant status and general resistance of animals. Bulletin of Experimental Biology and Medicine 2006 141 1 26 29 2-s2.0-33745065537 10.1007/s10517-006-0084-5 (Pubitemid 43880499)
19. Kock M. D., Clark R. K., Franti C. E., Jessup D. A., Wehausen J. D., Effects of capture on biological parameters in free-ranging bighorn sheep (Ovis canadensis): evaluation of normal, stressed and mortality outcomes and documentation of postcapture survival. Journal of Wildlife Diseases 1987 23 4 652 662 2-s2.0-0023427014
20. Ziegler R., Changes in lipid and carbohydrate metabolism during starvation in adult Manduca sexta. Journal of Comparative Physiology B 1991 161 2 125 131 2-s2.0-0025986213 10.1007/BF00262874
21. Golikov N., Adaptation in Farm Animals 1985 Sofia, Bulgaria Agropromizdat
22. Pekow C., Defining, measuring, and interpreting stress in laboratory animals. Contemporary Topics in Laboratory Animal Science 2005 44 2 41 45 2-s2.0-17144365473 (Pubitemid 41542234)
23. Trachootham D., Lu W., Ogasawara M. A., Valle N. R., Huang P., Redox regulation of cell survival. Antioxidants and Redox Signaling 2008 10 8 1343 1374 2-s2.0-51749088156 10.1089/ars.2007.1957
24. Dhanalakshmi S., Srikumar R., Manikandan S., Parthasarathy N. J., Devi R. S., Antioxidant property of triphala on cold stress induced oxidative stress in experimental rats. Journal of Health Science 2006 52 6 843 847 2-s2.0-33845386343 10.1248/jhs.52.843 (Pubitemid 44903960)
25. Rahal A., Singh V., Mehra D., Rajesh S., Ahmad A. H., Prophylactic efficacy of Podophyllum hexandrum in alleviation of immobilization stress induced oxidative damage in rats. Journal of Natural Products 2009 2 110 115
26. Lishmanov I., Lasukova T. V., Afanas'ev S. A., Maslov L. N., Krotenko N. M., Naryzhnaia N. V., Effect of cold stress on the contractile activity, carbohydrate and energy metabolism in the isolated rat heart. Patologicheskaia Fiziologiia i èksperimental'naia Terapiia 1997 1 28 31 2-s2.0-0030628846
27. Gurin V. N., Lapsha V. I., Streletskaia L. G., Changes in the catecholamine level and energy metabolism of the myocardium in rats during cold and emotional stress. Fiziologicheskii zhurnal SSSR imeni I. M. Sechenova 1989 75 4 542 547 2-s2.0-0024643995
28. Afanas'ev S. A., Kondrat'ev B. I., Alekseeva E. D., Lishmanov I. B., Effect of the acute exposure to cold on the heart muscle. Rossiiskii Fiziologicheskii Zhurnal imeni I.M. Sechenova 1997 83 4 98 102 2-s2.0-0031107187
29. Powers S. K., Jackson M. J., Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production. Physiological Reviews 2008 88 4 1243 1276 2-s2.0-55949118714 10.1152/physrev.00031.2007
30. Vina J., Borras C., Gomez-Cabrera M., Orr W. C., Part of the series: from dietary antioxidants to regulators in cellular signalling and gene expression. Role of reactive oxygen species and (phyto)oestrogens in the modulation of adaptive response to stress. Free Radical Research 2006 40 2 111 119 2-s2.0-30144442994 10.1080/10715760500405778 (Pubitemid 43050872)
31. Powers S. K., Criswell D., Lawler J., Li Li Ji L. L. J., Martin D., Herb R. A., Dudley G., Influence of exercise and fiber type on antioxidant enzyme activity in rat skeletal muscle. American Journal of Physiology 1994 266 2 R375 R380 2-s2.0-0028331680
32. Powers S. K., Criswell D., Lawler J., Martin D., Li Li Ji L. L. J., Herb R. A., Dudley G., Regional training-induced alterations in diaphragmatic oxidative and antioxidant enzymes. Respiration Physiology 1994 95 2 227 237 2-s2.0-0028040217 10.1016/0034-5687(94)90118-X (Pubitemid 24066433)
33. Gomez-Cabrera M. C., Domenech E., Viña J., Moderate exercise is an antioxidant: upregulation of antioxidant genes by training. Free Radical Biology and Medicine 2008 44 2 126 131 2-s2.0-37849021505 10.1016/j.freeradbiomed.2007. 02.001
34. Wood G. E., Norris E. H., Waters E., Stoldt J. T., McEwen B. S., Chronic immobilization stress alters aspects of emotionality and associative learning in the rat. Behavioral Neuroscience 2008 122 2 282 292 2-s2.0-43449113531 10.1037/0735-7044.122.2.282 (Pubitemid 351672320)
35. Castagliuolo I., LaMont J. T., Qiu B., Fleming S. M., Bhaskar K. R., Nikulasson S. T., Kornetsky C., Pothoulakis C., Acute stress causes mucin release from rat colon: role of corticotropin releasing factor and mast cells. American Journal of Physiology 1996 271 5 G884 G892 2-s2.0-0029811284
36. Ceccatelli S., Eriksson M., Hokfelt T., Distribution and coexistence of corticotropin-releasing factor-, neurotensin-, enkephalin-, cholecystokinin-, galanin- and vasoactive intestinal polypeptide/peptide histidine isoleucine-like peptides in the parvocellular part of the paraventricular nucleus. Neuroendocrinology 1989 49 3 309 323 2-s2.0-0024498644 (Pubitemid 19095272)
37. Augeron C., Voisin T., Maoret J. J., Berthon B., Laburthe M., Laboisse C. L., Neurotensin and neuromedin N stimulate mucin output from human goblet cells (Cl.16E) via neurotensin receptors. American Journal of Physiology 1992 262 3 G470 G476 2-s2.0-0026528664
38. Sandner N., Stangassinger M., Giesecke D., The effect of glucocorticoid on the glucose metabolism of pigmy goats. 1. Selected metabolites of energy metabolism. Zentralblatt fur Veterinarmedizin A 1990 37 1 35 44 2-s2.0-0025379252
39. Duhault J., Lacour F., Espinal J., Rolland Y., Effect of activation of the serotoninergic system during prolonged starvation on subsequent caloric intake and macronutrient selection in the Zucker rat. Appetite 1993 20 2 135 144 2-s2.0-0027193320 10.1006/appe.1993.1015 (Pubitemid 23165580)
40. Ohama T., Matsuki N., Saito H., Tsukamoto K., Kinoshita M., Katsuragawa K., Okazaki S., Yamanaka M., Teramoto T., Effect of starving and refeeding on lipid metabolism in suncus. Journal of Biochemistry 1994 115 2 190 193 2-s2.0-0027977773 (Pubitemid 24060146)
41. Munch I. C., Influences of time intervals between meals and total food intake on resting metabolic rate in rats. Acta Physiologica Scandinavica 1995 153 3 243 247 2-s2.0-0028945248
42. Chung H. C., Sung S. H., Kim J. S., Kim Y. C., Kim S. G., Lack of cytochrome P450 2E1 (CYP2E1) induction in the rat liver by starvation without coprophagy. Drug Metabolism and Disposition 2001 29 3 213 216 2-s2.0-0035115015
43. Shi D., Xie F., Zhai C., Stern J. S., Liu Y., Liu S., The role of cellular oxidative stress in regulating glycolysis energy metabolism in hepatoma cells. Molecular Cancer 2009 8 32 2-s2.0-67650085650 10.1186/1476-4598-8-32
44. Potter E. L., Dehority B. A., Effects of changes in feed level, starvation, and level of feed after starvation upon the concentration of rumen protozoa in the ovine. Applied Microbiology 1973 26 5 692 698 2-s2.0-0015688477
45. Burxer G. V., Stress in farm animals. Veterinaria 1974 8 92 94
46. Peng H., Coon M. J., Regulation of rabbit cytochrome P450 2E1 expression in HepG2 cells by insulin and thyroid hormone. Molecular Pharmacology 1998 54 4 740 747 2-s2.0-0031756902 (Pubitemid 28480978)
47. Yamazoe Y., Murayama N., Shimada M., Yamauchi K., Kato R., Cytochrome P450 in livers of diabetic rats: regulation by growth hormone and insulin. Archives of Biochemistry and Biophysics 1989 268 2 567 575 2-s2.0-0024559080 (Pubitemid 19049735)
48. Son M. H., Kang K. W., Kim E. J., Ryu J. H., Cho H., Kim S. H., Kim W. B., Kim S. G., Role of glucose utilization in the restoration of hypophysectomy-induced hepatic cytochrome P450 2E1 by growth hormone in rats. Chemico-Biological Interactions 2000 127 1 13 28 2-s2.0-0343090856 10.1016/S0009-2797(00)00166-6 (Pubitemid 30618729)
49. Sinsch U., Seine R., Sherif N., Seasonal changes in the tolerance of osmotic stress in natterjack toads (Bufo calamita). Comparative Biochemistry and Physiology 1992 101 2 353 360 2-s2.0-0026573318 10.1016/0300-9629(92)90546-3
50. Liu Y., Fiskum G., Schubert D., Generation of reactive oxygen species by the mitochondrial electron transport chain. Journal of Neurochemistry 2002 80 5 780 787 2-s2.0-0036319021 10.1046/j.0022-3042.2002.00744.x (Pubitemid 34809230)
51. Freisleben H. J., Kriege H., Clarke C., Beyersdorf F., Zimmer G., Hemodynamic and mitochondrial parameters during hypoxia and reoxygenation in working rat hearts. Arzneimittel-Forschung 1991 41 1 81 88 2-s2.0-0026088720
52. Feuvray D., James F., De Leiris J., Protective effect of endogenous catecholamine depletion against hypoxic and reoxygenation damage in isolated rat heart: an ultrastructural study. Journal de Physiologie 1980 76 7 717 722 2-s2.0-0019132121 (Pubitemid 11197444)
53. Poli G., Leonarduzzi G., Biasi F., Chiarpotto E., Oxidative stress and cell signalling. Current Medicinal Chemistry 2004 11 9 1163 1182 2-s2.0-2342629352 (Pubitemid 38585060)
54. Sohal R. S., Role of oxidative stress and protein oxidation in the aging process. Free Radical Biology and Medicine 2002 33 1 37 44 2-s2.0-0036628724 10.1016/S0891-5849(02)00856-0 (Pubitemid 34681004)
55. Ahmed A. D., Hye-Yeon C., Jung-Hyun K., Ssang-Goo C., Role of oxidative stress in stem, cancer, and cancer stem cells. Cancers 2010 2 2 859 884 2-s2.0-79952256467 10.3390/cancers2020859
56. Valko M., Rhodes C. J., Moncol J., Izakovic M., Mazur M., Free radicals, metals and antioxidants in oxidative stress-induced cancer. Chemico-Biological Interactions 2006 160 1 1 40 2-s2.0-32444433202 10.1016/j.cbi.2005.12.009 (Pubitemid 43227479)
57. Inoue M., Sato E. F., Nishikawa M., Park A., Kira Y., Imada I., Utsumi K., Mitochondrial generation of reactive oxygen species and its role in aerobic life. Current Medicinal Chemistry 2003 10 23 2495 2505 2-s2.0-0344513852 10.2174/0929867033456477 (Pubitemid 37460972)
58. Parke D. V., Sapota A., Chemical toxicity and reactive oxygen species. International Journal of Occupational Medicine and Environmental Health 1996 9 4 331 340 2-s2.0-0030455158 (Pubitemid 27075202)
59. Misra H. P., Fridovich I., The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. Journal of Biological Chemistry 1972 247 10 3170 3175 2-s2.0-0015523099
60. Reed D. J., De Matteis F., Smith L. L., Toxicity of oxygen. Molecular and Cellular Mechanisms of Toxicity 1995 Boca Raton, Fla, USA CRC Press 35 68
61. Yu B. P., Cellular defenses against damage from reactive oxygen species. Physiological Reviews 1994 74 1 139 162 2-s2.0-0010471495 (Pubitemid 24045676)
62. Stoian I., Oros A., Moldoveanu E., Apoptosis and free radicals. Biochemical and Molecular Medicine 1996 59 2 93 97 2-s2.0-0030445935 10.1006/bmme.1996.0072 (Pubitemid 27036496)
63. Younes M., Free radicals and reactive oxygen species, in toxicology, 'By H. Marguardt, Mechanisms of antioxidant and pro-oxidant effects of lipoic acid in the diabetic and nondiabetic kidney'. Kidney International 1999 67 4 1371 1380
64. Marks D. B., Marks A. D., Smith C. M., Oxygen metabolism and toxicityin. Basic Medical Biochemistry: A Clinical Approach 1996 Baltimore, Md, USA Williams and Wilkins 327 340
65. Tak P. P., Firestein G. S., NF- B: a key role in inflammatory diseases. Journal of Clinical Investigation 2001 107 1 7 11 2-s2.0-0034746919
66. Aw Tak T., Molecular and cellular responses to oxidative stress and changes in oxidation-reduction imbalance in the intestine. American Journal of Clinical Nutrition 1999 70 4 557 565 2-s2.0-0000092645
67. Rhee S. G., Bae Y. S., Lee S. R., Kwon J., Hydrogen peroxide: a key messenger that modulates protein phosphorylation through cysteine oxidation. Science STKE 2000 10 53 1 2-s2.0-0034633602
68. Liu X., Kim C. N., Yang J., Jemmerson R., Wang X., Induction of apoptotic program in cell-free extracts: requirement for dATP and cytochrome c. Cell 1996 86 1 147 157 2-s2.0-0030581151 10.1016/S0092-8674(00)80085-9 (Pubitemid 26256586)
69. Pryor W. A., Houk K. N., Foote C. S., Fukuto J. M., Ignarro L. J., Squadrito G. L., Davies K. J. A., Free radical biology and medicine: it's a gas, man! American Journal of Physiology 2006 291 3 R491 R511 2-s2.0-33746833881 10.1152/ajpregu.00614.2005 (Pubitemid 44352329)
70. Olszanecki R., Gbska A., Kozlovski V. I., Gryglewski R. J., Flavonoids and nitric oxide synthase. Journal of Physiology and Pharmacology 2002 53 4 571 584 2-s2.0-0036912465 (Pubitemid 36014803)
71. Pavanato A., Tuñón M. J., Sánchez-Campos S., Marroni C. A., Llesuy S., González-Gallego J., Effects of quercetin on liver damage in rats with carbon tetrachloride-induced cirrhosis. Digestive Diseases and Sciences 2003 48 4 824 829 2-s2.0-0344642984 10.1023/A:1022869716643 (Pubitemid 36390692)
72. Miyamoto M., Hashimoto K., Minagawa K., Satoh K., Komatsu N., Fujimaki M., Nakashima H., Yokote Y., Akahane K., Guputa M., Sarma D. N. K., Mitra S. K., Sakagami H., Effect of poly-herbal formula on NO production by LPS-stimulated mouse macrophage-like cells. Anticancer Research A 2002 22 6 3293 3301 2-s2.0-0036871216 (Pubitemid 36070105)
73. Akyol O., Zoroglu S., Armutcu F., Sahin S., Gurel A., Nitric oxide as a physiopathological factor in neuropsychiatric disorders. In Vivo 2004 18 3 377 390 2-s2.0-4043106393 (Pubitemid 39069754)
74. Halliwell B., Whiteman M., Measuring reactive species and oxidative damage in vivo and in cell culture: how should you do it and what do the results mean? British Journal of Pharmacology 2004 142 2 231 255 2-s2.0-2942572700 10.1038/sj.bjp.0705776 (Pubitemid 38746160)
75. Knott A. B., Bossy-Wetzel E., Nitric oxide in health and disease of the nervous system. Antioxidants and Redox Signaling 2009 11 3 541 553 2-s2.0-58849147441 10.1089/ars.2008.2234
76. Marnett L. J., Oxyradicals and DNA damage. Carcinogenesis 2000 21 3 361 370 2-s2.0-0034011261 (Pubitemid 30137921)
77. von Schantz T., Bensch S., Grahn M., Hasselquist D., Wittzell H., Good genes, oxidative stress and condition-dependent sexual signals. Proceedings of the Royal Society B 1999 266 1414 1 12 2-s2.0-0033531228 10.1098/rspb.1999.0597 (Pubitemid 29039269)
78. Costantini D., Oxidative stress in ecology and evolution: lessons from avian studies. Ecology Letters 2008 11 11 1238 1251 2-s2.0-55949127435 10.1111/j.1461-0248.2008.01246.x
79. Monaghan P., Metcalfe N. B., Torres R., Oxidative stress as a mediator of life history trade-offs: mechanisms, measurements and interpretation. Ecology Letters 2009 12 1 75 92 2-s2.0-57549116867 10.1111/j.1461-0248.2008.01258.x
80. Halliwell B., Gutteridge J. M. C., Free Radicals in Biology and Medicine 2007 3rd Oxford, UK Oxford University Press
81. Ďuračková Z., Bergendi Ľ., Čársky J., Free Radicals and Antioxidants in Medicine (II) 1999 Bratislava, Slovakia SAP
82. Klimp A. H., De Vries E. G. E., Scherphof G. L., Daemen T., A potential role of macrophage activation in the treatment of cancer. Critical Reviews in Oncology and Hematology 2002 44 2 143 161 2-s2.0-12244260787 10.1016/S1040-8428(01)00203-7 (Pubitemid 36159043)
83. Ďuračková Z., Some current insights into oxidative stress. Physiological Research 2010 59 4 459 469 2-s2.0-77958114712
84. Forman H., Maiorino M., Ursini F., Signaling functions of reactive oxygen species. Biochemistry 2010 49 5 835 842 2-s2.0-75749136883 10.1021/bi9020378
85. Bienert G. P., Møller A. L. B., Kristiansen K. A., Schulz A., Møller I. M., Schjoerring J. K., Jahn T. P., Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranes. Journal of Biological Chemistry 2007 282 2 1183 1192 2-s2.0-33847753534 10.1074/jbc.M603761200 (Pubitemid 47076557)
86. 2 permeation through cytoplasmic and peroxisomal membranes: comparison with experimental data. Biochimica et Biophysica Acta 2004 1673 3 149 159 2-s2.0-3242774397 10.1016/j.bbagen.2004.04. 011 (Pubitemid 38981768)
87. Nisticò R., Piccirilli S., Cucchiaroni M. L., Armogida M., Guatteo E., Giampà C., Fusco F. R., Bernardi G., Nisticò G., Mercuri N. B., Neuroprotective effect of hydrogen peroxide on an in vitro model of brain ischaemia. British Journal of Pharmacology 2008 153 5 1022 1029 2-s2.0-40149087718 10.1038/sj.bjp.0707587 (Pubitemid 351328932)
88. Finkel T., Oxygen radicals and signaling. Current Opinion in Cell Biology 1998 10 2 248 253 2-s2.0-0032053707 10.1016/S0955-0674(98)80147-6 (Pubitemid 28174767)
89. Tonks N. K., Redox redux: revisiting PTPs and the control of cell signaling. Cell 2005 121 5 667 670 2-s2.0-20444400257 10.1016/j.cell.2005.05.016 (Pubitemid 40797589)
90. Kovacic P., Jacintho J. D., Mechanisms of carcinogenesis: focus on oxidative stress and electron transfer. Current Medicinal Chemistry 2001 8 7 773 796 2-s2.0-0035025124 (Pubitemid 32427906)
91. Ridnour L. A., Isenberg J. S., Espey M. G., Thomas D. D., Roberts D. D., Wink D. A., Nitric oxide regulates angiogenesis through a functional switch involving thrombospondin-1. Proceedings of the National Academy of Sciences of the United States of America 2005 102 37 13147 13152 2-s2.0-24944556468 10.1073/pnas.0502979102 (Pubitemid 41324993)
92. Valko M., Morris H., Mazúr M., Rapta P., Bilton R. F., Oxygen free radical generating mechanisms in the colon: do the semiquinones of vitamin K play a role in the aetiology of colon cancer? Biochimica et Biophysica Acta 2001 1527 3 161 166 2-s2.0-0035882503 10.1016/S0304-4165(01)00163-5 (Pubitemid 32710142)
93. Ďuračková Z., Ďuračková Z., Knasmüller S., Oxidants, antioxidants and redox stress. The Activity of Natural Compounds in Diseases Prevention and Therapy 2007 Bratislava, Slovakia SAP 11 59
94. Dvorakova M., Höhler B., Vollerthun R., Fischbach T., Kummer W., Macrophages: a major source of cytochrome b558 in the rat carotid body. Brain Research 2000 852 2 349 354 2-s2.0-0343819956 10.1016/S0006-8993(99)02156-3 (Pubitemid 30035172)
95. 2+ influx in human neutrophil granulocytes. Alterations in chronic granulomatous disease. Journal of Biological Chemistry 1997 272 42 26471 26478 2-s2.0-0030611889 10.1074/jbc.272.42.26471 (Pubitemid 27458866)
96. Cheng G., Cao Z., Xu X., Meir E. G. V., Lambeth J. D., Homologs of gp91phox: cloning and tissue expression of Nox3, Nox4, and Nox5. Gene 2001 269 1-2 131 140 2-s2.0-0035897653 10.1016/S0378-1119(01)00449-8 (Pubitemid 32488913)
97. Dorsam G., Taher M. M., Valerie K. C., Kuemmerle N. B., Chan J. C., Franson R. C., Diphenyleneiodium chloride blocks inflammatory cytokine-induced up-regulation of group IIA phospholipase A(2) in rat mesangial cells. Journal of Pharmacology and Experimental Therapeutics 2000 292 1 271 279 (Pubitemid 30026381)
98. Racek J., Treska V., Krizan V., Holecek V., Jerabek Z., The significance of free radicals in operations of acute ischaemia of the limbs. Zeitschrift für klinische Chemie und klinische Biochemie 1995 3 103 105
99. Pechan I., Danova K., Olejarova I., Halcak L., Rendekova V., Fabian J., Oxidative stress and antioxidant defense systems in patients after heart transplantation. Wiener Klinische Wochenschrift 2003 115 17-18 648 651 2-s2.0-0142228858 (Pubitemid 37328535)
100. Ballinger S. W., Mitochondrial dysfunction in cardiovascular disease. Free Radical Biology and Medicine 2005 38 10 1278 1295 2-s2.0-18044383110 10.1016/j.freeradbiomed.2005.02.014 (Pubitemid 40602831)
101. Rahman A., Fazal F., Greensill J., Ainley K., Parish J. H., Hadi S. M., Strand scission in DNA induced by dietary flavonoids: role of Cu(I) and oxygen free radicals and biological consequences of scission. Molecular and Cellular Biochemistry 1992 111 1-2 3 9 2-s2.0-0026687452
102. Cherubini A., Ruggiero C., Polidori M. C., Mecocci P., Potential markers of oxidative stress in stroke. Free Radical Biology and Medicine 2005 39 7 841 852 2-s2.0-29144435788 10.1016/j.freeradbiomed.2005.06.025
103. Singh K. P., Ahmad A. H., Hore S. K., Singh V., Lohani M., Rahal A., Effect of Emblica officinalis on antioxidative and haematological parameters following mercury induced toxicity. Proceedings of the 6th Annual conference of ISVPT November 2006 Patna, India
104. Singh V., Rahal A., Singh K. P., Ahmad A. H., Effect of ethanolic extract of Withania somnifera roots on antioxidant defence in mercury induced toxicity in HepG2 cell line. Online Journal of Pharmacology and Pharmacokinetics 2009 5 65 72
105. Singh V., Rahal A., Singh K. P., Ahmad A. H., Evaluation of prophylactic potential of Withania somnifera roots extract on mercury-induced oxidative damage in various rat tissues. Journal of Veterinary Pharmacology and Toxicology 2010 9 1-2 64 67
106. Singh K. P., Ahmad A. H., Singh V., Pant K., Rahal A., Effect of Emblica officinalis fruit in combating mercury-induced hepatic oxidative stress in rats. Indian Journal of Animal Sciences 2011 81 3 260 262 2-s2.0-79952654323
107. Hampton M. B., Kettle A. J., Winterbourn C. C., Inside the neutrophil phagosome: oxidants, myeloperoxidase, and bacterial killing. Blood 1998 92 9 3007 3017 2-s2.0-0032213375 (Pubitemid 28492304)
108. Babior B. M., NADPH oxidase: an update. Blood 1999 93 5 1464 1476 2-s2.0-0033105874 (Pubitemid 29102471)
109. Rice-Evans C. A., Gopinathan V., Oxygen toxicity, free radicals and antioxidants in human disease: biochemical implications in atherosclerosis and the problems of premature neonates. Essays in Biochemistry 1995 29 39 63 2-s2.0-0029420569
110. Valero N., Mosquera J., Añez G., Levy A., Marcucci R., Melchor D. M., Differential oxidative stress Induced by dengue virus in monocytes from human neonates, adult and elderly individuals. PLoS ONE 2013 8 9 e73221 10.1371/journal.pone.0073221
111. Csillag A., Boldogh I., Pazmandi K., Magyarics Z., Gogolak P., Sur S., Rajnavolgyi E., Bacsi A., Pollen-induced oxidative stress influences both innate and adaptive immune responses via altering dendritic cell functions. Journal of Immunology 2010 184 5 2377 2385 2-s2.0-77951936033 10.4049/jimmunol.0803938
112. Stehbens W. E., Oxidative stress in viral hepatitis and AIDS. Experimental and Molecular Pathology 2004 77 2 121 132 2-s2.0-4444325607 10.1016/j.yexmp.2004.04.007 (Pubitemid 39209294)
113. Hodgson P. D., Aich P., Stookey J., Popowych Y., Potter A., Babiuk L., Griebel P. J., Stress significantly increases mortality following a secondary bacterial respiratory infection. Veterinary Research 2012 43 21 10.1186/1297-9716-43-21
114. Gordon E. E., Altered oligosaccharides as the initiating autoantigen in rheumatoid arthritis. Medical Hypotheses 1983 10 4 347 352 2-s2.0-0020633238 (Pubitemid 13136292)
115. Abu-Shakra M., Shoenfeld Y., Parasitic infection and autoimmunity. Autoimmunity 1991 9 4 337 344 2-s2.0-0025779191
116. Dalle-Donne I., Scaloni A., Giustarini D., Cavarra E., Tell G., Lungarella G., Colombo R., Rossi R., Milzani A., Proteins as biomarkers of oxidattiv/e/nitrosative stress in diseases: the contribution of redox proteomics. Mass Spectrometry Reviews 2005 24 1 55 99 2-s2.0-12444296480 10.1002/mas.20006 (Pubitemid 40146422)
117. Allison M. E., Fearon D. T., Enhanced immunogenicity of aldehyde bearing antigens: a possible link between innate and adaptive immunity. European Journal of Immunology 2000 10 2881 2887
118. Scofield R. H., Kurien B. T., Ganick S., McClain M. T., Pye Q., James J. A., Schneider R. I., Broyles R. H., Bachmann M., Hensley K., Modification of lupus-associated 60-kDa Ro protein with the lipid oxidation product 4-hydroxy-2-nonenal increases antigenicity and facilitates epitope spreading. Free Radical Biology and Medicine 2005 38 6 719 728 2-s2.0-13844296394 10.1016/j.freeradbiomed.2004.11.001 (Pubitemid 40249742)
119. Trigwell S. M., Radford P. M., Page S. R., Loweth A. C., James R. F. L., Morgan N. G., Todd I., Islet glutamic acid decarboxylase modified by reactive oxygen species is recognized by antibodies from patients with type 1 diabetes mellitus. Clinical and Experimental Immunology 2001 126 2 242 249 2-s2.0-0034773277 10.1046/j.1365-2249.2001.01653.x (Pubitemid 32995138)
120. Casciola-Rosen L., Wigley F., Rosen A., Scleroderma autoantigens are uniquely fragmented by metal-catalyzed oxidation reactions: implications for pathogenesis. Journal of Experimental Medicine 1997 185 1 71 79 2-s2.0-0031025143 10.1084/jem.185.1.71 (Pubitemid 27039442)
121. Buttari B., Profumo E., Mattei V., Siracusano A., Ortona E., Margutti P., Salvati B., Sorice M., Riganò R., Oxidized β 2-glycoprotein I induces human dendritic cell maturation and promotes a T helper type 1 response. Blood 2005 106 12 3880 3887 2-s2.0-28444445251 10.1182/blood-2005-03-1201 (Pubitemid 41739027)
122. Gandy S. E., Buse M. G., Crouch R. K., Protective role of superoxide dismutase against diabetogenic drugs. Journal of Clinical Investigation 1982 70 3 650 658 2-s2.0-0019951421 (Pubitemid 12054591)
123. Gerling I. C., Oxidative Stress, altered-Self and autoimmunity. The Open Autoimmunity Journal 2009 1 33 36 10.2174/1876894600901010033
124. Stojanovich L., Stress and autoimmunity. Autoimmunity Reviews 2010 9 5 A271 A276 2-s2.0-77649273477 10.1016/j.autrev.2009.11.014
125. Nathan C., Shiloh M. U., Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens. Proceedings of the National Academy of Sciences of the United States of America 2000 97 16 8841 8848 2-s2.0-0034255209 10.1073/pnas.97.16.8841 (Pubitemid 30626635)
126. Sorci G., Faivre B., Inflammation and oxidative stress in vertebrate host-parasite systems. Philosophical Transactions of the Royal Society B 2009 364 1513 71 83 2-s2.0-58249093636 10.1098/rstb.2008.0151
127. Puertollano M. A., Puertollano E., de Cienfuegos G. Á., de Pablo M. A., Dietary antioxidants: immunity and host defense. Current Topics in Medicinal Chemistry 2011 11 14 1752 1766 2-s2.0-79959929009 10.2174/ 156802611796235107
128. Leonard S. S., Harris G. K., Shi X., Metal-induced oxidative stress and signal transduction. Free Radical Biology and Medicine 2004 37 12 1921 1942 2-s2.0-8544224992 10.1016/j.freeradbiomed.2004.09.010 (Pubitemid 39491314)
129. Kryston T. B., Georgiev A. B., Pissis P., Georgakilas A. G., Role of oxidative stress and DNA damage in human carcinogenesis. Mutation Research 2011 711 1-2 193 201 2-s2.0-79956191022 10.1016/j.mrfmmm.2010.12.016
130. Khatami M., Unresolved inflammation: "Immune tsunami" or erosion of integrity in immune-privileged and immune-responsive tissues and acute and chronic inflammatory diseases or cancer. Expert Opinion on Biological Therapy 2011 11 11 1419 1432 2-s2.0-80053643341 10.1517/14712598.2011.592826
131. O'Brien K., Fitzgerald D. C., Naiken K., Alugupalli K. R., Rostami A. M., Gran B., Role of the innate immune system in autoimmune inflammatory demyelination. Current Medicinal Chemistry 2008 15 11 1105 1115 2-s2.0-48949117588 10.2174/092986708784221458 (Pubitemid 352002979)
132. Schneider R., Mohebiany A. N., Ifergan I., Beauseigle D., Duquette P., Prat A., Arbour N., B cell-derived IL-15 enhances CD8 T cell cytotoxicity and is increased in multiple sclerosis patients. Journal of Immunology 2011 187 8 4119 4128 2-s2.0-80054774245 10.4049/jimmunol.1100885
133. Muller A. J., Sharma M. D., Chandler P. R., DuHadaway J. B., Everhart M. E., Johnson B. A. III, Kahler D. J., Pihkala J., Soler A. P., Munn D. H., Prendergast G. C., Mellor A. L., Chronic inflammation that facilitates tumor progression creates local immune suppression by inducing indoleamine 2,3 dioxygenase. Proceedings of the National Academy of Sciences of the United States of America 2008 105 44 17073 17078 2-s2.0-55949117914 10.1073/pnas.0806173105
134. Zhang K., Integration of ER stress, oxidative stress and the inflammatory response in health and disease. International Journal of Clinical and Experimental Medicine 2010 3 1 33 40 2-s2.0-77649196117
135. Davalos A. R., Coppe J., Campisi J., Desprez P., Senescent cells as a source of inflammatory factors for tumor progression. Cancer and Metastasis Reviews 2010 29 2 273 283 2-s2.0-77954563804 10.1007/s10555-010-9220-9
136. Innocenti F., Cox N. J., Dolan M. E., The use of genomic information to optimize cancer chemotherapy. Seminars in Oncology 2011 38 2 186 195 2-s2.0-79952915167 10.1053/j.seminoncol.2011.01.005
137. Vire B., David A., Wiestner A., TOSO, the Fc receptor, is highly expressed on chronic lymphocytic leukemia B cells, internalizes upon IgM binding, shuttles to the lysosome, and is downregulated in response to TLR activation. Journal of Immunology 2011 187 8 4040 4050 2-s2.0-80054751083 10.4049/jimmunol.1100532
138. Pellegriti G., Frasca F., Regalbuto C., Squatrito S., Vigneri R., Worldwide increasing incidence of thyroid cancer: update on epidemiology and
139. Romano A. D., Serviddio G., De Matthaeis A., Bellanti F., Vendemiale G., Oxidative stress and aging. Journal of Nephrology 2010 23 supplement 15 S29 S36 2-s2.0-78049451957
140. Harman D., Aging: overview. Annals of the New York Academy of Sciences 2001 928 1 21 2-s2.0-0035033142 (Pubitemid 32386063)
141. Bejma J., Ji L. L., Aging and acute exercise enhance free radical generation in rat skeletal muscle. Journal of Applied Physiology 1999 87 1 465 470 2-s2.0-0032788956 (Pubitemid 29330715)
142. Bejma B., Ramires R., Ji J., Free radical generation and oxidative stress with ageing and exercise: differential effects in the myocardium and liver. Acta Physiologica Scandinavica 2000 169 4 343 351 2-s2.0-0033817812 10.1046/j.1365-201X.2000.00745.x
143. Driver A. S., Kodavanti P. R. S., Mundy W. R., Age-related changes in reactive oxygen species production in rat brain homogenates. Neurotoxicology and Teratology 2000 22 2 175 181 2-s2.0-0034603580 10.1016/S0892-0362(99)00069-0 (Pubitemid 30176073)
144. Gomi F., Utsumi H., Hamada A., Matsuo M., Aging retards spin clearance from mouse brain and food restriction prevents its age-dependent retardation. Life Sciences 1993 52 25 2027 2033 2-s2.0-0027161461 10.1016/0024-3205(93)90687- X
145. Zhang H. J., Xu L., Drake V. J., Xie L., Oberley L. W., Kregel K. C., Heat-induced liver injury in old rats is associated with exaggerated oxidative stress and altered transcription factor activation. FASEB Journal 2003 17 15 2293 2295 2-s2.0-0642364454 10.1096/fj.03-0139fje (Pubitemid 39561470)
146. Kregel K. C., Zhang H. J., An integrated view of oxidative stress in aging: basic mechanisms, functional effects, and pathological considerations. American Journal of Physiology 2007 292 1 R18 R36 2-s2.0-33846243745 10.1152/ajpregu.00327.2006 (Pubitemid 46091599)
147. Hagen T. M., Oxidative stress, redox imbalance, and the aging process. Antioxidants and Redox Signaling 2003 5 5 503 506 2-s2.0-0142213548 (Pubitemid 37315137)
148. Babbar N., Gerner E. W., Targeting polyamines and inflammation for cancer prevention. Recent Results in Cancer Research 2011 188 49 64 2-s2.0-79551533724 10.1007/978-3-642-10858-7-4
149. Shames D. S., Minna J. D., Gazdar A. F., DNA methylation in health, disease, and cancer. Current Molecular Medicine 2007 7 1 85 102 2-s2.0-33847317873 10.2174/156652407779940413 (Pubitemid 46322281)
150. Aubert G., Lansdorp P. M., Telomeres and aging. Physiological Reviews 2008 88 2 557 579 2-s2.0-42149185640 10.1152/physrev.00026.2007 (Pubitemid 351522746)
151. Zingg J. M., Azzi A., Meydani M., Genetic polymorphisms as determinants for disease-preventive effects of vitamin E. Nutrition Reviews 2008 66 7 406 414 2-s2.0-47349106545 10.1111/j.1753-4887.2008.00050.x (Pubitemid 352000151)
152. Khatami M., Inflammation, aging, and cancer: tumoricidal versus tumorigenesis of immunity. Cell Biochemistry and Biophysics 2009 55 2 55 79 2-s2.0-71449114145 10.1007/s12013-009-9059-2
153. Laddha N. C., Dwivedi M., Mansuri M. S., Gani A. R., Ansarullah M., Ramachandran A. V., Dalai S., Begum R., Vitiligo: interplay between oxidative stress and immune system. Experimental Dermatology 2013 22 4 245 250 10.1111/exd.12103
154. Erbay E., Babaev V. R., Mayers J. R., Makowski L., Charles K. N., Snitow M. E., Fazio S., Wiest M. M., Watkins S. M., Linton M. F., Hotamisligil G. S., Reducing endoplasmic reticulum stress through a macrophage lipid chaperone alleviates atherosclerosis. Natural Medicine 2009 15 1383 1391 10.1038/nm.2067
155. Albano E., Oxidative mechanisms in the pathogenesis of alcoholic liver disease. Molecular Aspects of Medicine 2008 29 1-2 9 16 2-s2.0-39749090649 10.1016/j.mam.2007.09.004 (Pubitemid 351312214)
156. Halliwell B., Oxidative stress and neurodegeneration: where are we now? Journal of Neurochemistry 2006 97 6 1634 1658 2-s2.0-33745013111 10.1111/j.1471-4159.2006.03907.x (Pubitemid 43873658)
157. Brown L. A., Harris F. L., Jones D. P., Ascorbate deficiency and oxidative stress in the alveolar type II cell. American Journal of Physiology 1997 273 4 L782 L788 2-s2.0-0030725481
158. Markesbery W. R., Oxidative stress hypothesis in Alzheimer's disease. Free Radical Biology and Medicine 1997 23 1 134 147 2-s2.0-0030915855 10.1016/S0891-5849(96)00629-6 (Pubitemid 27217017)
159. Butterfield D. A., Kanski J., Brain protein oxidation in age-related neurodegenerative disorders that are associated with aggregated proteins. Mechanisms of Ageing and Development 2001 122 9 945 962 2-s2.0-0035880007 10.1016/S0047-6374(01)00249-4 (Pubitemid 32441616)
160. Butterfield D. A., Lauderback C. M., Lipid peroxidation and protein oxidation in Alzheimer's disease brain: potential causes and consequences involving amyloid β -peptide-associated free radical oxidative stress. Free Radical Biology and Medicine 2002 32 11 1050 1060 2-s2.0-0036591849 10.1016/S0891-5849(02)00794-3 (Pubitemid 34603342)
161. Giasson B. I., Ischiropoulos H., Lee V. M.-Y., Trojanowski J. Q., The relationship between oxidative/nitrative stress and pathological inclusions in Alzheimer's and Parkinson's diseases. Free Radical Biology and Medicine 2002 32 12 1264 1275 2-s2.0-0037096193 10.1016/S0891-5849(02)00804-3 (Pubitemid 34607630)
162. Zhu X., Smith M. A., Perry G., Aliev G., Mitochondrial failures in Alzheimer's disease. American Journal of Alzheimer's Disease and other Dementias 2004 19 6 345 352 2-s2.0-10044283223 (Pubitemid 39612927)
163. Dalle-Donne I., Rossi R., Colombo R., Giustarini D., Milzani A., Biomarkers of oxidative damage in human disease. Clinical Chemistry 2006 52 4 601 623 2-s2.0-33645459044 10.1373/clinchem.2005.061408
164. Kurien B. T., Hensley K., Bachmann M., Scofield R. H., Oxidatively modified autoantigens in autoimmune diseases. Free Radical Biology and Medicine 2006 41 4 549 556 2-s2.0-33746033343 10.1016/j.freeradbiomed.2006.05.020 (Pubitemid 44080517)
165. Halliwell B., Are polyphenols antioxidants or pro-oxidants? What do we learn from cell culture and in vivo studies? Archives of Biochemistry and Biophysics 2008 476 2 107 112 2-s2.0-48349140474 10.1016/j.abb.2008.01.028
166. Sahu S. C., Gray G. C., Interactions of flavonoids, trace metals, and oxygen: nuclear DNA damage and lipid peroxidation induced by myricetin. Cancer Letters 1993 70 1-2 73 79 2-s2.0-0027328277 (Pubitemid 23219862)
167. Sahu S. C., Gray G. C., Kaempferol-induced nuclear DNA damage and lipid peroxidation. Cancer Letters 1994 85 2 159 164 2-s2.0-0028068478 10.1016/0304-3835(94)90269-0 (Pubitemid 24302954)
168. Ahmad M. S., Fazal F., Rahman A., Hadi S. M., Parish J. H., Activities of flavonoids for the cleavage of DNA in the presence of Cu(II): correlation with generation of active oxygen species. Carcinogenesis 1992 13 4 605 608 2-s2.0-0026594634
169. Rice-Evans C. A., Miller N. J., Bolwell P. G., Bramley P. M., Pridham J. B., The relative antioxidant activities of plant-derived polyphenolic flavonoids. Free Radical Research 1995 22 4 375 383 2-s2.0-0028999867
170. Guohua G., Emin S., Ronald L., Antioxidant and prooxidant behavior of flavonoids: structure-activity relationships. Free Radical Biology and Medicine 1997 22 5 749 760 2-s2.0-0031020195 10.1016/S0891-5849(96)00351-6 (Pubitemid 27058337)
171. Ioku K., Tsushida T., Takei Y., Nakatani N., Terao J., Antioxidative activity of quercetin and quercetin monoglucosides in solution and phospholipid bilayers. Biochimica et Biophysica Acta 1995 1234 1 99 104 2-s2.0-0028904605 10.1016/0005-2736(94)00262-N
172. Igile G. O., Oleszek W., Jurzysta M., Burda S., Fafunso M., Fasanmade A. A., Flavonoids from Vernonia amygdalina and their antioxidant activities. Journal of Agricultural and Food Chemistry 1994 42 11 2445 2448 2-s2.0-0000099151
173. Weiss G., Werner-Felmayer G., Werner E. R., Grünewald K., Wachter H., Hentze M. W., Iron regulates nitric oxide synthase activity by controlling nuclear transcription. Journal of Experimental Medicine 1994 180 3 969 976 2-s2.0-0028059950 10.1084/jem.180.3.969 (Pubitemid 24256609)
174. Laughton M. J., Evans P. J., Moroney M. A., Hoult J. R. S., Halliwell B., Inhibition of mammalian 5-lipoxygenase and cyclo-oxygenase by flavonoids and phenolic dietary additives. Relationship to antioxidant activity and to iron ion-reducing ability. Biochemical Pharmacology 1991 42 9 1673 1681 2-s2.0-0026095778 10.1016/0006-2952(91)90501-U
175. Lin A. P., Tsai W. J., Fan C. Y., Lee M. J., Vandellia cordifolia regulated cell proliferation and cytokines production in human mononuclear cells. American Journal of Chinese Medicine 2000 28 3-4 313 323 2-s2.0-0034566996
176. Lee J., Hahm E. R., Singh S. V., Withaferin A inhibits activation of signal transducer and activator of transcription 3 in human breast cancer cells. Carcinogenesis 2010 31 11 1991 1998 2-s2.0-78149239365 10.1093/carcin/bgq175
177. Lastra C. A., Villegas I., Resveratrol as an antioxidant and pro-oxidant agent: mechanisms and clinical implications. Biochemical Society Transactions 2007 35 5 1156 1160 2-s2.0-36749081135 10.1042/BST0351156 (Pubitemid 350206449)
178. Seo M. Y., Lee S. M., Protective effect of low dose of ascorbic acid on hepatobiliary function in hepatic ischemia/reperfusion in rats. Journal of Hepatology 2002 36 1 72 77 2-s2.0-0036128306 10.1016/S0168-8278(01)00236-7 (Pubitemid 34234019)
179. Buettner G. R., Jurkiewicz B. A., Catalytic metals, ascorbate and free radicals: combinations to avoid. Radiation Research 1996 145 5 532 541 2-s2.0-0029939394 10.2307/3579271 (Pubitemid 26127160)
180. Buettner G. R., The pecking order of free radicals and antioxidants: lipid peroxidation, α -tocopherol, and ascorbate. Archives of Biochemistry and Biophysics 1993 300 2 535 543 2-s2.0-0027251053 10.1006/abbi.1993.1074 (Pubitemid 23232908)
181. Zhang F.-F., Zheng Y.-F., Zhu H.-J., Shen X.-Y., Zhu X.-Q., Effects of kaempferol and quercetin on cytochrome 450 activities in primarily cultured rat hepatocytes. Zhejiang Da Xue Xue Bao Yi Xue Ban 2006 35 1 18 22 2-s2.0-39049189110
182. Yao H.-T., Luo M.-N., Hung L.-B., Chiang M.-T., Lin J.-H., Lii C., Huang C., Effects of chitosan oligosaccharides on drug-metabolizing enzymes in rat liver and kidneys. Food and Chemical Toxicology 2012 50 5 1171 1177 2-s2.0-84857940260 10.1016/j.fct.2012.02.022
183. Hebbar V., Shen G., Hu R., Kim B., Chen C., Korytko P. J., Crowell J. A., Levine B. S., Kong A.-N. T., Toxicogenomics of resveratrol in rat liver. Life Sciences 2005 76 20 2299 2314 2-s2.0-14644410484 10.1016/j.lfs.2004.10.039 (Pubitemid 40313418)
184. Young A. J., Lowe G. M., Antioxidant and prooxidant properties of carotenoids. Archives of Biochemistry and Biophysics 2001 385 1 20 27 2-s2.0-0034775553 10.1006/abbi.2000.2149 (Pubitemid 32988978)
185. Kontush A., Finckh B., Karten B., Kohlschütter A., Beisiegel U., Antioxidant and prooxidant activity of α -tocopherol in human plasma and low density lipoprotein. Journal of Lipid Research 1996 37 7 1436 1448 2-s2.0-0029890611 (Pubitemid 26249975)
186. Scott B. C., Aruoma O. I., Evansi P. J., O'Neill C., Van Der Vliet A., Cross C. E., Tritschler H. A., Halliwell B., Lipoic and dihydrolipoic acids as antioxidants. A critical evaluation. Free Radical Research 1994 20 2 119 133 2-s2.0-0028345285 (Pubitemid 24103740)
187. Moini H., Packer L., Saris N. L., Antioxidant and prooxidant activities of α -lipoic acid and dihydrolipoic acid. Toxicology and Applied Pharmacology 2002 182 1 84 90 2-s2.0-0036070514 10.1006/taap.2002.9437 (Pubitemid 34775480)
188. Rasool M., Varalakshmi P., Immunomodulatory role of Withania somnifera root powder on experimental induced inflammation: an in vivo and in vitro study. Vascular Pharmacology 2006 44 6 406 410 2-s2.0-33646787097 10.1016/j.vph.2006. 01.015 (Pubitemid 43766670)
189. Ahmad M., Saleem S., Ahmad A. S., Ansari M. A., Yousuf S., Hoda M. N., Islam F., Neuroprotective effects of Withania somnifera on 6-hydroxydopamine induced Parkinsonism in rats. Human and Experimental Toxicology 2005 24 3 137 147 2-s2.0-18044398197 10.1191/0960327105ht509oa (Pubitemid 40605154)
190. Owais M., Sharad K. S., Shehbaz A., Saleemuddin M., Antibacterial efficacy of Withania somnifera (ashwagandha) an indigenous medicinal plant against experimental murine salmonellosis. Phytomedicine 2005 12 3 229 235 2-s2.0-14844321614 10.1016/j.phymed.2003.07.012 (Pubitemid 40348625)
191. Gupta S. K., Mohanty I., Talwar K. K., Dinda A., Joshi S., Bansal P., Saxena A., Arya D. S., Cardioprotection from ischemia and reperfusion injury by Withania somnifera: a hemodynamic, biochemical and histopathological assessment. Molecular and Cellular Biochemistry 2004 260 1 39 47 2-s2.0-4344577070 10.1023/B:MCBI.0000026051.16803.03 (Pubitemid 39127570)
192. Srinivasan S., Ranga R. S., Burikhanov R., Han S., Chendil D., Par-4-dependent apoptosis by the dietary compound withaferin A in prostate cancer cells. Cancer Research 2007 67 1 246 253 2-s2.0-33846436451 10.1158/0008-5472.CAN-06-2430 (Pubitemid 46142781)
193. Malik F., Kumar A., Bhushan S., Khan S., Bhatia A., Suri K. A., Qazi G. N., Singh J., Reactive oxygen species generation and mitochondrial dysfunction in the apoptotic cell death of human myeloid leukemia HL-60 cells by a dietary compound withaferin A with concomitant protection by N-acetyl cysteine. Apoptosis 2007 12 11 2115 2133 2-s2.0-34848858255 10.1007/s10495-007-0129-x (Pubitemid 47498235)
194. Stan S. D., Hahm E., Warin R., Singh S. V., Withaferin A causes FOXO3a- and Bim-dependent apoptosis and inhibits growth of human breast cancer cells in vivo. Cancer Research 2008 68 18 7661 7669 2-s2.0-54749130365 10.1158/0008-5472.CAN-08-1510
195. Stan S. D., Zeng Y., Singh S. V., Ayurvedic medicine constituent withaferin a causes G2 and M phase cell cycle arrest in human breast cancer cells. Nutrition and Cancer 2008 60 1 51 60 2-s2.0-55949092309 10.1080/01635580802381477
196. Oh J. H., Lee T., Kim S. H., Choi Y. H., Lee S. H., Lee J. M., Kim Y., Park J., Kwon T. K., Induction of apoptosis by withaferin A in human leukemia U937 cells through down-regulation of Akt phosphorylation. Apoptosis 2008 13 12 1494 1504 2-s2.0-56349123756 10.1007/s10495-008-0273-y
197. Mandal C., Dutta A., Mallick A., Chandra S., Misra L., Sangwan R. S., Mandal C., Withaferin A induces apoptosis by activating p38 mitogen-activated protein kinase signaling cascade in leukemic cells of lymphoid and myeloid origin through mitochondrial death cascade. Apoptosis 2008 13 12 1450 1464 2-s2.0-56349141560 10.1007/s10495-008-0271-0
198. Yu Y., Hamza A., Zhang T., Gu M., Zou P., Newman B., Li Y., Gunatilaka A. A. L., Zhan C., Sun D., Withaferin A targets heat shock protein 90 in pancreatic cancer cells. Biochemical Pharmacology 2010 79 4 542 551 2-s2.0-71549153791 10.1016/j.bcp.2009.09.017
199. Hahm E. R., Moura M. B., Kelley E. E., van Houten B., Shiva S., Singh S. V., Withaferin a-induced apoptosis in human breast cancer cells is mediated by reactive oxygen species. PLoS ONE 2011 6 8 2-s2.0-80051512168 10.1371/journal.pone.0023354 e23354
200. Schulz V., Hänsel R., Tyler V., Rational Phytotherapy: A Physician's Guide to Herbal Medicine 1998 Berlin, Germany Springer
201. Attele A. S., Wu J. A., Yuan C., Ginseng pharmacology: multiple constituents and multiple actions. Biochemical Pharmacology 1999 58 11 1685 1693 2-s2.0-0344549853 10.1016/S0006-2952(99)00212-9 (Pubitemid 29505408)
202. Huang K. C., Pharmacology of Chinese Herbs 1999 Boca Raton, Fla, USA CRC Press
203. Blumenthal M., Goldberg A., Brinckmann J., Herbal medicine: expanded commission E monographs. Integrative Medicine Communications 2000 133 6 487 10.7326/0003-4819-133-6-200009190-00031
204. Bruneton J., Pharmacognosy, Phytochemistry, Medicinal Plants 1995 Paris, France Lavisior
205. Dewick P. M., Medicinal Natural Products 1997 West Sussex, UK John Wiley & Sons
206. Beatty S., Koh H., Phil M., Henson D., Boulton M., The role of oxidative stress in the pathogenesis of age-related macular degeneration. Survey of Ophthalmology 2000 45 2 115 134 2-s2.0-0033795036 10.1016/S0039-6257(00)00140-5
207. Maritim A. C., Sanders R. A., Watkins J. B. III, Diabetes, oxidative stress, and antioxidants: a review. Journal of Biochemical and Molecular Toxicology 2003 17 1 24 38 2-s2.0-0037253073 10.1002/jbt.10058 (Pubitemid 36410972)
208. Fulle S., Pietrangelo T., Mancinelli R., Saggini R., Fanò G., Specific correlations between muscle oxidative stress and chronic fatigue syndrome: a working hypothesis. Journal of Muscle Research and Cell Motility 2007 28 6 355 362 2-s2.0-41049087200 10.1007/s10974-008-9128-y
209. Singh U., Jialal I., Oxidative stress and atherosclerosis. Pathophysiology 2006 13 3 129 142 2-s2.0-33745713661 10.1016/j.pathophys.2006. 05.002
210. Uttara B., Singh A. V., Zamboni P., Mahajan R. T., Oxidative stress and neurodegenerative diseases: a review of upstream and downstream antioxidant therapeutic options. Current Neuropharmacology 2009 7 1 65 74 2-s2.0-65949121134 10.2174/157015909787602823
211. Cho Y. S., Moon H., The role of oxidative stress in the pathogenesis of asthma. Allergy, Asthma and Immunology Research 2010 2 3 183 187 2-s2.0-77954049188 10.4168/aair.2010.2.3.183
212. Blackburn A. C., Coggan M., Shield A. J., Cappello J., Theodoratos A., Murray T. P., Rooke M., Larter C. Z., Koina M. E., Dahlstrom J. E., Matthaei K. I., Board P. G., Glutathione transferase kappa deficiency causes glomerular nephropathy without overt oxidative stress. Laboratory Investigation 2011 91 11 1572 1583 2-s2.0-80155151944 10.1038/labinvest.2011.107
213. Ziskoven C., Jäger M., Zilkens C., Bloch W., Brixius K., Krauspe R., Oxidative stress in secondary osteoarthritis: from cartilage destruction to clinical presentation? Orthopedic Reviews 2010 2 2 e23
214. Sander C. S., Hamm F., Elsner P., Thiele J. J., Oxidative stress in malignant melanoma and non-melanoma skin cancer. British Journal of Dermatology 2003 148 5 913 922 2-s2.0-0037525665 10.1046/j.1365-2133.2003.05303.x (Pubitemid 36750783)
215. Filippo C. D., Cuzzocrea S., Rossi F., Marfella R., D'Amico M., Oxidative stress as the leading cause of acute myocardial infarction in diabetics. Cardiovascular Drug Reviews 2006 24 2 77 87 2-s2.0-33846522832 10.1111/j.1527-3466.2006.00077.x (Pubitemid 46696918)