Effects of different environmental oxygen levels on free radical processes in fish

Free radicals in biology and medicine

(1991) · General Pharmacology: The Vascular System · doi:10.1016/0306-3623(91)90478-o · Cited by 17,178

Critical Review of Rate Constants for Reactions of Hydrated Electrons, Hydrogen Atoms and Hydroxyl Radicals (OH/O−) in Aqueous Solution

Buxton, G. V., Greenstock, C. L., Helman, W. P., & Ross, A. B. (1988) · Journal of Physical and Chemical Reference Data · doi:10.1063/1.555805 · Cited by 12,332

Free Radicals in the Physiological Control of Cell Function

Dröge, W. (2002) · Physiological Reviews · doi:10.1152/physrev.00018.2001 · Cited by 9,855

Oxidative stress: oxidants and antioxidants

Sies, H. (1997) · Experimental Physiology · doi:10.1113/expphysiol.1997.sp004024 · Cited by 4,566

Laboratory techniques in biochemistry and molecular biology

Work, T. S., & Work, E. (1973) · Food and Cosmetics Toxicology · doi:10.1016/0015-6264(73)90270-8 · Cited by 2,179

Molecular biomarkers of oxidative stress in aquatic organisms in relation to toxic environmental pollutants

Valavanidis, A., Vlahogianni, T., Dassenakis, M., & Scoullos, M. (2006) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2005.03.013 · Cited by 1,795

OXIDATION OF FREE AMINO ACIDS AND AMINO ACID RESIDUES IN PROTEINS BY RADIOLYSIS AND BY METAL-CATALYZED REACTIONS

Stadtman, E. R. (1993) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.62.070193.004053 · Cited by 1,395

Prooxidant and antioxidant mechanisms in aquatic organisms

Winston, G. W., & Di Giulio, R. T. (1991) · Aquatic Toxicology · doi:10.1016/0166-445x(91)90033-6 · Cited by 1,353

Lipid peroxidation—DNA damage by malondialdehyde

Marnett, L. J. (1999) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/s0027-5107(99)00010-x · Cited by 1,304

Oxidative stress and gene regulation

Allen, R. G., & Tresini, M. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00242-7 · Cited by 1,302

Importance of SE-glutathione peroxidase, catalase, and CU/ZN-SOD for cell survival against oxidative stress

Michiels, C., Raes, M., Toussaint, O., & Remacle, J. (1994) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(94)90079-5 · Cited by 1,193

Oxidative Stress: Oxidants and Antioxidants.

Haddock, P. (1992) · Cardiovascular Research · doi:10.1093/cvr/26.8.816a · Cited by 1,185

Analysis of a form of oxidative DNA damage, 8-hydroxy-2′-deoxyguanosine, as a marker of cellular oxidative stress during carcinogenesis

Kasai, H. (1997) · Mutation Research/Reviews in Mutation Research · doi:10.1016/s1383-5742(97)00035-5 · Cited by 1,139

Protein Oxidation

STADTMAN, E. R., & LEVINE, R. L. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06187.x · Cited by 1,007

Free Radicals in Biology and Medicine

Kovacic, P. (1986) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.2600750133 · Cited by 982

Biochemical Adaptation

Hochachka, P. W., & Somero, G. N. (1984) · Princeton University Press eBooks · doi:10.1515/9781400855414 · Cited by 913

Oxidative stress: animal adaptations in nature.

Storey, K. B. (1996) · PubMed · Cited by 712

The mammalian basic helix–loop–helix/PAS family of transcriptional regulators

Kewley, R. J., Whitelaw, M. L., & Chapman-Smith, A. (2004) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(03)00211-5 · Cited by 589

Animal response to drastic changes in oxygen availability and physiological oxidative stress

Hermes-Lima, M., & Zenteno-Savı́n, T. (2002) · Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology · doi:10.1016/s1532-0456(02)00080-7 · Cited by 587

Biochemical responses in aquatic animals: A review of determinants of oxidative stress

Di Giulio, R. T., Washburn, P. C., Wenning, R. J., Winston, G. W., & Jewell, C. S. (1989) · Environmental Toxicology and Chemistry · doi:10.1002/etc.5620081203 · Cited by 550

BIOCHEMICAL RESPONSES IN AQUATIC ANIMALS: A REVIEW OF DETERMINANTS OF OXIDATIVE STRESS

Di Giulio, R. T., Washburn, P. C., Wenning, R. J., Winston, G. W., & Jewell, C. S. (1989) · Environmental Toxicology and Chemistry · doi:10.1897/1552-8618(1989)8[1103:briaaa]2.0.co;2 · Cited by 490

Mammalian Oxygen Sensing, Signalling and Gene Regulation

Wenger, R. H. (2000) · Journal of Experimental Biology · doi:10.1242/jeb.203.8.1253 · Cited by 453

Oxidative stress in toxicology: established mammalian and emerging piscine model systems.

Kelly, K. A., Havrilla, C. M., Brady, T. C., Abramo, K. H., & Levin, E. D. (1998) · Environmental Health Perspectives · doi:10.1289/ehp.98106375 · Cited by 450

Functions of glutathione and glutathione disulfide in immunology and immunopathology

Dröge, W., Schulze‐Osthoff, K., Mihm, S., Galter, D., Schenk, H., Eck, H., Roth, S., & Gmünder, H. (1994) · The FASEB Journal · doi:10.1096/fasebj.8.14.7958618 · Cited by 444

Oxygen in Biology and Biochemistry: Role of Free Radicals

Hermes‐Lima, M. (2004) · Functional Metabolism · doi:10.1002/047167558x.ch12 · Cited by 438

Techniques in Free Radical Research

(1991) · Laboratory Techniques in Biochemistry and Molecular Biology · doi:10.1016/s0075-7535(08)x7003-2 · Cited by 430

Oxidative stress and antioxidant defenses in goldfish Carassius auratus during anoxia and reoxygenation

Lushchak, V. I., Lushchak, L. P., Mota, A. A., & Hermes-Lima, M. (2001) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.280.1.r100 · Cited by 392

Antioxidant defenses and metabolic depression. The hypothesis of preparation for oxidative stress in land snails

Hermes-Lima, M., Storey, J. M., & Storey, K. B. (1998) · Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology · doi:10.1016/s0305-0491(98)10053-6 · Cited by 347

Hypoxia and recovery perturb free radical processes and antioxidant potential in common carp (Cyprinus carpio) tissues

Lushchak, V. I., Bagnyukova, T. V., Lushchak, O. V., Storey, J. M., & Storey, K. B. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.01.006 · Cited by 320

Modification of glucose-6-phosphate dehydrogenase by 4-hydroxy-2-nonenal. Formation of cross-linked protein that inhibits the multicatalytic protease.

Friguet, B., Stadtman, E. R., & Szweda, L. I. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)31853-7 · Cited by 311

Oxygen-dependent gene expression in fishes

Nikinmaa, M., & Rees, B. B. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00626.2004 · Cited by 304

Hyperoxia results in transient oxidative stress and an adaptive response by antioxidant enzymes in goldfish tissues

Lushchak, V. I., Bagnyukova, T. V., Husak, V. V., Luzhna, L. I., Lushchak, O. V., & Storey, K. B. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.02.024 · Cited by 288

Free radicals : a practical approach

Punchard, N. A., & Kelly, F. J. (1996) · Oxford University Press eBooks · Cited by 285

Functional Metabolism: Regulation and Adaptation

Dillon, P. (2005) · American Journal of Human Biology · doi:10.1002/ajhb.20135 · Cited by 285

DNA and Free Radicals

Aruoma, O. I., Halliwell, B. B., & DPhil, B. H. (1993) · Medical Entomology and Zoology · Cited by 284

Hypoxic survival strategies in two fishes: extreme anoxia tolerance in the North European crucian carp and natural hypoxic preconditioning in a coral-reef shark

Nilsson, G. E., & Renshaw, G. M. C. (2004) · Journal of Experimental Biology · doi:10.1242/jeb.00979 · Cited by 284

Functional Metabolism: Regulation and Adaptation

(2004) · Wiley eBooks · doi:10.1002/047167558x · Cited by 282

Ethanol: Novel End Product of Vertebrate Anaerobic Metabolism

Shoubridge, E. A., & Hochachka, P. W. (1980) · Science · doi:10.1126/science.7384807 · Cited by 270

mRNA expression of antioxidant enzymes (SOD, CAT and GSH-Px) and lipid peroxidative stress in liver of Atlantic salmon (Salmo salar) exposed to hyperoxic water during smoltification

Olsvik, P. A., Kristensen, T., Waagbø, R., Rosseland, B. O., Tollefsen, K.-E., Baeverfjord, G., & Berntssen, M. H. G. (2005) · Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology · doi:10.1016/j.cbpc.2005.07.009 · Cited by 243

Pathways of cell signaling in hyperoxia

Lee, P. J., & Choi, A. M. K. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(03)00279-x · Cited by 180

Introduction

FitzGerald, G. (2001) · Trends in Cardiovascular Medicine · doi:10.1016/s1050-1738(01)00122-0 · Cited by 166

Exposure of Yeast Cells to Anoxia Induces Transient Oxidative Stress

Dirmeier, R., O’Brien, K. M., Engle, M., Dodd, A., Spears, E., & Poyton, R. Ο. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203902200 · Cited by 154

Carbonic Anhydrase III. OXIDATIVE MODIFICATION IN VIVO AND LOSS OF PHOSPHATASE ACTIVITY DURING AGING

Cabiscol, E., & Levine, R. L. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.24.14742 · Cited by 148

Modification of hepatic proteins in rats exposed to high oxygen concentration

Starke-Reed, P. E., Oliver, C. N., & Stadtman, E. R. (1987) · The FASEB Journal · doi:10.1096/fasebj.1.1.2886388 · Cited by 109

Catalase inhibition by amino triazole induces oxidative stress in goldfish brain

Bagnyukova, T., Vasylkiv, O. Y., Storey, K. B., & Lushchak, V. I. (2005) · Brain Research · doi:10.1016/j.brainres.2005.06.002 · Cited by 107

Effects of dietary ascorbic acid on oxygen stress (hypoxia or hyperoxia), growth and tissue vitamin concentrations in juvenile rainbow trout (Oncorhynchus mykiss)

Dabrowski, K. R., Lee, K., Guz, L., Verlhac-Trichet, V., & Gabaudan, J. (2003) · Aquaculture · doi:10.1016/j.aquaculture.2003.09.047 · Cited by 103

Elevated Protein Carbonyls and Lipid Peroxidation Products Correlating with Myeloperoxidase in Tracheal Aspirates from Premature Infants

Buss, I. H., Darlow, B. A., & Winterbourn, C. C. (2000) · Pediatric Research · doi:10.1203/00006450-200005000-00014 · Cited by 91

The effects of hypoxia and paraquat on the superoxide dismutase activity in different organs of carp, Cyprinus carpio L.

Víg, É., & Nemcsók, J. (1989) · Journal of Fish Biology · doi:10.1111/j.1095-8649.1989.tb03389.x · Cited by 82

Adaptive response of antioxidant enzymes to catalase inhibition by aminotriazole in goldfish liver and kidney

Bagnyukova, T., Storey, K. B., & Lushchak, V. I. (2005) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2005.08.003 · Cited by 82

Anaerobic metabolism of goldfish, Carassius auratus (L.): Ethanol and CO2 excretion rates and anoxia tolerance at 20, 10 and 5°C

van den Thillart, G., Berge-Henegouwen, M. V., & Kesbeke, F. (1983) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(83)90330-4 · Cited by 71

Iron-catalyzed oxidative modification of glucose-6-phosphate dehydrogenase from Leuconostoc mesenteroides. Structural and functional changes.

Szweda, L. I., & Stadtman, E. R. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50699-8 · Cited by 59

Oxygen-Dependent Energetics of Anoxia-Tolerant and Anoxia-Intolerant Hepatocytes

Krumschnabel, G., Schwarzbaum, P. J., Lisch, J., Biasi, C., & Wieser, W. (2000) · Journal of Experimental Biology · doi:10.1242/jeb.203.5.951 · Cited by 41

Effect of ozone exposure on the compositions of gill and erythrocyte membrane lipids and proteins of Japanese charr (Salvelinus leucomaenis)

Fukunaga, K., Suzuki, T., & Takama, K. (1991) · Comparative Biochemistry and Physiology Part B Comparative Biochemistry · doi:10.1016/0305-0491(91)90208-u · Cited by 16

Environmentally induced oxidative stress in aquatic animals

Lushchak, V. I. (2011) · Aquatic Toxicology · doi:10.1016/j.aquatox.2010.10.006 · Cited by 2,729

Animal performance and stress: responses and tolerance limits at different levels of biological organisation

Kassahn, K. S., Crozier, R. H., Pörtner, H. O., & Caley, M. J. (2009) · Biological Reviews · doi:10.1111/j.1469-185x.2008.00073.x · Cited by 263

Polystyrene nanoplastic induces ROS production and affects the MAPK-HIF-1/NFkB-mediated antioxidant system in Daphnia pulex

Liu, Z., Huang, Y., Jiao, Y., Chen, Q., Wu, D., Yu, P., Li, Y., Cai, M., & Zhao, Y. (2020) · Aquatic Toxicology · doi:10.1016/j.aquatox.2020.105420 · Cited by 253

Hypoxia Tolerance in Animals: Biology and Application

Gorr, T. A., Wichmann, D., Hu, J., Hermes‐Lima, M., Welker, A. F., Terwilliger, N., Wren, J. F., Viney, M., Morris, S., Nilsson, G. E., et al. (2010) · Physiological and Biochemical Zoology · doi:10.1086/648581 · Cited by 134