Cited by 157Redox biology and oxidative stressFree Radicals and AntioxidantsPhotosynthetic Processes and Mechanisms

The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.

The oxidation of tiron by superoxide anion. Kinetics of the reaction in aqueous solution and in chloroplasts

Greenstock, C.L., Miller, R.W.·1975·Biochimica et Biophysica Acta (BBA) - Bioenergetics

Open this paper in CoChat — free account

Abstract

The rate of reaction between superoxide anion (O2) and 1,2-dihydroxybenzene-3,5-disulfonic acid (tiron) was measured with pulse radiolysis-generated O2. A kinetic spectrophotometric method utilizing competition between p-benzoquinone and tiron for O2 was employed. In this system, the known rate of reduction of p-benzoquinone was compared with the rate of oxidation of tiron to the semiquinone. From the concentration dependence of the rate of tiron oxidation, the absolute second order rate constant for the reaction was determined to be 5x10-8 M-minus1-s-minus1. Ascorbate reduced O2 to hydrogen peroxide with a rate constant of 10-8 M-minus1-s-minus1 as determined by the same method. The tiron semiquinone may be used as an indicator free radical for the formation of superoxide anion in biological systems because of the rapid rate of oxidation of the catechol by O2 compared to the rate of O2 formation is most enzymatic systems. Tiron oxidation was used to follow the formation of superoxide anion in swollen chloroplasts. The chloroplasts photochemically reduced molecular oxygen which was further reduced to hydrogen peroxide by tiron. Tiron oxidation specifically required O2 since O2 was consumed in the reaction and tiron did not reduce the P700 cation radical or other components of Photosystem I under anaerobic conditions.

Integrity signals

Registry

Crossref · 10.1016/0005-2728(75)90184-x

Cites

12 of 12 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Acid dissociation constant and decay kinetics of the perhydroxyl radical
Béhar, D., Czapski, G., Rabani, J., Dorfman, L. M., & Schwarz, H. A. (1970) · The Journal of Physical Chemistry · doi:10.1021/j100711a009 · Cited by 499
The mechanism of the oxidation of ascorbate and Mn2+ by chloroplasts: The role of the radical superoxide
Epel, B. L., & Neumann, J. (1973) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(73)90211-9 · Cited by 133
Superoxide reduction as a mechanism of ascorbate-stimulated oxygen uptake by isolated chloroplasts
Allen, J. F., & Hall, D. O. (1973) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(73)91016-4 · Cited by 109
Pulse radiolysis studies of electron transfer in aqueous quinone solutions
WILLSON, R. L. (1971) · Transactions of the Faraday Society · doi:10.1039/tf9716703020 · Cited by 102
Soluble & membrane-bound superoxide dismutases in a blue-green alga (spirulina) and spinach
Lumsden, J., & Hall, D. O. (1974) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(74)90887-0 · Cited by 75
The Tiron free radical as a sensitive indicator of chloroplastic photoautoxidation
Miller, R. W., & Macdowall, F. D. H. (1975) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(75)90062-6 · Cited by 69
Self-citation
Purification of Superoxide Dismutase From Fungi and Characterization of the Reaction of the Enzyme with Catechols by Electron Spin Resonance Spectroscopy
Rapp, U., Adams, W. C., & Miller, R. W. (1973) · Canadian Journal of Biochemistry · doi:10.1139/o73-021 · Cited by 54
Self-citation
Comparison between the electron transfer reactions from free radicals and their corresponding peroxy radicals to quinones
Simic, M. G., & Hayon, E. (1973) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(73)90849-8 · Cited by 53
The Oxidation of Catechols by Reduced Flavins and Dehydrogenases
Miller, R. W., & Rapp, U. (1973) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)43512-6 · Cited by 45
Self-citation
Design considerations for nanosecond pulse radiolysis studies using kinetic spectrophotometry
HUNT, J. W., Greenstock, C. L., & Bronskill, M. J. (1972) · International Journal for Radiation Physics and Chemistry · doi:10.1016/0020-7055(72)90011-3 · Cited by 40
Self-citation

Show all 12 references

Research works printed but not linked: 1

Adams, 1968, Vol. 1, 289

Sorted by citations

Superoxide radical and superoxide dismutases
Fridovich, I. (1995) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.64.070195.000525 · Cited by 3,455
Superoxide Anion Chemistry—Its Role at the Core of the Innate Immunity
Andrés, C. M. C., Pérez de la Lastra, J. M., Andrés Juan, C., Plou, F. J., & Pérez-Lebeña, E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24031841 · Cited by 342
Manganese, superoxide dismutase, and oxygen tolerance in some lactic acid bacteria
Archibald, F. S., & Fridovich, I. (1981) · Journal of Bacteriology · doi:10.1128/jb.146.3.928-936.1981 · Cited by 319
Determination of main species involved in the first steps of TiO2 photocatalytic degradation of organics with the use of scavengers: The case of ofloxacin
Rodrı́guez, E. M., Márquez, G., Tena, M., Álvarez, P. M., & Beltrán, F. J. (2014) · Applied Catalysis B: Environmental · doi:10.1016/j.apcatb.2014.11.002 · Cited by 274
NOX5 NAD(P)H oxidase regulates growth and apoptosis in DU 145 prostate cancer cells
Brar, S. S., Corbin, Z. A., Kennedy, T. P., Hemendinger, R. A., Thornton, L., Bommarius, B., Arnold, R. S., Whorton, A. R., Sturrock, A., Huecksteadt, T. P., et al. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00525.2002 · Cited by 262
DNA Damage Induced by Methylated Trivalent Arsenicals Is Mediated by Reactive Oxygen Species
Nesnow, S., Roop, B. C., Lambert, G. R., Kadiiska, M. B., Mason, R. P., Cullen, W., & Mass, M. J. (2002) · Chemical Research in Toxicology · doi:10.1021/tx025598y · Cited by 251
Changes in superoxide radical and lipid peroxide formation in the brain, heart and liver during the lifetime of the rat
Sawada, M., & Carlson, J. C. (1987) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(87)90057-1 · Cited by 238
Formation of hydrogen peroxide and nitric oxide in rat skeletal muscle cells during contractions
Silveira, L. R., Pereira-da-Silva, L., Juel, C., & Hellsten, Y. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(03)00271-5 · Cited by 208
The Toxicology of Molecular Oxygen
Diguiseppi, J., Fridovich, I., & McCord, J. M. (1984) · Critical Reviews in Toxicology · doi:10.3109/10408448409044213 · Cited by 205
Intra- and extracellular measurement of reactive oxygen species produced during heat stress in diaphragm muscle
Zuo, L., Christofi, F. L., Wright, V. P., Liu, C. Y., Merola, A. J., Berliner, L. J., & Clanton, T. L. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.279.4.c1058 · Cited by 180
Activated oxygen species and oxidation of food constituents
Korycka-Dahl, M., Richardson, T., & Foote, C. S. (1978) · C R C Critical Reviews in Food Science and Nutrition · doi:10.1080/10408397809527250 · Cited by 170
Breakdown of photosynthetic pigments and lipids in spinach leaves with ozone fumigation: Role of active oxygens
Sakaki, T., Kondo, N., & Sugahara, K. (1983) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1983.tb06566.x · Cited by 165
Oxygen‐derived free radicals mediate endothelium‐dependent contractions to acetylcholine in aortas from spontaneously hypertensive rats
Yang, D., Félétou, M., Boulanger, C. M., Wu, H., Levens, N. R., Zhang, J., & Vanhoutte, P. M. (2002) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0704669 · Cited by 162
The Role of Heme and the Mitochondrion in the Chemical and Molecular Mechanisms of Mammalian Cell Death Induced by the Artemisinin Antimalarials
Chadwick, A. E., Copple, I. M., Maggs, J. L., O’Neill, P. M., & Park, B. K. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.144188 · Cited by 163
Effect of electron transfer inhibitors on superoxide generation in the cytochrome bc1 site of the mitochondrial respiratory chain
Ksenzenko, M. Y., Konstantinov, A. A., Khomutov, G. B., Tikhonov, A. N., & Ruuge, E. K. (1983) · FEBS Letters · doi:10.1016/0014-5793(83)80200-2 · Cited by 160
Cell permeable ROS scavengers, Tiron and Tempol, rescue PC12 cell death caused by pyrogallol or hypoxia/reoxygenation
Yamada, J., Yoshimura, S., Yamakawa, H., Sawada, M., Nakagawa, M., Hara, S., Kaku, Y., Iwama, T., Naganawa, T., Banno, Y., et al. (2002) · Neuroscience Research · doi:10.1016/s0168-0102(02)00196-7 · Cited by 143
The basis of color in muscle foods
Giddings, G. G., & SOLBERG, M. (1977) · C R C Critical Reviews in Food Science and Nutrition · doi:10.1080/10408397709527231 · Cited by 137
A method for the detection of superoxide in biological systems
Rosen, G. M., Finkelstein, E., & Rauckman, E. J. (1982) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(82)90097-2 · Cited by 137
Photosynthetic electron flow to oxygen and diffusion of hydrogen peroxide through the chloroplast envelope via aquaporins
Borisova‐Mubarakshina, M. M., Kozuleva, M. A., Rudenko, N. N., Naydov, I. A., Klenina, I. B., & Ivanov, B. N. (2012) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.02.036 · Cited by 132
Antibody-induced nonapoptotic cell death in human lymphoma and leukemia cells is mediated through a novel reactive oxygen species-dependent pathway
Honeychurch, J., Alduaij, W., Azizyan, M., Cheadle, E. J., Pelicano, H., Ivanov, A., Huang, P., Cragg, M. S., & Illidge, T. (2012) · Blood · doi:10.1182/blood-2011-12-395541 · Cited by 131
Site-specific DNA damage caused by lipid peroxidation products
Ueda, K., Kobayashi, S., Morita, J., & Komano, T. (1985) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/0167-4781(85)90041-7 · Cited by 125
Antioxidants protect rat diaphragmatic muscle function under hypoxic conditions
Mohanraj, P., Merola, A. J., Wright, V. P., & Clanton, T. L. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.84.6.1960 · Cited by 119
NO restores HIF-1α hydroxylation during hypoxia: Role of reactive oxygen species
Callapina, M., Zhou, J., Schmid, T., Köhl, R., & Brüne, B. (2005) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.05.009 · Cited by 118
Rapid Plasma Membrane Changes in Superoxide Radical Formation, Fluidity, and Phospholipase A2Activity in the Corpus Luteum of the Rat During Induction of Luteolysis*
Sawada, M., & Carlson, J. C. (1991) · Endocrinology · doi:10.1210/endo-128-6-2992 · Cited by 116
Confirmation of Superoxide Generation via Xanthine Oxidase in Streptozotocin-induced Diabetic Mice
Matsumoto, S., Koshiishi, I., Inoguchi, T., Nawata, H., & Utsumi, H. (2003) · Free Radical Research · doi:10.1080/1071576031000107344 · Cited by 112
The catecholic metal sequestering agent 1,2-dihydroxybenzene-3,5-disulfonate confers protection against oxidative cell damage
Krishna, C. M., Liebmann, J. E., Kaufman, D., DeGraff, W., Hahn, S. M., McMurry, T., Mitchell, J. B., & Russo, A. (1992) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(92)90142-j · Cited by 110
Highly stable UiO-66-NH2 by the microwave-assisted synthesis for solar photocatalytic water treatment
Solís, R. R., Peñas‐Garzón, M., Belver, C., Rodriguez, J. J., & Bedia, J. (2021) · Journal of environmental chemical engineering · doi:10.1016/j.jece.2021.107122 · Cited by 107
Superoxide generation by the respiratory chain of tumor mitochondria
Konstantinov, A. A., Peskin, A. V., Popova, E. Y., Khomutov, G. B., & Ruuge, E. K. (1987) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(87)90206-4 · Cited by 103
Vanadate-stimulated NADH oxidation in plasma membrane
Ramasarma, T., MacKellar, W. C., & Crane, F. L. (1981) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(81)90275-3 · Cited by 103
Oxidative degradation of glucose adducts to protein. Formation of 3-(N epsilon-lysino)-lactic acid from model compounds and glycated proteins.
Ahmed, M., Dunn, J. A., Walla, M. D., Thorpe, S. R., & Baynes, J. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)68379-6 · Cited by 100
Hydroxylated metabolites of the antimalarial drug primaquine. Oxidation and redox cycling.
Vasquez-Vivar, J. M., & Augusto, O. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50504-x · Cited by 92
Kinetics of Glycoxidation of Bovine Serum Albumin by Methylglyoxal and Glyoxal and its Prevention by Various Compounds
Sadowska‐Bartosz, I., Galiniak, S., & Bartosz, G. (2014) · Molecules · doi:10.3390/molecules19044880 · Cited by 91
Superoxide radical production by microsomal membranes from senescing carnation flowers: an effect on membrane fluidity
Mayak, S., Legge, R. L., & Thompson, J. E. (1983) · Phytochemistry · doi:10.1016/s0031-9422(00)84018-2 · Cited by 87
Anesthetic Preconditioning Improves Adenosine Triphosphate Synthesis and Reduces Reactive Oxygen Species Formation in Mitochondria after Ischemia by a Redox Dependent Mechanism
Novalija, E., Kevin, L. G., Eells, J. T., Henry, M. M., & Stowe, D. F. (2003) · Anesthesiology · doi:10.1097/00000542-200305000-00018 · Cited by 85
Effects of Co-administration of Antioxidants and Arsenicals on the Rat Urinary Bladder Epithelium
Wei, M. (2004) · Toxicological Sciences · doi:10.1093/toxsci/kfi033 · Cited by 83
Supported TiO2 solar photocatalysis at semi‐pilot scale: degradation of pesticides found in citrus processing industry wastewater, reactivity and influence of photogenerated species
Jiménez-Tototzintle, M., Maldonado, M. I., Rodrı́guez, E. M., Hernández‐Ramírez, A., Saggioro, E. M., Carra, I., & Pérez, J. A. S. (2013) · Journal of Chemical Technology & Biotechnology · doi:10.1002/jctb.4299 · Cited by 82
Oxygen evolution from hydrogen peroxide in photosystem II: flash-induced catalytic activity of water-oxidizing photosystem II membranes
Mano, J., Takahashi, M., & Asada, K. (1987) · Biochemistry · doi:10.1021/bi00383a014 · Cited by 82
DETECTION OF OXYGEN RADICALS IN BIOLOGICAL REACTIONS
Bors, W., Sarán, M., Lengfelder, E., Michel, C., Fuchs, C., & Frenzel, C. (1978) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1978.tb06982.x · Cited by 80
Conditional knockout of Mn-SOD targeted to type IIB skeletal muscle fibers increases oxidative stress and is sufficient to alter aerobic exercise capacity
Lustgarten, M. S., Jang, Y. C., Liu, Y., Müller, F. L., Qi, W., Steinhelper, M. E., Brooks, S. V., Larkin, L. M., Shimizu, T., Shirasawa, T., et al. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00372.2009 · Cited by 79
Hyperthermia induces injury to the intestinal mucosa in the mouse: evidence for an oxidative stress mechanism
Oliver, S. R., Phillips, N. A., Novosad, V. L., Bakos, M. P., Talbert, E. E., & Clanton, T. L. (2012) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00595.2011 · Cited by 74
2-Methoxyestradiol Does Not Inhibit Superoxide Dismutase
Kachadourian, R., Liochev, S. I., Cabelli, D. E., Patel, M. N., Fridovich, I., & Day, B. J. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2455 · Cited by 73
Superoxide Radical and Superoxide Dismutases
Fridovich, I. (1981) · Topics in environmental physiology and medicine · doi:10.1007/978-1-4612-5890-2_13 · Cited by 72
N-Demethylation reactions catalyzed by chloroperoxidase.
Kedderis, G. L., Koop, D. R., & Hollenberg, P. F. (1980) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)70444-x · Cited by 69
Carbonyl cyanide p-(trifluoromethoxy) phenylhydrazone (FCCP) as an O2− generator induces apoptosis via the depletion of intracellular GSH contents in Calu-6 cells
Han, Y. H., Kim, S. H., Kim, S. Z., & Park, W. H. (2008) · Lung Cancer · doi:10.1016/j.lungcan.2008.05.005 · Cited by 70
Activation of peroxymonosulfate by phosphite: Kinetics and mechanism for the removal of organic pollutants
Peng, G., You, W., Zhou, W., Zhou, G., Qi, C., & Hu, Y. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.129016 · Cited by 66
The Basis of Quality in Muscle Foods THE BAStS OF COLOR IN MUSCLE FOODS
Giddings, G. G. (1977) · Journal of Food Science · doi:10.1111/j.1365-2621.1977.tb01484.x · Cited by 66
Characterization of the N-demethylation reactions catalyzed by horseradish peroxidase.
Kedderis, G. L., & Hollenberg, P. F. (1983) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)82038-9 · Cited by 65
Use of catalase and superoxide dismutase to assess the roles of hydrogen peroxide and superoxide in the TiO2 or ZnO photocatalytic destruction of 1,2-dimethoxybenzene in water
Amalric, L., Guillard, C., & Pichat, P. (1994) · Research on Chemical Intermediates · doi:10.1163/156856794x00234 · Cited by 65
Studies on the antioxidant properties of some phytoestrogens
Kładna, A., Berczyński, P., Kruk, I., Piechowska, T., & Aboul-Enein, H. Y. (2016) · Luminescence · doi:10.1002/bio.3091 · Cited by 64
Oxygen‐derived free radicals mediate endothelium‐dependent contractions in femoral arteries of rats with streptozotocin‐induced diabetes
Shi, Y., So, K., Man, R. Y. K., & Vanhoutte, P. M. (2007) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707439 · Cited by 58
Novel isoreticular UiO-66-NH2 frameworks by N-cycloalkyl functionalization of the 2-aminoterephtalate linker with enhanced solar photocatalytic degradation of acetaminophen
Gómez‐Avilés, A., Solís, R. R., García‐Frutos, E. M., Bedia, J., & Belver, C. (2023) · Chemical Engineering Journal · doi:10.1016/j.cej.2023.141889 · Cited by 56
Initiation of Oxidative Changes in Foods
Korycka-Dahl, M., & Richardson, T. (1980) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(80)83064-5 · Cited by 54
Increased superoxide radical production evokes inducible DNA repair in Escherichia coli.
Brawn, M. K., & Fridovich, I. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)71187-7 · Cited by 53
The mechanism of deoxyribonucleic acid breakage induced by 4'-(9-acridinylamino)methanesulfon-m-anisidine and copper: role for cuprous ion and oxygen free radicals
Wong, A., Huang, C. H., & Crooke, S. T. (1984) · Biochemistry · doi:10.1021/bi00308a015 · Cited by 53
Reactivity of pyruvic acid and its derivatives towards reactive oxygen species
Kładna, A., Marchlewicz, M., Piechowska, T., Kruk, I., & Aboul-Enein, H. Y. (2015) · Luminescence · doi:10.1002/bio.2879 · Cited by 51
Inhibition of copper/zinc superoxide dismutase impairs NO ⋅-mediated endothelium-dependent relaxations
Wambi-Kiéssé, C. O., & Katušić, Z. S. (1999) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1999.276.3.h1043 · Cited by 49
The role of membrane-bound porphyrin-type compound as endogenous sensitizer in photodynamic damage to yeast plasma membranes
Fraikin, G. Y., Strakhovskaya, M. G., & Rubin, A. B. (1996) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/1011-1344(96)07287-9 · Cited by 47
Synergistic effect of graphitic-like carbon nitride and sulfur-based thiazole-linked organic polymer heterostructures for boosting the photocatalytic degradation of pharmaceuticals in water
Zandipak, R., Bahramifar, N., Torabi, M., Calero, M., Muñoz‐Batista, M. J., & Solís, R. R. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.152843 · Cited by 46
Reactive Oxygen Species in the Paraventricular Nucleus Mediate the Cardiac Sympathetic Afferent Reflex in Chronic Heart Failure Rats
Han, Y., Shi, Z., Zhang, F., Yang, Y., Zhong, M., Gao, X., Wang, W., & Zhu, G. (2007) · European Journal of Heart Failure · doi:10.1016/j.ejheart.2007.07.004 · Cited by 46
What is Unique About Superoxide Toxicity as Compared to Other Biological Reductants? — A Hypothesis
Czapski, G., Goldstein, S., & Meyerstein, D. (1988) · Free Radical Research Communications · doi:10.3109/10715768809055147 · Cited by 44
Production of superoxide in chloroplast thylakoid membranes
Kozuleva, M. A., Klenina, I. B., Proskuryakov, I. I., Kirilyuk, I. A., & Ivanov, B. N. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.03.004 · Cited by 43
Inhibition of nitrate reductase by azide in microalgae results in triglycerides accumulation
Zalogin, T. R., & Pick, U. (2013) · Algal Research · doi:10.1016/j.algal.2013.11.018 · Cited by 41
Sulfite-Induced Lipid Peroxidation in Chloroplasts as Determined by Ethane Production
Peiser, G. D., Lizada, M. C. C., & Yang, S. F. (1982) · PLANT PHYSIOLOGY · doi:10.1104/pp.70.4.994 · Cited by 41
Activation of NAD(P)H oxidase by outward movements of H+ ions in renal medullary thick ascending limb of Henle
Li, N., Zhang, G., Yi, F.-X., Zou, A.-P., & Li, P. (2005) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00416.2004 · Cited by 41
Superoxide scavengers augment contractile but not energetic responses to hypoxia in rat diaphragm
Wright, V. P., Klawitter, P. F., Iscru, D. F., Merola, A. J., & Clanton, T. L. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01022.2004 · Cited by 40
Pulse-radiolytic investigations of catechols and catecholamines II. Reactions of Tiron with oxygen radical species
Bors, W. (1979) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(79)90145-4 · Cited by 38
Photooxidation of arsenite by natural goethite in suspended solution
Wang, Y., Xu, J., Zhao, Y., Zhang, L., Xiao, M., & Wu, F. (2012) · Environmental Science and Pollution Research · doi:10.1007/s11356-012-1079-6 · Cited by 36
Suppression of Arsenic Trioxide-induced Apoptosis in HeLa Cells by N-Acetylcysteine
Han, Y. H., Kim, S. Z., Kim, S. H., & Park, W. H. (2008) · Molecules and Cells · doi:10.1016/s1016-8478(23)13958-6 · Cited by 36
Iron(III) binding in DNA solutions: Complex formation and catalytic activity in the oxidation of hydrazine derivatives
Netto, L. E. S., Ferreira, A. M. D. C., & Augusto, O. (1991) · Chemico-Biological Interactions · doi:10.1016/0009-2797(91)90048-c · Cited by 36
The changes of intracellular H2O2 are an important factor maintaining mitochondria membrane potential of antimycin A-treated As4.1 juxtaglomerular cells
Han, Y. W., Kim, S. Z., Kim, S. H., & Park, W. H. (2006) · Biochemical Pharmacology · doi:10.1016/j.bcp.2006.11.017 · Cited by 36
Epidermal growth factor potentiates EGFR(Y992/1173)-mediated therapeutic response of triple negative breast cancer cells to cold atmospheric plasma-activated medium
Wang, P., Zhou, R., Zhou, R., Feng, S., Zhao, L., Li, W., Lin, J., Rajapakse, A., Lee, C., Furnari, F. B., et al. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102976 · Cited by 34
Differential effects of Bcl-2 and caspases on mitochondrial permeabilization during endogenous or exogenous reactive oxygen species-induced cell death
Rincheval, V., Bergeaud, M., Mathieu, L., Leroy, J., Guillaume, A., Mignotte, B., Floch, N. L., & Vayssière, J. (2012) · Cell Biology and Toxicology · doi:10.1007/s10565-012-9219-9 · Cited by 34
Ruthenium deposited onto graphitic carbon modified with boron for the intensified photocatalytic production of benzaldehyde
Solís, R. R., Quintana, M. A., Blázquez, G., Calero, M., & Muñoz‐Batista, M. J. (2023) · Catalysis Today · doi:10.1016/j.cattod.2023.114266 · Cited by 33
Enzymic formation of glycolate in Chromatium. Role of superoxide radical in a transketolase-type mechanism
Asami, S., & Akazawa, T. (1977) · Biochemistry · doi:10.1021/bi00629a025 · Cited by 33
Superoxide radical production by sponges Sycon sp
Peskin, A. V., Labas, Y. A., & Tikhonov, A. N. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00981-8 · Cited by 32
Superoxide radicals are not the main promoters of acceptor-side-induced photoinhibitory damage in spinach thylakoids
Hideg, �., Spetea, C., & Vass, I. (1995) · Photosynthesis Research · doi:10.1007/bf00032294 · Cited by 32
Chlorophyll Destruction by the Bisulfite-Oxygen System
Peiser, G. D., & Yang, S. F. (1977) · PLANT PHYSIOLOGY · doi:10.1104/pp.60.2.277 · Cited by 32
Bleomycin may be activated for DNA cleavage by NADPH-cytochrome P-450 reductase
Kilkuskie, R. E., Macdonald, T. L., & Hecht, S. M. (1984) · Biochemistry · doi:10.1021/bi00320a042 · Cited by 32
Roles of superoxide anion and hydrogen peroxide during replication of two unrelated plant RNA viruses in Nicotiana benthamiana
Hyodo, K., Suzuki, N., Mise, K., & Okuno, T. (2017) · Plant Signaling & Behavior · doi:10.1080/15592324.2017.1338223 · Cited by 31
Reactive oxygen species generated during myocardial ischemia enable energetic recovery during reperfusion
Klawitter, P. F., Murray, H. N., Clanton, T. L., & Angelos, M. G. (2002) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00041.2002 · Cited by 30
Inhibitors of superoxide dismutases: A cautionary tale
Hassan, H. M., Dougherty, H. W., & Fridovich, I. (1980) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(80)90290-8 · Cited by 30
Synthesis of an Environmentally Friendly Modified Mulberry Branch-Derived Biochar Composite: High Degradation Efficiency of BPA and Mitigation of Toxicity in Silkworm Larvae
Qu, H., Chen, L., Yang, F., Zhu, J., Qi, C., & Peng, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043609 · Cited by 29
Dermatophagoides pteronyssinus 2regulates nerve growth factor release to induce airway inflammation via a reactive oxygen species-dependent pathway
Ye, Y.-L., Wu, H., Lin, C., Hsieh, C.-Y., Wang, J., Liu, F.-H., Ma, C.-T., Bei, C.-H., Cheng, Y.-L., Chen, C.-C., et al. (2010) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00165.2010 · Cited by 29
Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
Kozuleva, M. A., Klenina, I. B., Mysin, I. E., Kirilyuk, I. A., Opanasenko, V. K., Proskuryakov, I. I., & Ivanov, B. N. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.08.016 · Cited by 29
Superoxide Scavengers Improve Rat Pharyngeal Dilator Muscle Performance
Skelly, J. R., Bradford, A., Jones, J. F. X., & O’Halloran, K. D. (2009) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2009-0160oc · Cited by 29
Inactivation of bacteriophage øX174 by mitomycin C in the presence of sodium hydrosulfite and cupric ions
Ueda, K., Morita, J., Yamashita, K., & Komano, T. (1980) · Chemico-Biological Interactions · doi:10.1016/0009-2797(80)90029-0 · Cited by 29
Biochemical changes associated with the mechanism controlling superoxide radical formation in the aging rotifer
Sawada, M., & Carlson, J. C. (1990) · Journal of Cellular Biochemistry · doi:10.1002/jcb.240440304 · Cited by 29
Photooxidation of arsenic(III) to arsenic(V) on the surface of kaolinite clay
Ding, W., Wang, Y., Yu, Y., Zhang, X., Li, J., & Wu, F. (2015) · Journal of Environmental Sciences · doi:10.1016/j.jes.2015.03.017 · Cited by 28
Solar CPC pilot plant photocatalytic degradation of bisphenol A in waters and wastewaters using suspended and supported-TiO2. Influence of photogenerated species
Saggioro, E. M., Oliveira, A. S., Pavesi, T., Jiménez-Tototzintle, M., Maldonado, M. I., Correia, F. V., & Moreira, J. C. (2014) · Environmental Science and Pollution Research · doi:10.1007/s11356-014-2723-0 · Cited by 28
Superoxide anions modulate the effects of angiotensin-(1–7) in the rostral ventrolateral medulla on cardiac sympathetic afferent reflex and sympathetic activity in rats
Li, P., Zhang, F., Zhou, Y., Cui, B., & Han, Y. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.07.048 · Cited by 27
Role of sulfhydryl-dependent dimerization of soluble guanylyl cyclase in relaxation of porcine coronary artery to nitric oxide
Zheng, X., Ying, L., Liu, J., Dou, D., He, Q., Leung, S. W. S., Man, R. Y. K., Vanhoutte, P. M., & Gao, Y. Q. (2011) · Cardiovascular Research · doi:10.1093/cvr/cvr016 · Cited by 27
Superoxide Formation in Cardiac Mitochondria and Effect of Phenolic Antioxidants
Dudylina, A. L., Ivanova, M. V., Шумаев, К. Б., & Ruuge, E. K. (2018) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-018-0857-2 · Cited by 27
Relationships between the effects of redox potential, α‐Thenoyltrifluoroacetone and malonate on O2− and H2O2 generation by submitochondrial particles in the presence of succinate and antimycin
Ksenzenko, M. Y., Konstantinov, A. A., Khomutov, G. B., Tikhonov, A. N., & Ruuge, E. K. (1984) · FEBS Letters · doi:10.1016/0014-5793(84)80579-7 · Cited by 25
Tyrosine nitration in blood vessels occurs with increasing nitric oxide concentration
Amirmansour, C., Vallance, P. J., & Bogle, R. (1999) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0702590 · Cited by 25
On the Question of Superoxide Toxicity and the Biological Function of Superoxide Dismutases
Fee, J. A. (1982) · Elsevier eBooks · doi:10.1016/b978-0-08-024421-1.50010-0 · Cited by 25
Dinitrosyl iron complexes: Formation and antiradical action in heart mitochondria
Шумаев, К. Б., Dudylina, A. L., Ivanova, M. V., Pugachenko, I. S., & Ruuge, E. K. (2018) · BioFactors · doi:10.1002/biof.1418 · Cited by 24
New insight into PFOS transformation pathways and the associated competitive inhibition with other perfluoroalkyl acids via photoelectrochemical processes using GOTiO2 film photoelectrodes
Yang, J.-S., Lai, W. W.-P., & Lin, A. Y. (2021) · Water Research · doi:10.1016/j.watres.2021.117805 · Cited by 23
Sulfonic grafted graphitic-like carbon nitride for the improved photocatalytic production of benzaldehyde in water
Quintana, M. A., Solís, R. R., Blázquez, G., Calero, M., & Muñoz‐Batista, M. J. (2024) · Applied Surface Science · doi:10.1016/j.apsusc.2024.159717 · Cited by 23
Differential effects of pharmacologically generated reactive oxygen species upon functional activity of epididymal mouse spermatozoa
Baiardi, G., Ruiz, R. D., de Cúneo, M. F., Ponce, A. A., Lacuara, J. L., & Vincent, L. (1997) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-75-3-173 · Cited by 23
Induction of single strand scission in bacteriophage .PHI.X174 replicative form I DNA by mitomycin C.
Ueda, K., Morita, J., & Komano, T. (1981) · The Journal of Antibiotics · doi:10.7164/antibiotics.34.317 · Cited by 23

Authors: Greenstock, C. L., & Miller, R. W.
Affiliations: Atomic Energy (Canada) (CA)
ORCID: Miller, R.W.
Venue: Biochimica et Biophysica Acta (BBA) - Bioenergetics
Publisher: Elsevier BV
Published: 1975-07
Volume: 396
Issue: 1
Pages: 11-16
ISSN: 0005-2728 (ISSN-L)
DOI: 10.1016/0005-2728(75)90184-x
OpenAlex: W2075937164
Cited by: 157
References: 12
Citations by year: 2026: 3 · 2025: 2 · 2024: 5 · 2023: 5 · 2022: 2 · 2021: 2 · 2020: 3 · 2019: 1 · 2018: 3 · 2017: 4 · 2016: 1 · 2015: 5 · 2014: 7 · 2013: 4 · 2012: 7
FWCI: 1.76
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Biochimica et Biophysica Acta (BBA) - Bioenergetics (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
Physical Sciences › Chemistry › Organic Chemistry › Free Radicals and Antioxidants
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Keywords: Tiron, superoxide, p-benzoquinone, vitamin C, hydrogen peroxide, chloroplasts, photosystem I, superoxide detection, pulse radiolysis, rate constants
MeSH terms: Benzenesulfonates, Chloroplasts, Kinetics, Mathematics, Oxidation-Reduction, Oxygen, Plants, Superoxides, Time Factors, 1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt, Triticum

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

The oxidation of tiron by superoxide anion. Kinetics of the reaction in aqueous solution and in chloroplasts

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks