Uric acid-iron ion complexes. A new aspect of the antioxidant functions of uric acid
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In order to survive in an oxygen environment, aerobic organisms have developed numerous mechanisms to protect against oxygen radicals and singlet oxygen. One such mechanism, which appears to have attained particular significance during primate evolution, is the direct scavenging of oxygen radicals, singlet oxygen, oxo-haem oxidants and hydroperoxyl radicals by uric acid. In the present paper we demonstrate that another important ‘antioxidant’ property of uric acid is the ability to form stable co-ordination complexes with iron ions. Formation of urate-Fe3+ complexes dramatically inhibits Fe3+-catalysed ascorbate oxidation, as well as lipid peroxidation in liposomes and rat liver microsomal fraction. In contrast with antioxidant scavenger reactions, the inhibition of ascorbate oxidation and lipid peroxidation provided by urate's ability to bind iron ions does not involve urate oxidation. Association constants (Ka) for urate-iron ion complexes were determined by fluorescence-quenching techniques. The Ka for a 1:1 urate-Fe3+ complex was found to be 2.4 × 10(5), whereas the Ka for a 1:1 urate-Fe2+ complex was determined to be 1.9 × 10(4). Our experiments also revealed that urate can form a 2:1 complex with Fe3+ with an association constant for the second urate molecule (K'a) of approx. 4.5 × 10(5). From these data we estimate an overall stability constant (Ks approximately equal to Ka × K'a) for urate-Fe3+ complexes of approx. 1.1 × 10(11). Polarographic measurements revealed that (upon binding) urate decreases the reduction potential for the Fe2+/Fe3+ half-reaction from −0.77 V to −0.67 V. Thus urate slightly diminishes the oxidizing potential of Fe3+. The present results provide a mechanistic explanation for our previous report that urate protects ascorbate from oxidation in human blood. The almost saturating concentration of urate normally found in human plasma (up to 0.6 mM) represents 5-10 times the plasma ascorbate concentration, and is orders of magnitude higher than the ‘free’ iron ion concentration. These considerations point to the physiological significance of our findings.
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Gout is a disease of iron overload, and uric acid accumulation is in response to iron overload, with remission of gouty symptoms on depletion of iron by phlebotomy.
“There is considerable evidence that this too is a disease of iron overload, and that uric acid accumulation – as both an antioxidant and an iron chelator [1348] – is in response to the iron overload [1349,1350] and with highly beneficial remission of gouty symptoms occurring on depletion of iron by phlebotomy [1351].”
From Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases (2009) · cites this paper as [1348]
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[30] Microsomal lipid peroxidation
Buege, J. A., & Aust, S. D. (1978) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(78)52032-6 · Cited by 13,437 · see citing works
Ames, B. N., Cathcart, R., Schwiers, E., & Hochstein, P. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.11.6858 · Cited by 2,915 · see citing works
Self-citationElectrochemistry at Solid Electrodes
Adams, R. N. (1969) · Medical Entomology and Zoology · Cited by 1,296 · see citing works
Role of metals in oxygen radical reactions
Aust, S. D., Morehouse, L. A., & Thomas, C. E. (1985) · Journal of Free Radicals in Biology & Medicine · doi:10.1016/0748-5514(85)90025-x · Cited by 1,150 · see citing works
Liposome oxidation and erythrocyte lysis by enzymically generated superoxide and hydrogen peroxide.
Kellogg, E. W., & Fridovich, I. (1977) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)39909-x · Cited by 509 · see citing works
Ascorbic Acid: Chemistry, Metabolism, and Uses
(1982) · Advances in Chemistry · doi:10.1021/ba-1982-0200 · Cited by 458 · see citing works
Fluorescence of riboflavin and flavin-adenine dinucleotide
Weber, G. (1950) · Biochemical Journal · doi:10.1042/bj0470114 · Cited by 404 · see citing works
Albert, A. (1953) · Biochemical Journal · doi:10.1042/bj0540646 · Cited by 275 · see citing works
Chapter 4 Lipid Vesicles as Carriers for Introducing Biologically Active Materials into Cells
Poste, G. H., Papahadjopoulos, D., & Vail, W. J. (1976) · Methods in cell biology · doi:10.1016/s0091-679x(08)60468-9 · Cited by 133 · see citing works
Conservation of vitamin C by uric acid in blood
Sevanian, A., Davies, K. J. A., & Hochstein, P. E. (1985) · Journal of Free Radicals in Biology & Medicine · doi:10.1016/0748-5514(85)90015-7 · Cited by 125 · see citing works
Self-citationOn the Mechanism of Peroxidation of Uric Acids by Hemoproteins
Howell, R. R., & Wyngaarden, J. Β. (1960) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)64505-3 · Cited by 121 · see citing works
The dye-sensitized photooxidation of purine and pyrimidine derivatives
Simon, M. I., & Vunakis, H. V. (1964) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(64)90253-x · Cited by 117 · see citing works
Similar Functions of Uric Acid and Ascorbate in Man ?
Proctor, P. H. (1970) · Nature · doi:10.1038/228868a0 · Cited by 111 · see citing works
Matsushita, S., Ibuki, F., & Aoki, A. (1963) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(63)90253-4 · Cited by 68 · see citing works
Smith, R. C., & Lawing, L. F. (1983) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(83)90582-9 · Cited by 63 · see citing works
[19] Uric acid: Functions and determination
Hochstein, P., Hatch, L., & Sevanian, A. (1984) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(84)05022-9 · Cited by 44 · see citing works
Self-citationMutagenic activity of ascorbate in mammalian cell cultures
Rosin, M. P., San, R. H. C., & STICH, H. F. (1980) · Cancer Letters · doi:10.1016/0304-3835(80)90145-7 · Cited by 43 · see citing works
Mechanism of the inhibitory action of phenelzine on microsomal drug metabolism.
Muakkassah-Kelly, S. F., & Yang, W. (1981) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)32773-4 · Cited by 32 · see citing works
Self-citationMeasurement of uric acid, ascorbic acid, and related metabolites in biological fluids
Hatch, L., & Sevanian, A. (1984) · Analytical Biochemistry · doi:10.1016/0003-2697(84)90816-9 · Cited by 32 · see citing works
Self-citationEvidence for a direct interaction of l-ascorbate with rat liver DNA
Jamaluddin, M. A., Rajalakshmi, S., & Sarma, D. S. R. (1981) · Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis · doi:10.1016/0005-2787(81)90199-4 · Cited by 9 · see citing works
Flagged first, then by citations
Research works printed but not linked: 5
- Pryor, W. A. (ed.) (1981) Free Radicals in Biology, vols. 1-5, Academic Press, New York
- Ames, B. N., Cathcart, R., Schwiers, E. & Hochstein, P. (1981) Proc. Natl. Acad. Sci. U.S.A. 78, 6858-6862
- Weber, G. (1948) Trans. Faraday Soc. 44, 185-196
- Albert, A. (1973) Selective Toxicity, pp. 282-391, Chapman and Hall, London 18. Hatch, L. L. & Sevanian, A. (1984) Anal. Biochem. 138, 324-328
- Haber, R. & Weiss, J. J. (1934) Proc. R. Soc. London Ser. A 147, 332-351
Cited by
Sorted by citations
Role of Oxidative Modifications in Atherosclerosis
Stocker, R., & Keaney, J. F. (2004) · Physiological Reviews · doi:10.1152/physrev.00047.2003 · Cited by 2,611 · see citing works
Exercise-Induced Oxidative Stress: Cellular Mechanisms and Impact on Muscle Force Production
Powers, S. K., & Jackson, M. J. (2008) · Physiological Reviews · doi:10.1152/physrev.00031.2007 · Cited by 2,459 · see citing works
Method for the measurement of antioxidant activity in human fluids
Koraćević, D., Koracevic, G., Djordjevic, V., Andrejevic, S., & Cosic, V. (2001) · Journal of Clinical Pathology · doi:10.1136/jcp.54.5.356 · Cited by 1,986 · see citing works
Oxygen radicals and human disease
CROSS, C. E., HALLIWELL, B., BORISH, E. T., PRYOR, W. A., AMES, B. N., SAUL, R. L., McCORD, J. M., & HARMAN, D. (1987) · Annals of Internal Medicine · doi:10.7326/0003-4819-107-4-526 · Cited by 1,856 · see citing works
Is There a Pathogenetic Role for Uric Acid in Hypertension and Cardiovascular and Renal Disease?
Johnson, R. J., Kang, D., Feig, D. I., Kivlighn, S. D., Kanellis, J., Watanabe, S., Tuttle, K. R., Rodríguez‐Iturbe, B., Herrera-Acosta, J., & Mazzali, M. (2003) · Hypertension · doi:10.1161/01.hyp.0000069700.62727.c5 · Cited by 1,354 · see citing works
The antioxidants of human extracellular fluids
Halliwell, B. B., & Gutteridge, J. M. C. (1990) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(90)90510-6 · Cited by 1,338 · see citing works
The role of reactive oxygen and antioxidant species in periodontal tissue destruction
Chapple, I., & Matthews, J. B. (2007) · Periodontology 2000 · doi:10.1111/j.1600-0757.2006.00178.x · Cited by 954 · see citing works
How to Characterize a Biological Antioxidant
Halliwell, B. B. (1990) · Free Radical Research Communications · doi:10.3109/10715769009148569 · Cited by 931 · see citing works
Wayner, D. D. M., Burton, G. W., Ingold, K. U., Barclay, L. R. C., & Locke, S. J. (1987) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(87)90155-3 · Cited by 871 · see citing works
Uric acid transport and disease
So, A. K.-L., & Thorens, B. (2010) · Journal of Clinical Investigation · doi:10.1172/jci42344 · Cited by 863 · see citing works
Role of oxygen free radicals in cancer development
Dreher, D., & Junod, A. F. (1996) · European Journal of Cancer · doi:10.1016/0959-8049(95)00531-5 · Cited by 853 · see citing works
Protein damage and degradation by oxygen radicals. II. Modification of amino acids.
Davies, K. J. A., Delsignore, M. E., & Lin, S. W. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)48019-2 · Cited by 845 · see citing works
Self-citationTowards the physiological function of uric acid
Becker, B. F. (1993) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(93)90143-i · Cited by 832 · see citing works
Oxidative Stress: Relationship with Exercise and Training
Finaud, J., Lac, G., & Filaire, E. (2006) · Sports Medicine · doi:10.2165/00007256-200636040-00004 · Cited by 771 · see citing works
Antioxidants in relation to lipid peroxidation
Niki, E. (1987) · Chemistry and Physics of Lipids · doi:10.1016/0009-3084(87)90052-1 · Cited by 677 · see citing works
Antioxidant Therapy in Acute Central Nervous System Injury: Current State
Gilgun-Sherki, Y., Rosenbaum, Z., Melamed, E., & Offen, D. (2002) · Pharmacological Reviews · doi:10.1124/pr.54.2.271 · Cited by 568 · see citing works
The Molecular Physiology of Uric Acid Homeostasis
Mandal, A. K., & Mount, D. B. (2014) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021113-170343 · Cited by 561 · see citing works
Kell, D. B. (2009) · BMC Medical Genomics · doi:10.1186/1755-8794-2-2 · Cited by 554 · see citing works
Pulmonary Strategies of Antioxidant Defense
Heffner, J. E., & Repine, J. E. (1989) · American Review of Respiratory Disease · doi:10.1164/ajrccm/140.2.531 · Cited by 536 · see citing works
Reactive Oxygen Species: Impact on Skeletal Muscle
Powers, S. K., Ji, L. L., Kavazis, A. N., & Jackson, M. J. (2011) · Comprehensive physiology · doi:10.1002/cphy.c100054 · Cited by 509 · see citing works
Uric acid and cardiovascular disease
Ndrepepa, G. (2018) · Clinica Chimica Acta · doi:10.1016/j.cca.2018.05.046 · Cited by 503 · see citing works
Yehye, W. A., Rahman, N. A., Ariffin, A., Hamid, S. B. A., Alhadi, A. A., Kadir, F. A., & Yaeghoobi, M. (2015) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2015.06.026 · Cited by 496 · see citing works
Protein damage and degradation by oxygen radicals. IV. Degradation of denatured protein.
Davies, K. J. A., Lin, S. W., & Pacifici, R. E. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)48021-0 · Cited by 480 · see citing works
Self-citationUric acid and serum antioxidant capacity: a reaction to atherosclerosis?
Nieto, F. J., Iribarren, C., Gross, M. D., Comstock, G. W., & Cutler, R. G. (2000) · Atherosclerosis · doi:10.1016/s0021-9150(99)00214-2 · Cited by 478 · see citing works
Endogenous skeletal muscle antioxidants
Chan, K. M., Decker, E. A., & Feustman, C. (1994) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408399409527669 · Cited by 441 · see citing works
Davies, K. J. A., & Goldberg, A. L. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47552-7 · Cited by 412 · see citing works
Self-citationPlasma Urate and Risk of Parkinson's Disease
Weisskopf, M. G., O’Reilly, É. J., Chen, H., Schwarzschild, M. A., & Ascherio, A. (2007) · American Journal of Epidemiology · doi:10.1093/aje/kwm127 · Cited by 386 · see citing works
Uric acid and cardiovascular disease: A clinical review
Saito, Y., Tanaka, A., Node, K., & Kobayashi, Y. (2020) · Journal of Cardiology · doi:10.1016/j.jjcc.2020.12.013 · Cited by 381 · see citing works
Altered Uric Acid Levels and Disease States
Kutzing, M. K., & Firestein, B. L. (2007) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.129031 · Cited by 378 · see citing works
Oxygen free radicals and human disease
Martínez‐Cayuela, M. (1995) · Biochimie · doi:10.1016/0300-9084(96)88119-3 · Cited by 363 · see citing works
Jin, H., Kanthasamy, A., Ghosh, A., Anantharam, V., Kalyanaraman, B., & Kanthasamy, A. G. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.09.007 · Cited by 362 · see citing works
Urate as a Predictor of the Rate of Clinical Decline in Parkinson Disease
Ascherio, A. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.247 · Cited by 355 · see citing works
Uric Acid and Cardiovascular Disease: An Update From Molecular Mechanism to Clinical Perspective
Yu, W., & Cheng, J. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.582680 · Cited by 354 · see citing works
Serum Urate as a Predictor of Clinical and Radiographic Progression in Parkinson Disease
Schwarzschild, M. A. (2008) · Archives of Neurology · doi:10.1001/archneur.2008.65.6.nct70003 · Cited by 309 · see citing works
Uric Acid and the Risks of Kidney Failure and Death in Individuals With CKD
Srivastava, A., Kazé, A. D., McMullan, C. J., Isakova, T., & Waikar, S. S. (2017) · American Journal of Kidney Diseases · doi:10.1053/j.ajkd.2017.08.017 · Cited by 309 · see citing works
Ishizaka, N., Ishizaka, Y., Toda, E.-I., Nagai, R., & Yamakado, M. (2005) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000161274.87407.26 · Cited by 306 · see citing works
Serum uric acid levels and the risk of Parkinson disease
de Lau, L. M. L., Koudstaal, P. J., Albert Hofman, D., & Breteler, M. M. B. (2005) · Annals of Neurology · doi:10.1002/ana.20663 · Cited by 302 · see citing works
Systemic Uric Acid Administration Increases Serum Antioxidant Capacity in Healthy Volunteers
Waring, W. S., Webb, D. J., & Maxwell, S. R. J. (2001) · Journal of Cardiovascular Pharmacology · doi:10.1097/00005344-200109000-00005 · Cited by 291 · see citing works
Antioxidants, Redox Signaling, and Pathophysiology in Schizophrenia: An Integrative View
Yao, J. K., & Keshavan, M. S. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3603 · Cited by 285 · see citing works
Antioxidant behaviour of caffeine: Efficient scavenging of hydroxyl radicals
Shi, X., Dalal, N. S., & Jain, A. C. (1991) · Food and Chemical Toxicology · doi:10.1016/0278-6915(91)90056-d · Cited by 285 · see citing works
Intracellular proteolytic systems may function as secondary antioxidant defenses: An hypothesis
Davies, K. J. A. (1986) · Journal of Free Radicals in Biology & Medicine · doi:10.1016/s0748-5514(86)80066-6 · Cited by 276 · see citing works
Self-citationThe Role of Oxidative Stress in Hyperuricemia and Xanthine Oxidoreductase (XOR) Inhibitors
Liu, N., Xu, H., Sun, Q., Yu, X., Chen, W., Wei, H., Jiang, J., Xu, Y., & Lu, W. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/1470380 · Cited by 265 · see citing works
Prognostic Significance of Uric Acid Serum Concentration in Patients With Acute Ischemic Stroke
Chamorro, Á., Obach, V., Cervera, Á., Revilla, M., Deulofeu, R., & Aponte, J. H. (2002) · Stroke · doi:10.1161/hs0402.105927 · Cited by 260 · see citing works
Uric Acid as a CNS Antioxidant
Bowman, G. L., Shannon, J., Frei, B. B., Kaye, J. A., & Quinn, J. F. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-1330 · Cited by 259 · see citing works
Halliwell, B. B., Grootveld, M. C., & Gutteridge, J. M. C. (1988) · Methods of biochemical analysis · doi:10.1002/9780470110546.ch2 · Cited by 259 · see citing works
Kaur, H., & Halliwell, B. B. (1990) · Chemico-Biological Interactions · doi:10.1016/0009-2797(90)90006-9 · Cited by 254 · see citing works
1 Iron toxicity and oxygen radicals
Gutteridge, J. M. C., & Halliwell, B. B. (1989) · Baillière s Clinical Haematology · doi:10.1016/s0950-3536(89)80017-4 · Cited by 251 · see citing works
Hyperuricemia and endothelial function: From molecular background to clinical perspectives
Maruhashi, T., Hisatome, I., Kihara, Y., & Higashi, Y. (2018) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2018.10.007 · Cited by 249 · see citing works
Iron and free radical reactions: two aspects of antioxidant protection
Halliwell, B. B., & Gutteridge, J. M. C. (1986) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(86)90207-0 · Cited by 249 · see citing works
Inosine to Increase Serum and Cerebrospinal Fluid Urate in Parkinson Disease
Schwarzschild, M. A., Ascherio, A., Beal, M. F., Cudkowicz, M., Curhan, G. C., Hare, J. M., Hooper, D. C., Kieburtz, K. D., Macklin, E. A., Oakes, D., et al. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2013.5528 · Cited by 246 · see citing works
Uric acid in health and disease: From physiological functions to pathogenic mechanisms
Wen, S., Arakawa, H., & Tamai, I. (2024) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2024.108615 · Cited by 246 · see citing works
Shohami, E., Beit‐Yannai, E., Horowitz, M., & Kohen, R. (1997) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-199710000-00002 · Cited by 241 · see citing works
Electrochemical Detection of Uric Acid in Mixed and Clinical Samples: A Review
Lakshmi, D., Whitcombe, M. J., Davis, F., Sharma, P. S., & Prasad, B. B. (2011) · Electroanalysis · doi:10.1002/elan.201000525 · Cited by 239 · see citing works
Grootveld, M. C., & Halliwell, B. B. (1987) · Biochemical Journal · doi:10.1042/bj2430803 · Cited by 236 · see citing works
Free radical metabolite of uric acid.
Maples, K. R., & Mason, R. P. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)77933-2 · Cited by 223 · see citing works
Markey, C. M., Alward, A., Weller, P. E., & Marnett, L. J. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45564-0 · Cited by 214 · see citing works
Peroxidase Properties of Extracellular Superoxide Dismutase
Hink, H. U., Santanam, N., Dikalov, S., McCann, L. A., Nguyen, A. D., Parthasarathy, S., Harrison, D. G., & Fukai, T. (2002) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000027524.86752.02 · Cited by 201 · see citing works
Uric Acid and Hypertension: An Update With Recommendations
Sánchez‐Lozada, L. G., Rodríguez‐Iturbe, B., Kelley, E. E., Nakagawa, T., Madero, M., Feig, D. I., Borghi, C., Piani, F., Cara‐Fuentes, G., Bjornstad, P., et al. (2020) · American Journal of Hypertension · doi:10.1093/ajh/hpaa044 · Cited by 200 · see citing works
Plasma malondialdehyde (MDA) levels in breast and lung cancer patients
Gönenç, A., Özkan, Y., Torun, M., & Şimşek, B. (2001) · Journal of Clinical Pharmacy and Therapeutics · doi:10.1046/j.1365-2710.2001.00334.x · Cited by 197 · see citing works
Xanthine dehydrogenase/xanthine oxidase and oxidative stress
Chung, H. Y., Baek, B. S., Song, S. H., Kim, M. S., Huh, J. I., Shim, K. H., Kim, K. W., & Lee, K. H. (1997) · AGE · doi:10.1007/s11357-997-0012-2 · Cited by 194 · see citing works
Journal of Pharmaceutical and Biomedical Sciences
(2016) · Journal of Pharmaceutical and Biomedical Sciences · doi:10.20936/jpbms · Cited by 193 · see citing works
Oxidative stress tests: overview on reliability and use. Part I.
Palmieri, B., & Sblendorio, V. T. (2007) · PubMed · Cited by 181 · see citing works
U‐Shaped Association Between Serum Uric Acid Level and Risk of Mortality
Cho, S. K., Chang, Y., Kim, I., & Ryu, S. (2018) · Arthritis & Rheumatology · doi:10.1002/art.40472 · Cited by 178 · see citing works
Gout and risk of Parkinson disease
Alonso, Á., Rodríguez, L. A. G., Logroscino, G., & Hernán, M. Á. (2007) · Neurology · doi:10.1212/01.wnl.0000279518.10072.df · Cited by 165 · see citing works
Oxidative Stress, the Paradigm of Ozone Toxicity in Plants and Animals
Iriti, M., & Faoro, F. (2007) · Water Air & Soil Pollution · doi:10.1007/s11270-007-9517-7 · Cited by 157 · see citing works
Cardiovascular disease and nutrient antioxidants: Role of low‐density lipoprotein oxidation
Frei, B. B. (1995) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408399509527689 · Cited by 155 · see citing works
Uric acid is reduced in the substantia nigra in parkinson's disease: Effect on dopamine oxidation
Church, W. H., & Ward, V. L. (1994) · Brain Research Bulletin · doi:10.1016/0361-9230(94)90285-2 · Cited by 154 · see citing works
Iron, Plasma Antioxidants, and the 'Oxygen Radical Disease of Prematurity'
Sullivan, J. L. (1988) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.1988.02150120095048 · Cited by 152 · see citing works
Urate-null rosy mutants of Drosophila melanogaster are hypersensitive to oxygen stress.
Hilliker, A. J., Duyf, B., Evans, D. H., & Phillips, J. P. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4343 · Cited by 151 · see citing works
Gout and the risk of Alzheimer's disease: a population-based, BMI-matched cohort study
Lu, N., Dubreuil, M., Zhang, Y., Neogi, T., Rai, S. K., Ascherio, A., Hernán, M. Á., & Choi, H. K. (2015) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2014-206917 · Cited by 149 · see citing works
Uric Acid and Cognitive Function in Older Individuals
Tana, C., Ticinesi, A., Prati, B., Nouvenne, A., & Meschi, T. (2018) · Nutrients · doi:10.3390/nu10080975 · Cited by 149 · see citing works
Asymptomatic hyperuricemia: is it really asymptomatic?
Yip, K. H.-K., Cohen, R. E., & Pillinger, M. H. (2019) · Current Opinion in Rheumatology · doi:10.1097/bor.0000000000000679 · Cited by 146 · see citing works
Johnson, R. J., Sautin, Y. Y., Oliver, W. J., Roncal, C., Mu, W., Sánchez‐Lozada, L. G., Rodríguez‐Iturbe, B., Nakagawa, T., & Benner, S. A. (2008) · Journal of Comparative Physiology B · doi:10.1007/s00360-008-0291-7 · Cited by 145 · see citing works
Urate: A Novel Biomarker of Parkinson‘s Disease Risk, Diagnosis and Prognosis
Cipriani, S., Chen, X. M., & Schwarzschild, M. A. (2010) · Biomarkers in Medicine · doi:10.2217/bmm.10.94 · Cited by 142 · see citing works
Prospective study of plasma urate and risk of Parkinson disease in men and women
Gao, X., O’Reilly, É. J., Schwarzschild, M. A., & Ascherio, A. (2016) · Neurology · doi:10.1212/wnl.0000000000002351 · Cited by 142 · see citing works
Patterson, R. A., Horsley, E. T. M., & Leake, D. S. (2003) · Journal of Lipid Research · doi:10.1194/jlr.m200407-jlr200 · Cited by 142 · see citing works
The Promise of Neuroprotective Agents in Parkinson?s Disease
Seidl, S. E., & Potashkin, J. A. (2011) · Frontiers in Neurology · doi:10.3389/fneur.2011.00068 · Cited by 141 · see citing works
Low plasma uric acid level in Parkinson's disease
Annanmäki, T., Muuronen, A., & Murros, K. E. (2007) · Movement Disorders · doi:10.1002/mds.21502 · Cited by 141 · see citing works
Inhibition by Uric Acid of Free Radicals that Damage Biological Molecules
Muraoka, S., & Miura, T. (2003) · Pharmacology & Toxicology · doi:10.1111/j.1600-0773.2003.pto930606.x · Cited by 137 · see citing works
Andreadou, E., Nikolaou, C., Gournaras, F., Rentzos, M., Boufidou, F., Tsoutsou, A., Zournas, C., Zissimopoulos, V., & Vassilopoulos, D. (2009) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2009.06.012 · Cited by 137 · see citing works
Evidence for erythrocyte lipid peroxidation in acute falciparum malaria
Das, B. S., & Nanda, N. K. (1999) · Transactions of the Royal Society of Tropical Medicine and Hygiene · doi:10.1016/s0035-9203(99)90180-3 · Cited by 134 · see citing works
Low uric acid levels in serum of patients with ALS: Further evidence for oxidative stress?
Keizman, D., Ish‐Shalom, M., Berliner, S. A., Maimon, N., Vered, Y., Artamonov, I., Tsehori, J., Nefussy, B., & Drory, V. E. (2009) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2009.06.002 · Cited by 133 · see citing works
Targeting urate to reduce oxidative stress in Parkinson disease
Crotty, G. F., Ascherio, A., & Schwarzschild, M. A. (2017) · Experimental Neurology · doi:10.1016/j.expneurol.2017.06.017 · Cited by 131 · see citing works
The potential of probiotics in the amelioration of hyperuricemia
Zhao, H., Lu, Z., & Lu, Y. (2022) · Food & Function · doi:10.1039/d1fo03206b · Cited by 128 · see citing works
Uric acid in Parkinson's disease
Schlesinger, I., & Schlesinger, N. (2008) · Movement Disorders · doi:10.1002/mds.22139 · Cited by 127 · see citing works
Hu, L., Hu, G., Xu, B. P., Zhu, L., Zhou, W., Wang, T., Bao, H., & Cheng, X. (2019) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgz068 · Cited by 124 · see citing works
Uric Acid and the Origins of Hypertension
Feig, D. I., Madero, M., Jalal, D. I., Sánchez‐Lozada, L. G., & Johnson, R. J. (2013) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2012.12.078 · Cited by 124 · see citing works
Protein Oxidation in Aging Braina
Smith, C. D., Carney, J. M., TATSUMO, T., Stadtman, E. R., Floyd, R. A., & Markesbery, W. R. (1992) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1992.tb38654.x · Cited by 124 · see citing works
Renal effects of uric acid: hyperuricemia and hypouricemia
Park, J. H., Jo, Y. S., & Lee, J.-H. (2020) · The Korean Journal of Internal Medicine · doi:10.3904/kjim.2020.410 · Cited by 123 · see citing works
Mudway, I., Duggan, S. T., Venkataraman, C., Habib, G., Kelly, F. J., & Grigg, J. (2005) · Particle and Fibre Toxicology · doi:10.1186/1743-8977-2-6 · Cited by 122 · see citing works
Reduced level of plasma antioxidant uric acid in schizophrenia
Yao, J. K., Reddy, R. D., & van Kammen, D. P. (1998) · Psychiatry Research · doi:10.1016/s0165-1781(98)00051-1 · Cited by 121 · see citing works
Oxidants, nitrosants, and the lung
van der Vliet, A., & Cross, C. E. (2000) · The American Journal of Medicine · doi:10.1016/s0002-9343(00)00479-4 · Cited by 120 · see citing works
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese
Iwai, N., Mino, Y., Hosoyamada, M., Tago, N., Kokubo, Y., & Endou, H. (2004) · Kidney International · doi:10.1111/j.1523-1755.2004.00839.x · Cited by 118 · see citing works
Purine metabolism is dysregulated in patients with major depressive disorder
Ali-Sisto, T., Tolmunen, T., Toffol, E., Viinamäki, H. T., Mäntyselkä, P. T., Valkonen‐Korhonen, M., Honkalampi, K. M., Ruusunen, A. A., Velagapudi, V., & Lehto, S. M. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.04.017 · Cited by 117 · see citing works
Plasma Copper and Antioxidant Status in Wilson's Disease
Ogihara, H., Ogihara, T., Miki, M., Yasuda, H., & Mino, M. (1995) · Pediatric Research · doi:10.1203/00006450-199502000-00016 · Cited by 116 · see citing works
Purinergic signaling in the modulation of redox biology
Savio, L. E. B., Leite-Aguiar, R., Alves, V. S., Coutinho‐Silva, R., & Wyse, Â. T. D. S. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102137 · Cited by 113 · see citing works
Hong, Q., Qi, K., Feng, Z., Huang, Z., Cui, S., Wang, L., Fu, B., Ding, R., Yang, J., Chen, X., et al. (2012) · Cell Calcium · doi:10.1016/j.ceca.2012.01.003 · Cited by 110 · see citing works
Nutritional Risk Factors, Microbiota and Parkinson’s Disease: What Is the Current Evidence?
Boulos, C., Yaghi, N., El Hayeck, R., Heraoui, G. N., & Fakhoury-Sayegh, N. (2019) · Nutrients · doi:10.3390/nu11081896 · Cited by 109 · see citing works
Gong, L., Zhang, Q., Zhang, N., Hua, W., Huang, Y., Di, P., Huang, T., Xu, X., Liu, C., Hu, L., et al. (2012) · Journal of Neurochemistry · doi:10.1111/jnc.12038 · Cited by 107 · see citing works
Insulin-related metabolic changes during treatment with valproate in patients with epilepsy
Pylvänen, V., Pakarinen, A., Knip, M., & Isojärvi, J. I. T. (2006) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2006.02.008 · Cited by 107 · see citing works
- Authors
- Davies, K. J. A., Sevanian, A., Muakkassah-Kelly, S. F., & Hochstein, P.
- Affiliations
- University of Southern California (US)
- ORCID
- Davies, K J A
- Venue
- Biochemical Journal
- Publisher
- Portland Press Ltd.
- Published
- 1986-05-01
- Volume
- 235
- Issue
- 3
- Pages
- 747-754
- ISSN
- 0264-6021 (ISSN-L)
- 1470-8728
- PMC
- PMC1146751
- OpenAlex
- W1832537945
- Cited by
- 558
- References
- 20
- Citations by year
- 2026: 11 · 2025: 14 · 2024: 19 · 2023: 23 · 2022: 18 · 2021: 25 · 2020: 22 · 2019: 11 · 2018: 20 · 2017: 19 · 2016: 16 · 2015: 15 · 2014: 17 · 2013: 23 · 2012: 23
- FWCI
- 17.95
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Biochemical Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Environmental Health Sciences (ES-03785, ES03466, ES03598)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Free Radicals and Antioxidants
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Health Sciences › Medicine › Nephrology › Gout, Hyperuricemia, Uric Acid
- Keywords
- uric acid, antioxidant function, iron(III) coordination, ascorbic acid oxidation, lipid peroxidation, binding constant, oxygen free radicals, singlet oxygen
- MeSH terms
- Animals, Ascorbic Acid, Hydrogen-Ion Concentration, Iron, Liposomes, Male, Microsomes, Liver, Organometallic Compounds, Oxidation-Reduction, Rats, Inbred Strains, Uric Acid, Macromolecular Substances, Lipid Metabolism, Rats
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