The chemical mechanism of oxidative stress due to the non-transferrin-bound iron (NTBI)

Abstract

Plasma iron is normally bound to the iron transport protein transferrin, but there are some iron ions not associated with transferrin. The latter ions are generally termed as non-transferrin-bound iron (NTBI) or labile plasma iron. The NTBI has been thought to play an important role in iron-induced cell damage with resultant peroxidation of cell membrane lipids and other biomolecules, and such oxidative damage is implicated as an important contributor in the pathogenesis of cancer, cardiovascular disease, aging and other degenerative disorders, but little is understood about the chemical composition of NTBI and the origin of toxicity due to NTBI. In this review, we demonstrated the several chemical models for NTBI, and elucidated the chemical mechanism of iron toxicity due to NTBI in human body on the basis of my concept on the mechanism of oxygen activation in biological oxygenases. This has lead to the conclusion that 1) NTBI are divided into two groups, water-in-soluble and water-soluble ones, 2) some of the water-soluble NTBI react with oxygen or hydrogen peroxide, changing these molecules to those exhibiting the reactivity similar to singlet oxygen (1△g), and this is the main reason for NTBI to induce the oxidative stress, and 3) the responsibility of hydroxyl radical or free singlet oxygen is negligible as a “reactive oxygen species” in the human body. Based on the discussions described in this article we have proposed a new technique to prevent the oxidative damage due to NTBI. In order to achieve the purpose, we have synthesized the new superpolyphenols which contain more than 100 molecules of catechol derivative in one polymeric compound; these are sometimes water-insoluble, and in another cases, water-soluble. We have observed that some of these compounds can eliminate NTBI effectively from the plasma, and also some of these derivatives can remove hydrogen peroxide from the solution. Thus, we can hope that our new super-polyphenols should depress greatly the oxidative stress due to NTBI, which may be consistent with the facts that the Japanese tea catechins which contain polyphenols exhibit high preventing effects against lifestyle-related diseases, and that some polyphenols have been known to protect the pathogenesis of Alzheimer’s disease. We also discussed the antioxidative function by zinc(II) ion, which depresses the oxidative damage by NTBI by promoting the formation of iron deposition.

Share and Cite:

Nishida, Y. (2012) The chemical mechanism of oxidative stress due to the non-transferrin-bound iron (NTBI). Advances in Bioscience and Biotechnology, 3, 1076-1086. doi: 10.4236/abb.2012.327131.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] McCord, J.M. (1996) Effects of positive iron status at a cellular level. Nutrition Reviews, 54, 85-86. doi:10.1111/j.1753-4887.1996.tb03876.x
[2] Beutler, E., Hoffbrand, A.V. and Cook, J.D. (2003) Iron deficiency and overload. The American Society of Hematology, 2003, 40-61.
[3] Nishida, Y. (2004) Oxidative stress and neurodegeneration. Medical Hypotheses and Research, 1, 227-245.
[4] Harrison, P.M. and Arosio, P. (1996) The ferritin: Molecular properties, iron storage function and cellular regulation. Biochimica et Biophysica Acta, 1275, 161-203. doi:10.1016/0005-2728(96)00022-9
[5] Chasteen, N.D. and Harrison, P.M. (1999) Meneralization in ferritin: An efficient means of iron storage. Journal of Structural Biology, 126, 182-194. doi:10.1006/jsbi.1999.4118
[6] Dresow, B., Petersen, D., Fischer, R. and Nielson, P. (2008) Non-transferin-bound iron in plasma following administration of oral iron drugs. Biometals, 21, 273-276. doi:10.1007/s10534-007-9116-5
[7] Evans, R.W., Rafique, R., Zarea, A., Rapisarda, C., Cammack, R., Evans, P.J., Porter, J.B. and Hider, R.C. (2008) Nature of non-transferrin-bound iron: Studies on iron citrate compelxes and thelassemic sera. Journal of Biological Inorganic Chemistry, 13, 57-74. doi:10.1007/s00775-007-0297-8
[8] Hershko, C., Link, G., Konjin, A. and Cabantchik, Z.I. (2005) Objectives and mechanism of iron chelation therapy. Annals of the New York Academy of Sciences, 1054, 124-135. doi:10.1196/annals.1345.015
[9] Nishida, Y., Ito, S., Okuno, T. and Ohba, S. (1997) New insight into reaction of iron(III)-peroxide adduct with alkanes: An alternative model for cytochrome P-450 and methane monooxygenase. Zeitschrift fur Naturforschung, 52C, 615-622.
[10] Nishida, Y. (1998) Important role of substrate in activation of dioxygen in biological oxygenases. Trends in Inorganic Chemistry, 5, 89-103.
[11] Li, J.-L., Okada, S., Hamazaki, S., Ebina, Y. and Midorikawa, O. (1987) Nephrotoxicity and it prevention by vitamin E in ferric nitrilotriacetate-promoted lipid peroxidation. Biochimica et Biophysica Acta, 922, 28-33. doi:10.1016/0005-2760(87)90241-4
[12] Kawabata, T., Ma, Y., Yamadori, I. and Okada, S. (1997) Ironinduced apotosis in mouse renal proximal tubules after an injection of a renal carcinogen, iron-nitrilotriacetate. Carcinogenesis, 18, 1389-1398. doi:10.1093/carcin/18.7.1389
[13] Mizuno, R., Kawabata, T., Sutoh, Y., Nishida, Y. and Okada, S. (2006) Oxidative renal tubular injuries induced by amino-carboxylate-type iron(III) coordination compound as candidate renal carcinogens. Biometals, 19, 675-683. doi:10.1007/s10534-006-9004-4
[14] Halliwell, B. and Gutteridge, J.M.C. (1985) Free Radicals in Biology and Medicine, Oxford University Press, London.
[15] Nishida, Y., Goto, A., Akamatsu, T., Ohba, S., Fujita, T. and Okada, S. (1994) Iron chelates in biological systems: Its relevance to induction of pathogenesis of tissue damage and carcinogenesis. Chemistry Letters, 1994, 641-644. doi:10.1246/cl.1994.641
[16] Nishida, Y. and Ito, S. (1995) Structures and reactivity of several iron(III) complexes in the presence of hydrogen peroxide: Relevance to induction of tissue damage caused by iron(III) chelates in rats. Polyhedron, 14, 2301-2308. doi:10.1016/0277-5387(95)00109-6
[17] Nishida, Y. and Akamatsu, T. (1992) Formation of active oxygen species due to presence of binuclear iorn(III) compound. J. Act. Oxyg. Free Rad., 3, 376-383.
[18] Nishida, Y. and Takeuchi, M. (1987) Unique reactivity of peroxide ion trapped in binuclear iron(III) complex. Zeitschrift fur Naturforschung, 42b, 52-54.
[19] Nishino, S., Hosomi, H., Ohba, S., Matsushima, H., Tokii, T. and Nishida, Y. (1999) Selective dioxygenation of cyclohexane catalyzed by hydrogen peroxide and dinuclear iron(III) complexes with m-alkoxo bridge. Journal of the Chemical Society, Dalton Transactions, 1999, 1509-1515. doi:10.1039/a809725i
[20] Nishida, Y., Itoh, Y. and Satoh, T. (2007) Origin of renal proximal tubular injuries by Fe(III)-nta chelate. Zeitschrift fur Naturforschung, 62c, 608-612.
[21] Nishida, Y. (2009) Structural characteristics of iron(III) chelates to induce tissue damage and renal carcinoma; chemical origin of the iron toxicity. TCIMail, 141, 1-15.
[22] Lippard, S.J., Schugar, H. and Walling, C. (1967) The crystal and molecular structure of an oxo-bridged binuclear iron(III) compelx, [(Hedta)FeO(Hedta)]2-. Inorganic Chemistry, 6, 1825-1831. doi:10.1021/ic50056a015
[23] Okada, S., Minamiyama, Y., Hamazaki, S., Toyokuni, S. and Sotomatsu, A. (1993) Glutathione cycle dependency of ferric nitrilotriacetate-induced lipid peroxidation in mouse proximal renal tubules. Archives of Biochemistry and Biophysics, 301, 138-142. doi:10.1006/abbi.1993.1125
[24] Heath, S.L. and Powell, A.K. (1992) The trapping of iron hydroxide unit by the ligand “Heidi”: Two new hydroxo(oxo)iron chelates containing 19 and 17 iron atoms. Angewandte Chemie, International Edition in English, 31, 191-193. doi:10.1002/anie.199201911
[25] Nishino, S., Kunita, M., Kobayashi, T., Matsushima, H., Tokii, T. and Nishida, Y. (1999) Interaction between the peroxide adduct of binuclear iron(III) complex with (HTTP) anion and the sugar moiety of nucleosides. Zeitschrift fur Naturforschung, 54b, 1272-1276.
[26] Bates, G.W. and Schlabach, M.R. (1973) The reaction of ferric salts with transferrin. The Journal of Biological Chemistry, 248, 3228-3232.
[27] Nishida, Y. and Yamada, K. (1990) Lipoxygenase-like function of some binuclear iron(III) compounds. Journal of the Chemical Society, Dalton Transactions, 1990, 3639-3641. doi:10.1039/dt9900003639
[28] Nishida, Y., Takeuchi, M., Shimo, H. and Kida, S. (1985) Synthesis and reactivity of binuclear iron(III) complexes with ligands composed of two trident chelating groups. Inorganica Chimica Acta, 96, 115-120. doi:10.1016/S0020-1693(00)93746-0
[29] Nishida, Y., Nasu, M. and Akamatsu, T. (1992) Reaction between binuclear iron(III) compounds and DMPO. Journal of the Chemical Society, Chemical Communications, 1992, 93-94. doi:10.1039/c39920000093
[30] Gaeta, A. and Hider, R.C. (2005) The crucial role of metal ions in neurodegeneration: The basis for a promising therapeutic strategy. British Journal of Pharmacology, 146, 1041-1059.
[31] Bush, A.I. (2003) The metallobiology of Alzheimer’s disease. Trends in Neurosciences, 26, 207-214. doi:10.1016/S0166-2236(03)00067-5
[32] Satoh, T., Abe, K. and Nishida, (2012) Oxidase-like function by apotransferrin towards Manganese(III) chelates. International Journal of Chemistry, 4, 10-15. doi:10.5539/ijc.v4n3p10
[33] Yoshida, K., Kaneko, K., Miyajima, H., Tokuda, T., Nakamura, A., Kato, M. and Ikeda, S. (2000) Increased lipid peroxidation in the brains of aceruplasminemia patients. Journal of the Neurological Sciences, 175, 91-95. doi:10.1016/S0022-510X(00)00295-1
[34] Sutoh, Y., Okawamukai, Y., Nishino, S. and Nishida, Y. (2006) Structure of a new tetranuclear iron(III) complex with an oxo-bridge; factors to govern formation and stability of oxo-bridged iron(III) species in the L-subunit of ferritin. Zeitschrift fur Naturforschung, 61c, 149-154.
[35] Andersson, M.E., Hogbom, M., R.-Matthis, A., Andersson, K.K., Sjoberg, B. and Nortlund, P. (1999) The crystal structure of an azide complex of the differous R2 subunit of ribonucleotide reductase displays a novel carboxylate shift with important mechanistic implication for diiron-catalayzed oxygen activation. Journal of the American Chemical Society, 121, 2346-2352. doi:10.1021/ja982280c
[36] Baik, M., Newcome, M., Friesner, R.A. and Lippard, S.J. (2003) Mechanistic studies on the hydroxylation of methane by methane monooxygenase. Chemical Reviews, 103, 2385-2419. doi:10.1021/cr950244f
[37] Nishino, S., Takahashi, Y. and Nishida, Y. (2002) Important role of hydrogen peroxide for storing of iron ion in human L-subunit ferritin. Inorganic Chemistry Communications, 5, 609-611. doi:10.1016/S1387-7003(02)00509-9
[38] Kato, J., Fujikawa, K., Kanda, M., Fukuda, N., Sasaki, K., Takayama, T., Kobune, K., Takada, K., Takimoto, R., Hamada, H., Ikeda, T. and Niitsu, Y. (2001) A mutation, in the iron-responsive element of H-ferritin mRNA, causing autosomal dominant iron overload. The American Journal of Human Genetics, 69, 191-197. doi:10.1086/321261
[39] Levi, S., Girelli, D., Perrone, F., Pasti, M., Beaumont, C., Corrocher, R., Albertini, A. and Arosio, P. (1998) Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome. Blood, 91, 4180-4187.
[40] Curtis, A.R., Fey, C., Morris, C.M., Bindoff, L.A., Patrick, P.G., Chinnery, P.F., Coulthard, A., Jackson, M.J., Jackson, A.P., McHale, D.P., Hay, D., Barker, W.A., Markham, A.F., Bates, D., Curtis, A. and Burn, J. (2001) Mutation in the gene region encoding basal ganglia disease. Nature Genetics, 28, 350-354. doi:10.1038/ng571
[41] Kakuda, T., Suzuki, Y. and Ikeda, I. (2011) Prevent effect of Tea catechins against lifestyle-related disease. FFI Journal, 216, 346-355.
[42] Hider, R.C., Ma, Y., M.-Holgado, F., Gaeta, A. and Roy, S. (2008) Iron chelation as a potential therapy for neurode-gehetaive disease. Biochemical Society Transactions, 36, 1304-1308. doi:10.1042/BST0361304
[43] Okawamukai, Y., Sutoh, Y. and Nishida, Y. (2006) Deposition of iron(III) hydroxide on aggregations of several proteins. Synthesis and Reactivity in Inorganic and Metal-Organic, and Nano-Metal Chemistry, 36, 373-375.
[44] Nishino, S., Kobayashi, T., Matsushima, H., Tokii, T. and Nishida, Y. (2006) Enhanced nucleophilicity and depresssed electrophilicity of peroxide ion by zinc(II), Aluminum(III) and Lanthanum(III) ion. Zeitschrift fur Naturforschung, 56c, 138-143.
[45] Moccegiani, E., Bertoni-Freddari, C., Marcellini, F. and Malavolta, M. (2005) Brain, aging and neurodegeneration: Role of zinc ion availability. Progress in Neurobiology, 75, 367-390. doi:10.1016/j.pneurobio.2005.04.005
[46] Kayed. R., Head, E., Thompson, J.L., McIntire, T.M., Milton, S.C., Cotman, C.W. and Glabe, C.G. (2003) Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis. Science, 300, 486-489. doi:10.1126/science.1079469
[47] Klein, W.L., Stine, W.B. Jr. and Teplow, D.B. (2004) Small assemblies of unmodified amyloid b-protein are the proximate neurotoxin in Alzheimer’s disease. Neurobiology of Aging, 25, 569-580.
[48] Grabrucker, A.M., Roman, M. and Garner, C.C. (2011) Brain-delivery of zincions as potential treatement for neurological diseases: Mini review. Drug Delivery Letters, 1, 13-23. doi:10.2174/2210304x11101010013
[49] Haysishi, O. (2005) An odyssey with oxygen. Biochemical and Biophysical Research Communications, 338, 2-6. doi:10.1016/j.bbrc.2005.09.019
[50] Nishida, Y. (2011) The chemical process of oxidative stress by copper(II) and iron(III) ions in several neuro-degenerative disorders. Monatshefte für Chemie, 142, 375-384.

Copyright © 2024 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.