Exposure to excess dissolved iron in vivo affects oxidative status in the bivalve Mya arenaria

Comparative Biochemistry and Physiology - C Toxicology and Pharmacology

Volumn 152, Issue 2, 2010, Pages 167-174

  González, Paula M ^a   Abele, Doris ^b   Puntarulo, Susana ^a  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

^b ALFRED WEGENER INSTITUTE FOR POLAR AND MARINE RESEARCH   (Germany)

Author keywords

Iron overload; Labile iron pool; Mya arenaria; Oxidative stress

Indexed keywords

ASCORBIC ACID; CATALASE; GLUTATHIONE; IRON; NITRATE; NITRIC OXIDE; NITRITE; REACTIVE OXYGEN METABOLITE; SEA WATER; SUPEROXIDE DISMUTASE; THIOBARBITURIC ACID REACTIVE SUBSTANCE;

AEROBIC METABOLISM; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; ELECTRON SPIN RESONANCE; ENZYME ACTIVITY; EXOCRINE GLAND; EXPOSURE; MORTALITY; MYA; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; SPIN TRAPPING;

ANIMALIA; BIVALVIA; MYA ARENARIA;

EID: 77952741241     PISSN: 15320456     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbpc.2010.04.006     Document Type: Article

References (48)

1. Abele D., Heise K., Pörtner H.O., and Puntarulo S. Temperature-dependence of mitochondrial function and production of reactive oxygen species in the intertidal mud clam Mya arenaria. J. Exp. Biol. 205 (2002) 1831-1841
2. Aebi H. Catalase in vitro. Methods Enzymol. 105 (1984) 121-126
3. Ahearn G.A., Mandal P.K., and Mandal A. Mechanisms of heavy-metal sequestration and detoxification in crustaceans: a review. J. Comp. Physiol. 174 6 (2004) 439-452
4. Alves de Almeida E., Miyamoto S., Celso Dias Bainy A., Gennari de Medeiros M.H., and Di Mascio P. Protective effect of phospholipid hydroperoxide glutathione peroxidase (PHGPx) agaist lipid peroxidation in mussels Perna perna exposed to different metals. Mar. Pollut. Bull. 49 (2004) 386-392
5. Boveris A. Biochemistry of free radicals: from electrons to tissues. Medicina 54 (1998) 350-356
6. Bralet J., Schreiber L., and Bouvier C. Effect of acidosis and anoxia on iron delocalization from brain homogenates. Biochem. Pharmacol. 43 5 (1992) 971-979
7. Cooper C.E. Nitric oxide and iron proteins. Biochim. Biophys. Acta 1411 (1999) 290-309
8. Darbari D., Loyevsky M., Gordeuk V., Kark J.A., Castro O., Rana S., Apprey V., and Kurantsin-Mills J. Fluorescence measurements of the labile iron pool of sickle erythrocytes. Blood 102 (2003) 357-364
9. Davis K.L., Martin E., Turko I.V., and Murad F. Novel effects of nitric oxide. Annu. Rev. Pharmacol. Toxicol. 41 (2001) 203-236
10. Dee G., Rice-Evans C., Obeyesekera S., Meraji S., Jacobs M., and Bruckdorfer K.R. The modulation of ferryl myoglobin formation and its oxidative effects on low density lipoproteins by nitric oxide. FEBS Lett. 294 (1991) 38-42
11. Estévez M.S., Malanga G., and Puntarulo S. Iron-dependent oxidative stress in Chlorella vulgaris. Plant Sci. 161 (2001) 9-17
12. Estévez M.S., Abele D., and Puntarulo S. Lipid radical generation in polar (Laternula elliptica) and temperate (Mya arenaria) bivalves. Comp. Biochem. Physiol. 132 B (2002) 729-737
13. Fariss M.W., and Reed D.J. High-performance liquid chromatography of thiols and disulfides: dinitrophenol derivatives. Meths Enzymol. 143 (1987) 101-109
14. Gallagher E.P., Canadá A.T., and DiGiulio R.T. The protective role of glutathione in chlorothalonil-induced toxicity to channel catfish. Aquat. Toxicol. 23 (1992) 155-168
15. Galleano M., Aimo L., and Puntarulo S. Ascorbyl radical / ascorbate ratio in plasma from iron overloaded rats as oxidative stress indicator. Toxicol. Lett. 133 (2002) 193-201
16. Geyer H., Sheehan P., Kotzias D., Freitag D., and Korte F. Prediction of ecotoxicological behaviour of chemicals: relationship between physico-chemical properties and bioaccumulation of organic chemicals in the mussel Mytilus edulis. Chemosphere 11 (1982) 1121-1134
17. Gisone P., Boveris A.D., Dubner D., Perez M.R., Robello E., and Puntarulo S. Early neuroprotective effect of nitric oxide in developing rat brain irradiated in utero. Neurotoxicology 24 (2003) 245-253
18. González P.M., Abele D., and Puntarulo S. Iron and radical content in Mya arenaria. Possible sources of NO generation. Aquat. Toxicol. 89 (2008) 122-128
19. González P.M., Malanga G., and Puntarulo S. Ferritin and labile iron pool in limpets from the Beagle Channel. In: Svensson E.P. (Ed). Aquatic Toxicology Research Focus 9 (2008), Nova Science Publishers Inc, New York 177-188
20. Gorbunov N.V., Osipov A.N., Day B.W., Zayas-Rivera B., Kagan V.E., and Elsayed N.M. Reduction of ferrylmyoglobin and ferrylhemoglobin by nitric oxide: a protective mechanism against ferryl hemoprotein-induced oxidations. Biochemistry 34 (1995) 6689-6699
21. Hering J., and Morel F. Kinetics of trace metal complexation: role of alkaline-earth metals. Environ. Sci. Technol. 22 (1988) 1469-1478
22. Hogg N., Kalyanaraman B., Joseph J., Struck A., and Parthasarathy S. Inhibition of low-density lipoprotein oxidation by nitric oxide. Potential role in atherogenesis. FEBS Lett. 334 (1993) 170-174
23. Kanner J., Harel S., and Granit R. Nitric oxide as an antioxidant. Arch. Biochem. Biophys. 289 (1991) 130-136
24. King D.W., Lounsbury H.A., and Millero F.J. Rates and mechanisms of Fe (II) oxidation at nanomolar total iron concentrations. Environ. Sci. Technol. 29 (1995) 818-824
25. Kotake Y., Tanigawa T., Tanigawa M., Ueno I., Randel Allen D., and Lai C.-S. Continuous monitoring of cellular nitric oxide generation by spin trapping with an iron-dithiocarbamate complex. Biochim. Biophys. Acta 1289 (1996) 362-368
26. Kozak R.G., Malanga G., Caro A., and Puntarulo S. Ascorbate free radical content in photosynthetic organisms alter exposure to ultraviolet-B. Rec. Res. Dev. Plant Physiol. 1 (1997) 233-239
27. Kutnink M.A., Hawkes W.C., Schaus E.E., and Omaye S.T. An internal standard method for the unattended high-performance liquid chromatographic analysis of ascorbic acid in blood components. Anal. Biochem. 166 (1987) 424-430
28. Livingstone D.R. Contaminant-stimulated reactive oxygen species production and oxidative damage in aquatic organisms. Mar. Pollut. Bull. 42 (2001) 656-666
29. Lowry O.H., Rosebrough N.J., Farr A.L., and Randall R.J. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193 (1951) 265-275
30. Malanga G., González P.M., Estévez M.S., Abele D., and Puntarulo S. Oxidative stress in Antarctic algae and molluscs. In: Wiencke C., Ferreyra G.A., Abele D., and Marenssi S. (Eds). The Antarctic ecosystem of Potter Cove, King-George Island (Isla 25 de Mayo) (2008), Bremerhaven, Germany 208-215
31. Malanga G., Pérez A., Calvo J., and Puntarulo S. The effect of seasonality on oxidative metabolism in the sea urchin Loxechinus albus. Mar. Biol. 156 (2009) 763-770
32. McCord J.M., and Fridovich I. Superoxide dismutase. Enzymatic function for erithrocuprein (hemocuprein). J. Biol. Chem. 244 (1969) 6019-6055
33. Pedersen J.Z., De Maria F., Turrella P., Federeci G., Mattei M., Fabrini R., Dawood K., Massimi M., Caccuri A.M., and Ricci G. Glutathione transferases sequester toxic dinitrosyl-iron complexes in cells. J. Biol. Chem. 282 (2007) 6364-6371
34. Pierre J.L., and Fontecave M. Iron and activated oxygen species in biology: the basic chemistry. Biometals 12 (1999) 195-199
35. 2 after metabolic inhibition by fluoride and nitrilotriacetic acid. Respir. Physiol. 81 (1990) 255-274
36. Puntarulo S., Estévez M.S., Malanga G., and Calvo J. Oxidative stress in invertebrates. In: Thatje S., Calcagno A., and Arntz W.E. (Eds). Evolution of the Antarctic Fauna. Extended Abstracts of the IBMANT/ANDEEP International Symposium and Workshop 2003 (2005) 80-82
37. Radi R., Rubbo H., and Freeman B.A. The double-edge action of nitric oxide on free radical mediated oxidations. Ciencia e Culture J. Braz. Assoc. Adv. Sci. 47 (1995) 288-296
38. 2 formation. FASEB J. 14 (2000) 1953-1964
39. Robello E., Galatro A., and Puntarulo S. Iron role in oxidative metabolism of soybean axes upon growth effect of iron overload. Plant Sci. 172 (2007) 939-947
40. Rubbo H., Radi R., Trujillo M., Telleri R., Kalyanaramann B., Barnes S., Kirk M., and Freeman B.A. Nitric oxide regulation of superoxide and peroxynitrite-dependent lipid peroxidation. Formation of novel nitrogen-containing oxidized lipid derivatives. J. Biol. Chem. 269 42 (1994) 26066-26075
41. Schafer F.Q., and Buettner G.R. Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple. J. Free Radic. Biol. Med. 30 (2001) 1191-1212
42. Sharpe M.A., Robb S.J., and Clark J.B. Nitric oxide and Fenton/Haber-Weiss chemistry: nitric oxide is a potent antioxidant at physiological concentrations. J. Neurochem. 87 2 (2003) 386-394
43. Storch D., Abele D., and Pörtner H.O. The effect of hydrogen peroxide on isolated body wall of the lugworm Arenicola marina at different extracellular pH levels. Comp. Biochem. Physiol. 128C (2001) 391-399
44. Templeton D.M., and Liu Y. Genetic regulation of cell function in response to iron overload or chelation. Biochim. Biophys. Acta 1619 2 (2003) 113-124
45. Tynan S., Eggins S., Kinsley L., Welch S.A., and Kirste D. Mussel shells as environmental tracers: an example from the loveday basin. In: Roach I.C. (Ed). Ten years of CRC LEME (2005), CRC LEME 314-117
46. Uchiyama M., and Mihara M. Determination of malonaldehyde precursor in tissues by thiobarbituric acid test. Anal. Biochem. 86 (1978) 271-278
47. + when the Griess reaction is used to assay for nitrite. Anal. Biochem. 224 2 (1995) 502-508
48. Viarengo A., Burlando B., Cavaletto M., Marchi B., Ponzano E., and Blasco J. Role of metallothionein agaist oxidative stress in the mussel Mytilus galloprovincialis. Am. J. Physiol. Regul. Integr. Comp. Physiol. 277 (1999) 1612-1619