Differential effects of paraquat on oxidative stress parameters and polyamine levels in two freshwater invertebrates

Ecotoxicology and Environmental Safety

Volumn 68, Issue 2, 2007, Pages 286-292

  Cochon A C ^a   Della Penna, A B ^a   Kristoff, G ^a   Piol, M N ^a   San Martin de Viale L C ^a   Verrengia Guerrero, N R ^a  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

Biomphalaria glabrata; Catalase; Lipid peroxidation; Lumbriculus variegatus; Paraquat; Polyamines; Superoxide dismutase

Indexed keywords

CATALASE; LIPID; PARAQUAT; POLYAMINE; PUTRESCINE; SPERMIDINE; SPERMINE; SUPEROXIDE DISMUTASE;

CATABOLISM; ENZYME ACTIVITY; FRESHWATER ECOSYSTEM; GASTROPOD; HERBICIDE; ORGANIC COMPOUND; OXIDATION; PHOTOSYNTHESIS; POLLUTION EFFECT; SNAIL; TOXICITY;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ANNELID WORM; ARTICLE; BIOMPHALARIA GLABRATA; CONTROLLED STUDY; ENZYME ACTIVITY; FRESHWATER SPECIES; GASTROPOD; INVERTEBRATE; LIPID PEROXIDATION; NONHUMAN; OXIDATIVE STRESS;

ANIMALS; BIOMPHALARIA; CATALASE; FRESH WATER; HERBICIDES; LIPID PEROXIDATION; OLIGOCHAETA; OXIDATIVE STRESS; PARAQUAT; POLYAMINES; PUTRESCINE; SPERMIDINE; SPERMINE; SUPEROXIDE DISMUTASE; TIME FACTORS;

ANIMALIA; BIOMPHALARIA GLABRATA; GASTROPODA; INVERTEBRATA; LUMBRICULUS VARIEGATUS;

EID: 34548728548     PISSN: 01476513     EISSN: 10902414     Source Type: Journal    
DOI: 10.1016/j.ecoenv.2006.11.010     Document Type: Article

References (46)

1. Ali S., Diwakar G., and Pawa S. Paraquat induces different pulmonary biochemical responses in Wistar rats and Swiss mice. Chem. Biol. Interact. 125 (2000) 79-91
2. Bacchetta R., Mantecca P., and Vailati G. Oocyte degeneration and altered ovipository activity induced by paraquat in the freshwater snail Physa fontinalis (Gastropoda: Pulmonata). J. Molluscan Stud. 68 (2002) 181-186
3. Bayoumi A.E., Perez-Pertejo Y., Ordóñez C., Reguera R.M., Cubría J.C., Balaña-Fouce R., and Ordóñez D. Alterations on polyamine content and glutathione metabolism induced by different concentrations of paraquat in CHO-K1 cells. Toxicol. In vitro 14 (2000) 211-217
4. Cappelletti C., Maggioni M.G., and Maci R. Apoptosis in human lung epithelial cells triggered by paraquat and modulation by antioxidants. Cell Biol. Int. 22 (1998) 671-678
5. Cheng W.-H., Quimby F.W., and Lei X.G. Impacts of glutathione peroxidase-1 knockout on the protection by injected selenium against the pro-oxidant induced liver aponecrosis and signaling in selenium deficient mice. Free Rad. Biol. Med. 34 (2003) 918-927
6. Claiborne A. Catalase activity. In: Greenwald R. (Ed). CRC Handbook of Methods for Oxygen Radical Research (1985), CRC Press, Boca Raton, FL 283-284
7. Cochón A.C., González N., and San Martín de Viale L.C. Effects of the porphyrinogenic compounds hexachlorobenzene and 3,5 diethoxycarbonyl-1,4-dihydrocollidine on polyamine metabolism. Toxicology 176 (2002) 209-219
8. Dafre A.L., Dias Medeiros I., Müller I.C., Ventura E.C., and Dias Bainy A.C. Antioxidant enzymes and thiol/disulfide status in the digestive gland of the brown mussel Perna perna exposed to lead and paraquat. Chem. Biol. Interact. 149 (2004) 97-105
9. Das K.C., and Misra H.P. Hydroxyl radical scavenging and singlet oxygen quenching properties of polyamines. Mol. Cell Biochem. 262 (2004) 127-133
10. Dragin N., Smani M., Arnaud-Dabernat S., Dubost C., Moranvillier I., Costet P., Daniel J.-Y., and Peuchant E. Acute oxidative stress is associated with cell proliferation in the mouse liver. FEBS Lett. 580 (2006) 3845-3852
11. Drolet G., Dumbroff E.B., Legge R.L., and Thompson J.E. Radical scavenging properties of polyamines. Phytochemistry 25 (1986) 367-371
12. Eisler R. Paraquat hazard to fish, wildlife and invertebrates: A synoptic review. Contaminants Hazard Reviews. US Fish Wildlife Service Biol. Rep. 85 122 (1990)
13. Farbiszewski R., Bielawska A., Szymanska M., and Skrzydlewska E. Spermine partially normalizes in vivo antioxidant defense potential in certain brain regions in transiently hypoperfused rat brain. Neurochem. Res. 21 (1996) 1497-1503
14. Farriol M., Segovia-Silvestre T., Venero Y., and Orta X. Antioxidant effect of polyamines on erythrocyte cell membrane lipoperoxidation after free-radical damage. Phytother. Res. 17 (2003) 44-47
15. Figueiredo-Fernandes A., Fontaínhas-Fernandes A., Peixoto F., Rocha E., and Reis-Henriques M.A. Effects of gender and temperature on oxidative stress enzymes in Nile tilapia Oreochromis niloticus exposed to paraquat. Pest. Biochem. Physiol. 85 (2006) 97-103
16. Fried B., Sundar Rao K., and Sherma J. Fatty acid composition of Biomphalaria glabrata (Gastropoda: Planorbidae) fed hens′s egg yolk vs. leaf lettuce. Comp. Biochem. Physiol. 101A (1992) 351-352
17. Ha H.C., Sirisoma N.S., Kuppusamy P., Zweier J.L., Woster P.M., and Casero Jr. R.A. The natural polyamine spermine functions directly as a free radical scavenger. Proc. Natl. Acad. Sci. USA 95 (1998) 11140-11145
18. Haddad J.J. Redox and oxidant-mediated regulation of apoptosis signaling pathways: immuno-pharmaco-redox conception of oxidative siege versus cell death commitment. Int. Immunopharmacol. 4 (2004) 475-493
19. Hamana K., Hamana H., and Shinozawa T. Alterations in polyamine levels of nematode, earthworm, leech and planarian during regeneration, temperature and osmotic stresses. Comp. Biochem. Physiol. B 111 (1995) 91-97
20. Hegardt C., Andersson G., and Oredsson S.M. Spermine prevents cytochrome c release in glucocorticoid-induced apoptosis in mouse thymocytes. Cell Biol. Int. 27 (2003) 115-121
21. Hernández S.M., Sánchez M.S., and Schwarcz de Tarlovsky M.N. Polyamines as a defense mechanism against lipoperoxidation in Trypanosoma cruzi. Acta Trop. 98 (2006) 94-102
22. Hughes A., Smith N.I., and Wallace H.M. Polyamines reverse non-steroidal anti-inflammatory drug-induced toxicity in human colorectal cancer cells. Biochem. J. 374 (2003) 481-488
23. Kitada M., Igarashi K., Hirose S., and Kitagawa H. Inhibition by polyamines of lipid peroxide formation in rat liver microsomes. Biochem. Biophys. Res. Commun. 87 (1979) 388-394
24. Kurepa J., Smalle J., Van Montagu M., and Inze D. Polyamines and paraquat toxicity in Arabidopsis thaliana. Plant Cell Physiol. 39 (1998) 987-992
25. Lowry O.H., Rosebrough A., Farr L., and Randall R.S. Protein measurement with the folin phenol reagent. J. Biol. Chem. 249 (1951) 265-275
26. Misra H.P., and Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J. Biol. Chem. 247 (1972) 3170-3175
27. Nilsson J., Gritli-Linde A., and Heby O. Skin fibroblasts from spermine synthase-deficient hemizygous gyro male (Gy/Y) mice overproduce spermidine and exhibit increased resistance to oxidative stress but decreased resistance to UV irradiation. Biochem. J. 352 (2000) 381-387
28. Ohmori S., Misaizu T., Kitada M., Kitagawa H., Igarashi K., Hirose S., and Kanakubo Y. Polyamine lowered the hepatic lipid peroxide in rats. Res. Commun. Chem. Pathol. Pharmacol. 62 (1988) 235-249
29. Pedrajas J.R., Peinado J., and López-Barea J. Oxidative stress in fish exposed to model xenobiotics. Oxidatively modified forms of Cu,Zn-superoxide dismutase as potential biomarkers. Chem. Biol. Interact. 98 (1995) 267-282
30. Pegg A.E. Polyamine metabolism and its importance in neoplastic growth and a target for chemotherapy. Cancer Res. 48 (1988) 759-774
31. Rácz I., Lásztity D., Darkó E., Hidvégi E., and Szigeti Z. Paraquat resistance of horseweed (Erigeron canadensis L.) is not caused by polyamines. Pesticide Biochem. Physiol. 68 (2000) 1-10
32. Romero-Calderon R., and Krantz D.E. Transport of polyamines in Drosophila S2 cells: kinetics, pharmacology and dependence on the plasma membrane proton gradient. Biochem. J. 393 (2006) 583-589
33. Schipper R.G., Penning L.C., and Verhofstad A.A.J. Involvement of polyamines in apoptosis. Facts and controversies: effectors or protectors?. Semin. Cancer Biol. 10 (2000) 55-68
34. Sokal R.R., and Rohlf F.J. Biometry. The Principles and Practice of Statistic in Biological Research (1997), WH Freeman and Company, NY, USA
35. Suntres Z.E. Role of antioxidants in paraquat toxicity. Toxicology 180 (2002) 65-77
36. Tabor C.W., and Tabor H. Polyamines. Ann. Rev. Biochem. 53 (1984) 749-790
37. Tadolini B., Cabrini L., Landi L., Varani E., and Pasquali P. Polyamine binding to phospholipid vesicles and inhibition of lipid peroxidation. Biochem. Biophys. Res. Commun. 122 (1984) 550-555
38. Timbrell J.A. Introduction to Toxicology (1996), Taylor and Francis, London
39. Timbrell J.A. Principles of Biochemical Toxicology (2000), Taylor and Francis, London
40. Velloso Bellé N.A., Duarte Dalmolin G., Fonini G., Antonello Rubin M., and Teixeira Rocha J.B. Polyamines reduces lipid peroxidation induced by different pro-oxidant agents. Brain Res. 1008 (2004) 245-251
41. Verrengia Guerrero N.R., Taylor M.G., Davies N.A., Lawrence M.A.M., Edwards P.A., Simkiss K., and Wider E.A. Evidence of differences in the biotransformation of organic contaminants in three species of freshwater invertebrates. Environ. Pollut. 117 (2002) 523-530
42. Watanabe S., Sato S., Nagase S., Tomita M., and Saito T. Change of polyamine level in various tissues of male rats intoxicated with paraquat. Toxicol. Lett. 69 (1993) 163-170
43. Wenning R.J., Di Giulio R.T., and Gallagher E.P. Oxidant-mediated biochemical effects of paraquat in the ribbed mussel, Geukensia demissa. Aqua. Toxicol. 12 (1988) 157-170
44. Wesseling C., van Wendel de Joode B., Ruepert C., Leon C., Monge P., Hermosillo H., and Partanen T.J. Paraquat in developing countries. Int. J. Occup. Environ. Health 7 (2001) 275-286
45. Wiegand C., Pehkonen S., Akkanen J., Penttinen O.-P., and Kukkonen J.V.K. Bioaccumulation of paraquat by Lumbriculus variegatus in the presence of dissolved natural organic matter and impact on energy costs, biotransformation and antioxidative enzymes. Chemosphere 66 (2007) 558-566
46. Wills E.D. Evaluation of lipid peroxidation in lipids and biological membranes. In: Snell K., and Mullock B. (Eds). Biochemical Toxicology. A Practical Approach (1987), IRL Press, Oxford-Washington DC 127-152