Oxidative stress induced by lambda-cyhalothrin (LTC) in rat erythrocytes and brain: Attenuation by vitamin C

Environmental Toxicology and Pharmacology

Volumn 26, Issue 2, 2008, Pages 225-231

  Fetoui, Hamadi ^a   Garoui, El Mouldi ^a   Makni ayadi, Fatma ^b   Zeghal, Najiba ^a  

^a Faculté des Sciences de Sfax   (Tunisia)

^b HABIB BOURGUIBA HOSPITAL   (Tunisia)

Author keywords

Brain; Erythrocytes; Lambda cyhalothrin; Oxidative damage; Pyrethroid insecticide; Rat; Vitamin C

Indexed keywords

ASCORBIC ACID; CATALASE; CYHALOTHRIN; GLUTATHIONE; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; GLUTATHIONE TRANSFERASE; HEMOGLOBIN; INSECTICIDE; LACTATE DEHYDROGENASE; MALONALDEHYDE; PYRETHROID; SUPEROXIDE DISMUTASE;

ANEMIA; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; BRAIN; CONTROLLED STUDY; ENZYME ACTIVITY; ERYTHROCYTE; FLUID INTAKE; FOOD INTAKE; HEMATOCRIT; HEMATOLOGICAL PARAMETERS; HEMOGLOBIN DETERMINATION; LIPID PEROXIDATION; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN CONTENT; RAT; SINGLE DRUG DOSE; TISSUE DISTRIBUTION;

ANIMALIA; RATTUS; RATTUS NORVEGICUS;

EID: 47849100731     PISSN: 13826689     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.etap.2008.04.002     Document Type: Article

References (63)

1. Adhikari S., Sarkar B., Chatterjee A., Mahapatra C.T., and Ayyappan S. Effects of cypermethrin and carbofuran on certain haematological parameters and prediction of their recovery in a freshwater teleost, Labeo rohita (Hamilton) Ecotoxicol. Environ. Saf. 58 (2004) 220-226
2. Aebi H. Catalase in vitro. Method Enzymol. 105 (1984) 121-126
3. Antunes-Madeira M.C., Videira R.A., and Madeira V.M.C. Effects of parathion on membrane organization and its implications for the mechanisms of toxicity. Biochem. Biophys. Acta 1190 (1994) 149-154
4. Appenroth D., Frög S., Kersten L., and Splinter F.K. Protective effects of vitamin E and C on Cisplatin nephrotoxicity in developing rats. Arch. Toxicol. 71 (1997) 677-683
5. Awumbila B., and Bokuma E. Survey of pesticides used in the control of ectoparasites on farm animals in Ghana. Trop. Anim. Health Prod. 26 (1994) 7-12
6. Bergmeyer H.U., Bernt E., and Beneno H. Lactate dehydrogenase. In: Bergmeyer H.U. (Ed). Methods of Enzymatic Analysis vol. 2 (1974), Verlag Chemie Weinheim, Academic Press, Inc., New York and London 736-738
7. Campana M.A., Panzeri A.M., Moreno V.J., and Dulout F.N. Genotoxic evaluation of the prethroid lambda-cyhalothrin using the micronucleus test in erythrocytes of fish Cheirodon interruptus. Mutat. Res. 438 (1999) 155-161
8. Carlberg I., and Mannervik B. Glutathione reductase levels in rat brain. J. Biol. Chem. 250 (1975) 5475-5480
9. Casida J.E., and Quistad G.B. Golden age of insecticide research: past, present, or future? Annu. Rev. Entomol. 43 (1998) 1-16
10. Çelik A., Mazmanci B., Çamlica Y., Askin A., and çömelekoglu U. Cytogenitic effects of lambda-cyhalothrin on wistar rat bone marrow. Mutat. Res. 539 (2003) 91-97
11. Çelik A., Mazmanci B., Çamlica Y., çömelekoglu U., and Askin A. Evaluation of cytogenetic effects of lambda-cyhalothrin on Wistar rat bone marrow by gavage administration. Ecotoxicol. Environ. Saf. 61 (2005) 128-133
12. Clemens R., and Waller H.D. Lipid peroxidation in erythrocytes. Chem. Phys. Lipids 45 (1987) 251-268
13. Ellman G.L. Tissue sulfhydryl groups. Arch. Biochem. 82 (1959) 70-77
14. Erstfeld K.M. Environmental fate of synthetic pyrethroids during spary drift and field runoff treatments in aquatic microcosms. Chemosphere 39 (1999) 1737-1769
15. Evans P.H. Free radicals in brain metabolism and pathology. Br. Med. Bull. 49 (1993) 577-587
16. Evans P., and Halliwell B. Micronutrients: oxidant/antioxidant status. Br. J. Nutr. 85 (2001) S67-S74
17. Fahmy A.M., and Abdallah E.F. Cytogenetic effects by the natural pyrethrins and the synthetic lambda-cyhalothrin in mice in vivo. Cytologia 66 (2001) 139-149
18. Fetoui H., Mahjoubi-Samet A., Jammousi K., Ellouze F., Guermazi F., and Zeghal N. Energy restriction in pregnant and lactating rats lowers bone mass of their progeny. Nutr. Res. 26 (2006) 421-426
19. Fetoui H., Mahjoubi-Samet A., Jamoussi K., Ayadi F., Ellouze F., and Zeghal N. Food restriction in pregnant and lactating rats induces anemia and increases plasma lipid peroxidation in their progeny. Nutr. Res. 27 (2007) 788-793
20. Flohe L., and Gunzler W.A. Assays of glutathione peroxidase. Method Enzymol. 105 (1984) 114-121
21. French J.K., Winterbourn C.C., and Carrel R.W. Mechanism of oxyhaemoglobin breakdown on reaction with acetyl phenyl hydrazine. Biochem. J. 173 (1978) 19-26
22. Gabbianelli R., Falcioni G., Nasuti C., and Cantalamessa F. Cypermethrin-induced plasma membrane perturbation on erythrocytes from rats: reduction of fluidity in the hydrophobic core and in glutathione peroxidase activity. Toxicology 175 (2002) 91-101
23. Giray B., Gurbay A., and Hincal F. Cypermethrin-induced oxidative stress in rat brain and liver is prevented by vitamin E and allopurinol. Toxicol. Lett. 118 (2001) 139-146
24. Gokalpa O., Buyukvanli{dotless} B., Cicek E., Ozer M.K., Koyu A., Altuntas I., and Koylu H. The effects of diazinon on pancreatic damage and ameliorating role of vitamin E and vitamin C. Pest Biochem. Phys. 81 (2005) 123-128
25. Grajeda-Cota P., Ramirez-Mares M.V., and Mejia E.G. Vitamin C protects against in vitro cytotoxicity of cypermethrin in rat hepatocytes. Toxicol. in vitro 18 (2004) 13-19
26. Habig W.H., Pabst M.J., and Jokoby W.B. Glutathione-S-transferase: the first enzymatic step in mercapturic acid formation. J. Biol. Chem. 249 (1974) 7130-7139
27. Hunter F.E., Gebicki J.M., HoVsten P.E., Weinstein J., and Scott A. Swelling and lysis of rat liver mitochondria induced by ferrous irons. J. Biol. Chem. 238 (1963) 828-835
28. Jollow D.J., Mitchell J.R., Zamppaglione Z., and Gillette J.R. Bromobenzene induced liver necrosis. Protective role of glutathione and evidence for 3, 4-bromobenzene oxide as the hepatotoxic metabolites. Pharmacology 11 (1974) 51-157
29. ++-ATPase. Pestic Biochem. Physiol. 25 (1986) 420-430
30. Kale M., Rathore N., John S., and Bhatnagar D. Lipid peroxidative damage on pyrethroid exposure and alterations in antioxidant status in rat erythrocyte: a possible involvement of reactive oxygen species. Toxicol. Lett. 105 (1999) 197-205
31. Kanbur, M., Liman, B.C., Eraslan, G., Altinordulu, S., 2008. Effects of cypermethrin, propetamphos, and combination involving cypermethrin and propetamphos on lipid peroxidation in mice Environ. Toxicol., in press.
32. Kato G.J., McGowan V., Machado R.F., Little J.A., Taylor J., Morris C.R., James S., Wang N.X., Poljakovic M., Morris S.M., and Gladwin M.T. Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease. Blood 107 (2006) 2279-2285
33. Kilian E., Delport R., Bornman M.S., and de Jager C. Simultaneous exposure to low concentrations of dichlorodiphenyltrichloroethane, deltamethrin, nonylphenol and phytoestrogens has negative effects on the reproductive parameters in male Sprague-Dawley rats. Andrologia 39 (2007) 128-135
34. Kono Y., and Fridovich I. Superoxide inhibits catalase. J. Biol. Chem. 257 (1992) 5751-5754
35. Lowry O.H., Rosebrough N.J., Farr A.L., and Randall R.J. Protein measurement with folin phenol reagent. J. Biol. Chem. 193 (1951) 265-270
36. Manna S., Battacharyya D., Mandal T.K., and Das S. Repeated dose toxicity of alfa-cypermethrin in rats. J. Vet. Sci. 5 (2004) 241-245
37. Marklund S., and Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur. J. Biochem. 47 (1974) 469-474
38. Michelangeli F., Robson M.J., East J.M., and Lee A.G. The conformation of pyrethroids bound to lipid bilayers. Biochem. Biophys. Acta 1028 (1990) 49-57
39. Mishra R., and Shukla S.P. Endosulfan effects on muscle malate dehydogenase of the freshwater catfish Clarias batrachus. Ecotoxicol. Environ. Saf. 56 (2003) 425-433
40. Mohandas J., Marshall J.J., Duggin G.G., Horvath J.S., and Tiller D. Differential distribution of glutathione and glutathione related enzymes in rabbit kidneys. Possible implication in analgesic neuropathy. Cancer. Res. 44 (1984) 5086-5091
41. Narahashi T. Nerve membrane ionic channels as the primary target of pyrethroids. Neurotoxicology 6 (1985) 3-22
42. Nasuti C., Cantalamessa F., Falcioni G., and Gabbianelli R. Different effects of type I and type II pyrethroids on erythrocyte plasma membrane properties and enzymatic activity in rats. Toxicology 191 (2003) 233-244
43. Parker C.M., Piccirillo V.J., Kurtz S.L., Garner F.M., Gardiner T.H., and Van Gelder G.A. Six-month feeding study of fenvalerate in dogs. Fundam. Appl. Toxicol. 4 (1984) 577-586
44. Patel S., Singh V., Kumar A., Gupta Y.K., and Singh M.P. Status of antioxidant defense system and expression of toxicant responsive genes in striatum of maneb- and paraquat-induced Parkinson's disease phenotype in mouse: mechanism of neurodegeneration. Brain Res. 1081 (2006) 9-18
45. Perez-Albarsanz M.A., Lopez-Aparicio P., Senar S., and Reco M.N. Effects of lindane on fluidity and lipid composition in rat renal cortex membranes. Biochem. Biophys. Acta 1066 (1991) 124-130
46. Prasanthi K., Muralidhara R., and Rajini P.S. Fenvalerate-induced oxidative damage in rat tissues and its attenuation by dietary sesame oil. Food Chem. Toxicol. 43 (2005) 299-306
47. Ray D.E., and Fry J.R. Reassessment of the neurotoxicity of pyrethroid insecticides. Pharmacol. Ther. 111 (2006) 174-193
48. Sae-Yong H., Kyu-Yoo H., Eun-Young L., Soo-Whon E., Suk-Ran C., Chan-Soo H., Yung-Hyun P., and Sung-Keun C. Effect of vitamin C on plasma total antioxidant status in patients with paraquat intoxication. Toxicol. Lett. 126 (2002) 51-59
49. Samson F.E., and Nelson S.R. The aging brain, metals and oxygen free radicals. Cell. Mol. Biol. 46 (2000) 699-707
50. Sarkar S.N., Balasubramanian S.V., and Sikdar S.K. Effect of Fenvalerate, a pyrethroid insecticide on membrane fluidity. Biochem. Biophys. Acta 1147 (1993) 137-142
51. Schenone H., and Rojas A. Laboratory study on the immediate and persistent insecticide activity of the pyrethroid lambda-cyhalothrin on nymphs of IV instar Triatoma infestans. Bol. Chil. Parasitol. 47 (1992) 35-37
52. 2. Arch. Biochem. Biophys. 212 (1981) 411-416
53. Sinha C., Seth K., Islam F., Kumar R., Shukla C.S., Mathur N., and Srivastava Agrawal K. Behavioral and neurochemical effects induced by pyrethroid-based mosquito repellent exposure in rat offsprings during prenatal and early postnatal period. Neurotoxicol. Teratol. 28 (2006) 472-481
54. Sinha M., Manna P., and Sil P.C. A 43 kD protein from the herb, Cajanus indicus L., protects against fluoride induced oxidative stress in mice erythrocytes. Pathophysiology 14 (2007) 47-54
55. Soderlund D.M., Clark J.M., Sheets L.P., Mullin L.S., Piccirillo V.J., Sargent D., Stevens J.T., and Weiner M.L. Mechanisms of pyrethroid neurotoxicity: implications for cumulative risk assessment. Toxicology 171 (2002) 3-59
56. Srivastava A., and Shivanandappa T. Hexachlorocyclohexane differentially alters the antioxidant status of the brain regions in rat. Toxicology 214 (2005) 123-130
57. Sulak O., Altuntas I., Karahan N., Yildirim B., Akturk O., Yilmaz H.R., and Delibas N. Nephrotoxicity in rats induced by organophosphate insecticide methidathion and ameliorating effects of vitamin E and C. Pestic. Biochem. Physiol. 83 (2005) 21-28
58. Svoboda M., Luskova V., Drastichova J., and Ilabek V. The effect of diazinon on hematological indices of common carp (Cyprinus carpio L.). Acta Vet. 70 (2001) 457-465
59. Tavares D.M., Martins M.L., and Nascimento K.S. Evaluation of the hematological parameters in Piaractus mesopotomicus Holmberg (Osteichthyes, Characidae) with Argulus sp. (Crustacea Branchiura) infestation and treatment with organophosphate. Rev. Bras. Zool. 16 (1999) 553-555
60. Tripathi G., and Shukla S.P. Malate and lactate dehydrogenases of a freshwater cat fish, impact of endosulfan. Biomed. Environ. Sci. 3 (1990) 52-58
61. Vijverberg H.P., and van den Bercken J. Neurotoxicological effects and the mode of action of pyrethroid insecticides. Crit. Rev. Toxicol. 21 (1990) 105-126
62. World Health Organisation (WHO). Cyhalothrin, Environmental Health Criteria (1990), International Program on Chemical Safety, Geneva
63. Yavuz T., Delibas N., Yildirm B., Altuntas I., Candir O., Cora A., Karahan, Ibrisim N., and Kustal E. Vascular wall damage in rats induced by methidathion and ameliorating effect of vitamin E and C. Hum. Exp. Toxicol. 78 (2004) 655-659