Oxidative stress in human erythrocytes treated with bromfenvinphos and its impurities

Pesticide Biochemistry and Physiology

Volumn 118, Issue , 2015, Pages 43-49

  Sosnowska, Bozena ^a,b   Huras, Bogumiła ^c   Bukowska, Bozena ^a  

^a UNIVERSITY OF LODZ   (Poland)

^b MEDICAL UNIVERSITY OF LODZ   (Poland)

^c INSTITUTE OF INDUSTRIAL ORGANIC CHEMISTRY   (Poland)

Author keywords

Antioxidant enzymes; Bromfenvinphos; Erythrocytes; Glutathione; Lipid peroxidation; Reactive oxygen species

Indexed keywords

BROMFENVINPHOS; CLOFENVINFOS; GLUTATHIONE; GLUTATHIONE PEROXIDASE; INSECTICIDE; SUPEROXIDE DISMUTASE;

ANALOGS AND DERIVATIVES; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECTS; ENZYMOLOGY; ERYTHROCYTE; HUMAN; METABOLISM; OXIDATIVE STRESS;

CHLORFENVINPHOS; ERYTHROCYTES; GLUTATHIONE; GLUTATHIONE PEROXIDASE; HUMANS; INSECTICIDES; MOLECULAR STRUCTURE; OXIDATIVE STRESS; SUPEROXIDE DISMUTASE;

EID: 84924022456     PISSN: 00483575     EISSN: 10959939     Source Type: Journal    
DOI: 10.1016/j.pestbp.2014.11.009     Document Type: Article

References (62)

1. Moszczyński W. Pesticide industry in Poland and cooperation ability with developing countries. Pesticides 1990, 1:157-180.
2. M. Bieńkowska, Drugs used to combat parasite Varroa destructor in the years 1996-2005, Mat. XXXIX Nauk. Science Conf., Puławy 24-25 April, (2007) 59-60.
3. D. Bombińska, L. Cieślak, B. Huras, J. Kazimierczak, Apifos - the first year of application, Mat. XVI Science Conf. Varroasis and apiary management, Olsztyn-Kortowo 15 May, (2000) 5-6.
4. Baker M.D., Peng C.Y.S. Varroa jabosconi and Tropilaelaps clareae: a perspective of life history and why Asian bee mites preferred European honeybee. Am. Bee J. 1995, 135:415-420.
5. Razowski J. List of Animals in Poland. T. 4 1997, 196. Publications of the Institute of Systematic and Evolution of Animals, Cracow.
6. Rosenkranz P., Aumeier P., Ziegelmann B. Biology and control of Varroa destructor. J. Invert. Pathol 2010, 103:96-119.
7. Fries I., Imdorf A., Rosenkranz P. Survival of mite infested (Varroa destructor) honey bee (Apis mellifera) colonies in a Nordic climate. Apidologie 2006, 37:564-570.
8. Neumann P., Carreck N. Honey bee colony losses. J. Apicult. Res 2010, 49:1-6.
9. Z. Konopacka, D. Gerula, The effectiveness of several formulation against Varroa destructor available in Poland, Mat. XXXVIII Science Conf., Puławy 13-14 March, (2001) 41-42.
10. Z. Konopacka, D. Gerula, M. Bieńkowska, The effectiveness of several formulation against Varroa destructor available in Poland in research Apiculture Division, Mat. XXXIX Science. Conf., Puławy 12-13 March, (2002) 56-57.
11. Prohecka K., Bober A. Resistance of Varroa destructor to the most commonly used acaricides. Med. Wet 2007, 63:904-908.
12. Directive 2004/28/EC of European Parliament and Council of 31 March 2004 amending Directive 2001/82/EC on the Community code relating to veterinary medicinal products.
13. Council Directive 91/414/EE, 15 July 1991, concerning the placing of plant protection products Official Journal L 230, 19/08/1991 P. 0001 0032.
14. Savolainen K. Understanding the Toxic Action of Organophosphates, W: Handbook of Pesticide Toxicology 2001, Academic Press, USA.
15. Costa L.G. Current issues in organophosphate toxicology. Clin. Chim. Acta 2006, 306:1-13.
16. Ranjbar A., Ghahremani M.H., Sharifzadeh M., Golestani A., Ghazi-Khansari M., Baeeri M., et al. Protection by pentoxifylline of malathion-induced toxic stress and mitochondrial damage in rat brain. Hum. Exp. Toxicol 2010, 29:851-864.
17. Franco J.L., Posser T., Mattos J.J., Trevisan R., Brocardo P.S., Rodrigues A.L., et al. Zinc reverses malathion-induced impairment in antioxidant defenses. Toxicol. Lett 2009, 187:137-143.
18. Sosnowska B., Huras B., Nowacka-Krukowska H., Bukowska B. Oxidative damage to human red blood cells treated with chlorfenvinphos, an organophosphate insecticide (in vitro). Biologia (Bratisl) 2013, 66:379-385.
19. Bayrami M., Hashemi T., Malekirad A.A., Ashayeri H., Faraji F., Abdollahi M. Electroencephalogram, cognitive state, psychological disorders, clinical symptom, and oxidative stress in horticulture farmers exposed to organophosphate pesticides. Toxicol. Ind. Health 2012, 28:90-96.
20. Lopez O., Hernandez A.F., Rodrigo L., Gil F., Pena G., Serrano J.L., et al. Changes in antioxidant enzymes in humans with long-term exposure to pesticides. Toxicol. Lett 2007, 171:146-153.
21. Ogut S., Gultekin F., Kisioglu A.N., Kucukoner E. Oxidative stress in the blood of farm workers following intensive pesticide exposure. Toxicol. Ind. Health 2011, 27:820-825.
22. Pandey K.B., Rizvi S.I. Biomarkers of oxidative stress in red blood cells. Biomed. Pap. Med. Fac. Univ. Palacky Olomouc Czech. Repub 2011, 155:131-136.
23. Bonarska-Kujawa D., Pruchnik H., Cyboran S., Zyłka R., Oszmiański J., Kleszczyńska H. Biophysical mechanism of the protective effect of blue honeysuckle (Lonicera caerulea L. Var. Kamtschatica Sevast.) polyphenols extracts against lipid peroxidation of erythrocyte and lipid membranes. J. Membr. Biol 2014, 247:611-625.
24. Krokosz A., Grebowski J., Szweda-Lewandowska Z., Rodacka A., Puchała M. Can melatonin delay oxidative damage of human erythrocytes during prolonged incubation?. Adv. Med. Sci 2013, 58:134-142.
25. Kwiatkowska M., Huras B., Bukowska B. The effect of metabolites and impurities of glyphosate on human erythrocytes (in vitro). Pestic. Biochem. Physiol 2014, 109:34-43.
26. Rowiński R., Kozakiewicz M., Kedziora-Kornatowska K., Hübner-Wozniak E., Kedziora J. Markers of oxidative stress and erythrocyte antioxidant enzyme activity in older men and women with differing physical activity. Exp. Gerontol 2013, 48:1141-1146.
27. Bartosz G. The Other Face of Oxygen. Free Radicals in Nature 2009, PWN, Warsaw.
28. Sosnowska B., Huras B., Krokosz A., Bukowska B. The effect of bromfenvinphos, its impurities and chlorfenvinphos on acetylocholinesterase activity. Int. J. Biol. Macromol 2013, 57:38-44.
29. Szatkowska B., Bukowska B., Huras B. The effect of bromfenvinphos and its impurities on human erythrocyte. Food Chem. Toxicol 2011, 49:502-507.
30. Felicia V.S., Guthrie N., Chambers A.F., Carroll K.K. Inhibition of proliferation of estrogen receptor-positive MCF-7 human breast cancer cells by flavonoids in the presence and absence of excess estrogen. Cancer Lett 1997, 112:127-133.
31. Drabkin D.L. Spectrophotometric studies. XIV. The crystallographic and optical properties of the hemoglobin of man in comparison with those of other species. J. Biol. Chem 1946, 164:703-723.
32. Bartosz G. Use of spectroscopic probes for detection of reactive oxygen species. Clin. Chim. Acta 2006, 368:53-76.
33. Stocks J., Dormandy T.L.J. The autooxidation of red cell lipids induced by hydrogen peroxide. B. J. Haematol 1971, 20:95-111.
34. Aebi H. Catalase in vitro. Met. Enzymol 1984, 105:121-126.
35. Misra H.P., Fridrovich I. The generation of superoxide radical during autooxidation of hemoglobin. J. Biol. Chem 1972, 47:6960-6962.
36. Ellman G. Tissue sulfhydryl groups. Arch. Biochem. Biophys 1959, 82:70-77.
37. H. Nowacka-Krukowska, W. Londzin, Bromfenvinphos and other synthetic acaricide as residues in bee products, Mat. XIV Science Conf. Varroasis and apiary management, Olsztyn-Kortowo, 11 May, (1998) 18-22.
38. Matysik-Pejas R. Conditioned honey consumption in households (selected regions of the province of Malopolska). Assoc. Agric. Agribus. Econ 2007, 9:125.
39. URL Eurostat accessed 14.03.09. http://epp.eurostat.ec.europa.eu.
40. Sosnowska B., Witaszewska J., Słowińska M., Michałowicz J., Huras B., Bukowska B. Hemolysis and methemoglobin formation in erythrocytes incubated with bromfenvinphos and its impurities. Monogr. Compr. Res. Protect. Environ. - Diagn. State Environ. Res. Methods Forecasts ARTKAMI Bydgoszcz 2012, VI:257-266.
41. Bratkowski J., Wilde J., Bak B. Sensitivity beeswax contamination remains after medication. Pasieka 2003, 3.
42. Wallner K. Varroacides and their residues in bee products. Apidologie 1999, 30:235-248.
43. Bogdanov S. Contaminants of bee products. Apidologie 2006, 37:1-18.
44. Kochansky J., Wilzer K., Feldlaufer M. Comparison of the transfer of coumaphos from beeswax into syrup and honey. Apidologie 2001, 32:119-125.
45. A.S. Dorsey, S.S. Kueberuwa, Department of Health and Human Services, Public Health Service, Agency for Toxic Substances and Disease Registry (1997) 1-220.
46. Kroczyński J., Malinowski H. Insecticidal characteristic of bromfenvinphos. Prog. Sci. Rol 1977, 24:85-96.
47. Łukasiewicz-Hussain A., Moniuszko-Jakoniuk J. Chlorfenvinphos, an organophosphate insecticide, affects liver mitochondria antioxidative enzymes, glutathione and hydrogen peroxide concentration. Pol. J. Environ. Stud 2004, 13:397-401.
48. Łukasiewicz-Hussain A., Moniuszko-Jakoniuk J. A low dose of chlorfenvinphos affects hepatic enzymes in serum and antioxidant enzymes in erythrocytes and liver of rats. Pol. J. Environ. Stud 2005, 14:199-202.
49. Łukasiewicz-Hussain A. Subchronic intoxication with chlorfenvinphos, an organophosphate insecticide, affects rat brain antioxidative enzymes and glutathione level. Food Chem. Toxicol 2008, 46:82-86.
50. Shadnia S., Azizi E., Hosseini R., Khoei S., Fouladdel S., Pajoumand A., et al. Evaluation of oxidative stress and genotoxicity in organophosphorus insecticide formulators. Hum. Exp. Toxicol 2005, 24:439-445.
51. Roszczenko A., Rogalska J., Joniuszko-Jakoniuk J., Brzóska M.M. The effect of exposure to chlorfenvinphos on lipid metabolism and apoptotic and necrotic cells death in the brain of rats. Exp. Toxicol. Pathol 2012, 65:531-539.
52. Łukasiewicz-Hussain A., Moniuszko-Jakoniuk J., Rogalska J. Assessment of lipid peroxidation in rat tissues in subacute chlorfenvinphos administration. Polish J. Environ. Stud 2007, 16:233-236.
53. Abdollahi M., Ranjbar A., Shadnia A., Nikfar S., Rezaie A. Pesticides and oxidative stress: a review. Med. Sci. Monit 2004, 10:141-147.
54. Baltazar M.T., Dinis-Oliveira R.J., De Lourdes Bastos M., Tsatsakis A.M., Duarte J.A., Carvalho F. Pesticides exposure as etiological factors of Parkinson's disease and other neurodegenerative diseases - a mechanistic approach. Toxicol. Lett 2014, 10.1016/j.toxlet.2014.01.039.
55. Doganay S., Duz C., Firat P.G., Cankaya C., Kutukde D., Cigremis Y. The effect of apricots on the experimental cataract model formed by sodium selenite. Food Chem. Toxicol 2013, 55:371-377.
56. Gubandru M., Margina D., Tsitsimpikou C., Goutzourelas N., Tsarouhas K., Ilie M., et al. Alzheimer's disease treated patients showed different patterns for oxidative stress and inflammation markers. Food Chem. Toxicol 2013, 61:209-214.
57. Schrag M., Mueller C., Zabel M., Crofton A., Kirsch W.M., Ghribi O., et al. Oxidative stress in blood in Alzheimer's disease and mild cognitive impairment: a meta-analysis. Neurobiol. Dis 2013, 59:100-110.
58. Szymańska J.A. Hepatotoxicity of brominated benzene: relationship between chemical structure and hepatoxic effects in acute intoxication of mice. Arch. Toxicol 1998, 72:97-103.
59. Bronowska K. Thermodynamics of ligand-protein interactions: implications for molecular design. Thermodynamics - Interaction Studies - Solids, Liquids and Gases: InTech 2011, 10.5772/19447. J.C. Moreno-Pirajan (Ed.).
60. Ścibior D., Czeczot H. Catalase - structure, properties, functions. Adv. Hyg. Exp. Med 2006, 60:170-180.
61. Bukowska B., Chajdys A., Duda W., Duchnowicz P. Catalase activity in human erythrocytes: effect of phenoxyherbicides and their metabolites. Cell Biol. Int 2000, 24:705-711.
62. Zheleva A., Gadjeva V., Zheleva M. Free radical formation might contribute to the severe amatoxin hepatotoxicity. Trakia J. Sci 2003, 1:42-45.