Dose-dependent effects of ethanol on lead-induced oxidative stress in rats

Journal of Environmental Pathology, Toxicology and Oncology

Volumn 31, Issue 1, 2012, Pages 61-73

  Flora, S J S ^a   Gautam, Pratibha ^a   Dwivedi, Nidhi ^a  

^a DEFENCE RESEARCH AND DEVELOPMENT ESTABLISHMENT   (India)

Author keywords

Ethanol; Interaction; Lead; Oxidative stress

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ALCOHOL; ALCOHOL DEHYDROGENASE; ALDEHYDE DEHYDROGENASE; CALCIUM; CATALASE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUTATHIONE; GLUTATHIONE DISULFIDE; GLUTATHIONE PEROXIDASE; HEMOGLOBIN; LEAD; PORPHOBILINOGEN SYNTHASE; REACTIVE OXYGEN METABOLITE; THIOBARBITURIC ACID REACTIVE SUBSTANCE;

ALCOHOL INTOXICATION; ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; ARTICLE; CALCIUM CELL LEVEL; CONTROLLED STUDY; DECAPITATION; DOSE RESPONSE; ERYTHROCYTE; HEMATOCRIT; KIDNEY; LEAD POISONING; LEUKOCYTE; LIPID PEROXIDATION; LIVER; MALE; MEAN CORPUSCULAR HEMOGLOBIN; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; RAT;

ANIMALIA; RATTUS;

EID: 84861845999     PISSN: 07318898     EISSN: None     Source Type: Journal    
DOI: 10.1615/JEnvironPatholToxicolOncol.v31.i1.70     Document Type: Article

References (62)

1. Adonaylo VN, Oteiza PI. Lead intoxication: antioxidant defenses and oxidative damage in rat brain. Toxicology. 1999;135:77-85.
2. Albano E. Alcohol, oxidative stress and free radical damage. Proc Nutr Soci. 2006;65:278-290.
3. Pande M, Flora SJS. Lead induced oxidative damage and its response to combined administration of α-lipoic acid and DMSA in rats. Toxicology. 2002;177:187-196.
4. 2+ mobilization and increases GFAP content in rat hippocampal astrocytes. Brain Res. 2007;1178:28-37.
5. Farmand F, Ehdaie A, Roberts CK, Sindhu RK. Lead-induced dysregulation of superoxide dismutase, catalase, glutathione peroxidase, and guanylate cyclase. Environ Res. 2005;98:33-39.
6. Tran TD, Jackson HD, Horn KH, Goodlett CR. Vitamin E does not protect against neonatal ethanolinduced cerebellar damage or deficits in eyeblink classical conditioning in rats. Alcohol Clin Exp Res. 2005;29:117-129.
7. Costa CA, Trivelato GC, Pinto AMP, Bechara EJH. Correlation between plasma 5-aminolevulinic acid concentrations and indicators of oxidative stress in lead-exposed workers. Clin Chem. 1997;43:1196-1102.
8. Gurer-Orhan H, Sabir HU, Ozgunes H. Correlation between clinical indicator of lead poisoning and oxidative stress parameters in controls and lead exposed workers. Toxicology. 2004;195:147-154.
9. Kasperczyk S, Birkner E, Kasperczyk A, Kasperczyk J. Lipid, lipid peroxidation and 7-ketocholesterol in workers exposed to lead. Human Exp Toxicol. 2005;24:287-295.
10. Grandjean P. International perspectives of lead exposure and lead toxicity. Neurotoxicology. 1993;14:9-14.
11. Dey A, Cederbaum AI. Alcohol and oxidative liver injury. Hepatology. 2006;43:63-74.
12. Loguercio C, Piscopo P, Guerriero C, De Girolamo V, Disalvo D, Del Vecchio Blanco C. Effect of alcohol abuse and glutathione administration on the circulating levels of glutathione and on antipyrine metabolism in patients with alcoholic liver cirrhosis. Scand J Clin Lab Invest. 1996;56:441-447.
13. Ostrowska J, Luczaj W, Kasacka I, Rozanski A, Skrzydlewska E. Green tea protects against ethanol- induced lipid peroxidation in rat organs. Alcohol. 2004;32:25-32.
14. Fernandez-Checa JC, Kaplowitz N. Hepatic mitochondrial glutathione: transport and role in disease and toxicity. Toxicol App Pharm. 2005;204:263-273.
15. Bortoli A, Mattiello G, Fazzin G, Trabuio G F, Zotti S. Blood lead levels and ALA-D activity in exposed workers and in patients with alcoholic liver disease. Toxicol Lett. 1980;1:209-215
16. Cezard C, Demarquilly C, Boniface M, Haguenoern JM. Influence of the degree of exposure on lead on relations between alcohol consumption and the biological indices of lead exposure: epidemiological study in a lead acid battery factory. Br J Ind Med. 1992;49:645-647.
17. Flora SJS, Tandon SK. Effect of combined exposure to lead and ethanol on some biochemical indices in the rat. Biochem Pharmacol. 1987;36:537-541.
18. Flora SJ, Gautam P, Kushwah P. Lead and ethanol co-exposure lead to blood oxidative stress and subsequent neuronal apoptosis in rats. Alcohol Alcohol 2011 47:91-101.
19. Dhawan M, Flora SJS, Tandon SK. Biochemical changes and essential metals concentration in lead intoxicated rats pre-exposed to ethanol. Alcohol. 1992;9:241-245.
20. Berlin A, Schaller KH. European standardized method for the determination of delta aminolevulinic acid dehydratase activity in blood. Zeit Klin Chem Klin Biochem. 1974;12:389-390.
21. Ellman GL. Tissue sulfhydryl groups. Arch Biochem. 1959;82:70-77.
22. Jollow DJ, Mitchell JR, Zamppaglione Z, Gillette JR. Bromobenzene induced liver necrosis. Protective role of glutathione and evidence for 3, 4-bromobenzene oxide as the hepatotoxic metabolites. Pharmacology. 1974;11:151.
23. Socci DJ, Bjugstad KB, Jones HC, Pattisapu JV, Arendash GW. Evidence that oxidative stress is associated with the pathophysiology of inherited hydrocephalus in the H-Tx rat model. Exp Neurol. 1999;155:109-117.
24. Hissin PJ, Hilf R. A fluorometric method for the determination of oxidized and reduced glutathione in tissue. Anal Biochem. 1973;74:214-226.
25. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351-358.
26. Flohe L, Gunzler WA. Assays of glutathione peroxidase. Methods Enzymol. 1984;105:114-121.
27. Seth PK, Tangari KK. Biochemical effects of some newer salicylic acid congeners. J Pharm Pharmacol. 1966;18:831-833.
28. Fiske CH, Subbarow Y. The colorimeteric determination of phosphates. J Biol Chem. 1925;66:375-379.
29. Meder W, Fink K, Gothert M. Involvement of different calcium channels in K+ and veratidine-induced increase of cytoplasmic calcium concentration in rat cerebral cortical synaptosomes. Naunyn Scmedeberg Arch Pharmacol. 1997;356:797-805.
30. Ornstein L. Disc electrophoresis: background and theory. Ann N Y Acad Sci. 1964;121:321-403.
31. Scholl A, Anders S. Electrophoretic variation of enzyme proteins in Platyfish and Swordtails (Poeciliidae, Teleostei). Archiv Fur Genetik. 1973;46:121-129.
32. 2+. J Pharma Exp Therap. 2007;322:108-116.
33. Das SK, Vasudevan DM. Alcohol-induced oxidative stress. Life Sci. 2007;81:177-187.
34. Bechara EJH. Oxidative stress in acute intermittent porphyria and lead poisoning may be triggered by δ-aminolevulinic acid. Braz J Med Biol Res. 1996;29:841-851.
35. Ahamed M, Siddiqui MKJ. Low level lead exposure and oxidative stress: current opinions. Clin Chim Acta. 2007;383:57-64.
36. Yan M, Zhu P, Liu HM, Zhang HT, Liu L. Ethanol induced mitochondria injury and permeability transition pore opening: Role of mitochondria in alcoholic liver disease. World J Gastroenterol. 2007;13:2352-2356.
37. Jurczuk M, Jakoniuk JM, Brzoska MM. Involvement of some low-molecular thiols in the peroxidative mechanisms of lead and ethanol action on rat liver and kidney. Toxicology. 2006;219:11-21.
38. Trump BF, Berezesky IK. Calcium mediated cell injury and cell death. FASEB J 1995;9:219-228.
39. Turrens JF. Mitochondrial formation of reactive oxygen species. J Physiol. 2003;522:335-344.
40. Brookes PS, Yoon Y, Robotham JL, Anders MW, Sheu SS. Calcium, ATP, and ROS: a mitochondrial love-hate triangle. Am J Physiol Cell Physiol. 2004;287:817-833.
41. Bressler JP, Goldstein GW. Mechanisms of lead neurotoxicity. Biochem Pharmacol. 1991;41:479-484.
42. 2+-mediated ROS generation in mouse pancreatic acinar cells. Alcohol. 2006;38:51-57.
43. Balaban RS. Cardiac energy metabolism homeostasis: role of cytosolic calcium. J Mol Cell Cardiol. 2002;34:1259-1271.
44. Hansford RG, Zorov D. Role of mitochondrial calcium transport in the control of substrate oxidation. Mol Cell Biochem. 1998;184:359-369.
45. Teepker M, Anthes N, Fischer S, Krieg JC, Vedder H. Effects of oxidative challenge and calcium on ATP-levels in neuronal cells. Neurotoxicology. 2007;28:19-26.
46. 2+. Neurochem Res. 2003;28:1201-1211.
47. Mattson MP, Scheff SW. Endogenous neuroprotection factors and traumatic brain injury: mechanism of action and implications for therapy. J Neurotrauma. 1994;11:3-33.
48. Kristian T, Seisjo BK. Calcium related damage in ischemia. Life Sci. 1996;59:357-367.
49. Coyle JT, Puttfarcken P. Oxidative stress, glutamate and neurodegenerative disorders. Science. 1993;262:689-695.
50. Hsu PC, Guo YL. Antioxidant nutrients and lead toxicity. Toxicology. 2002;180:33-44.
51. Hsu JM. Lead toxicity related to glutathione metabolism. J Nutr. 1981;111:26-33.
52. Ito Y, Niiya Y, Kurita H, Shima S, Sarai S. Serum lipid peroxide level and blood superoxide dismutase activity in workers with occupational exposure to lead. Int Arch Occup Environ Health. 1985;56:119-127.
53. McGowan C, Donaldson WE. Changes in organ nonprotein sulfhydryl and glutathione concentrations during acute and chronic administration of inorganic lead to chicks. Biol Trace Elem Res. 1986;10:37-46.
54. Chiba M, Shinohara A, Matsushita K, Watanabe H, Inaba Y. Indices of lead-exposure in blood and urine of lead-exposed workers and concentrations of major and trace elements and activities of SOD, GSH-Px and catalase in their blood. Tohoku J Exp Med. 1996;178:49-62.
55. Lachant NA, Tomoda A, Tanaka KR. Inhibition of the pentose phosphate shunt by lead: a potential mechanism for hemolysis in lead poisoning. Blood. 1984;63:518-524.
56. Gurer H, Ozgunes H, Neal R, Spitz DR, Ercal N. Antioxidant effects of N-acetylcysteine and succimer in red blood cells from lead-exposed rats. Toxicology. 1998;128:181-189.
57. Cocco P, Salis S, Anni M, Coccco ME, Flore C, Ibba A. Effects of short-term occupational exposure to lead on erythrocyte glucose-6-phosphate dehydrogenase activity and serum cholesterol. J Appl Toxicol. 1995;15:375-378.
58. Gurer H, Ercal N. Can antioxidants be beneficial in the treatment of lead poisoning. Free Radic Biol Med. 2000;29:927-945.
59. Gelman BB, Michaelson IA, Bus JS. The effect of lead on oxidative hemolysis and erythrocyte defense mechanisms in the rat. Toxicol Appl Pharmacol. 1978;45:119-129.
60. Signorini-Allibe N, Gonthier B, Lamarche F, Eysseric H, Barret L. Chronic consumption of ethanol leads to substantial cell damage in cultured rat astrocytes in conditions promoting acetaldehyde accumulation. Alcohol. 2005;40:163-171.
61. Zimatkin SM, Pronko SP, Vasiliou V, Gonzalez FJ, Deitrich RA. Enzymatic mechanisms of ethanol oxidation in the brain. Alcoholism. 2006;30:1500-1505.
62. Montoliu C, Sancho-Tello M, Azorin I, Burgal M, Valles S, Reanu-Piqueras J, Guerri C. Ethanol increases cytochrome P450 and induces oxidative stress in astrocytes. J Neurochem. 1995;65:2561-2570.