Co-exposure to arsenic and fluoride on oxidative stress, glutathione linked enzymes, biogenic amines and DNA damage in mouse brain

Journal of the Neurological Sciences

Volumn 285, Issue 1-2, 2009, Pages 198-205

  Flora, S J S ^a   Mittal, Megha ^a   Mishra, Deepshikha ^a  

^a DEFENCE RESEARCH AND DEVELOPMENT ESTABLISHMENT   (India)

Author keywords

Arsenic; Combined exposure; DNA damage; Fluoride; Mouse; Neurotoxicity; Oxidative stress; Spectroscopy

Indexed keywords

ACETYLCHOLINESTERASE; ALPHA TOCOPHEROL; AMINE OXIDASE (FLAVIN CONTAINING); ARSENIC; BIOGENIC AMINE; CATALASE; DNA; FLUORIDE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUTATHIONE; SUPEROXIDE DISMUTASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN; BRAIN METABOLISM; CONTROLLED STUDY; DNA DAMAGE; DNA STRUCTURE; ENZYME ACTIVITY; GENOTOXICITY; HEAVY METAL POISONING; MOUSE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL;

ANIMALS; ARSENITES; BIOGENIC AMINES; BRAIN; CENTRAL NERVOUS SYSTEM AGENTS; DNA; DNA DAMAGE; GLUTATHIONE; MALE; MICE; NUCLEIC ACID CONFORMATION; OXIDATIVE STRESS; RANDOM ALLOCATION; SODIUM COMPOUNDS; SODIUM FLUORIDE; VITAMIN E;

EID: 69549088025     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jns.2009.07.001     Document Type: Article

References (57)

1. NRC. Arsenic in drinking water (1999), National Research Council, National Academy Press, Washington, DC
2. Mullenix P.J., Denbesten P.K., Schunior A., and Kernan W.J. Neurotoxicity of sodium fluoride in rats. Neurotoxicol Teratol 17 (1995) 169-177
3. Trejo-Vazquez R., Bonilla-Petriciolet A., and Ortiz-Gomez A. Fluoride and arsenic concentrations in groundwater of Aguascalientes, Mexico. Rev Panam Salud Publica 4 (2001) 194
4. Sun G.F. The problem of arsenic pollution in water and endemic arsenic poisoning faced by China. Environ Health Perspect 113 (2005) 23-32
5. Jhala D.D., Nair S.B., and Chinoy N.J. Reversible toxicity of fluoride and arsenic in ovary of mice. Fluoride 37 (2004) 71-79
6. Bharath S., Hsu M., Kaur D., Rajagopalan S., and Andersen J.K. Glutathione, iron and Parkinson's disease. Biochem Pharmacol 64 (2002) 1037-1048
7. Dringen R., Gutterer J.M., and Hirrlinger J. Glutathione metabolism in brain metabolic interaction between astrocytes and neurons in the defense against reactive oxygen species. Eur J Biochem 267 (2000) 4912-4916
8. Vani M.L., and Reddy K.P. Effects of fluoride accumulation on some enzymes of brain and gastrocnemius muscle of mice. Fluoride 33 (2000) 17-26
9. Cheng X.T., Wang S.X., and Gao J.G. Analysis of MBP, NSEF content and CHE activity in brain tissue of rats with chronic fluorosis. Chin J Epidemiol 21 (2002) 358-364
10. Chouhan S., and Flora S.J.S. Effects of fluoride on the tissue oxidative stress and apoptosis in rats: biochemical assays supported by IR spectroscopy data. Toxicology 254 (2008) 61-67
11. Wasserman G.A., Liu X., Parvez F., Ahsan H., Factor-Litvak P., Van G.A., et al. Drinking water arsenic exposure and children's intellectual function in Araihazar, Bangladesh. Environ Health Perspect 112 (2004) 1329-1333
12. Li X.S., Zhi J.L., and Gao R.O. Effect of fluoride exposure on intelligence in children. Fluoride 28 (1995) 189-192
13. Flora S.J.S. Arsenic-induced oxidative stress and its reversibility following combined administration of N-acetylcysteine and meso 2, 3-dimercaptosuccinic acid in rats. Clin Exp Pharmacol Physiol 26 (1999) 865-869
14. Shila S., Kokilavani V., Subathra M., and Panneerselvam C. Brain regional responses in antioxidant system to alpha-lipoic acid in arsenic intoxicated rat. Toxicology 210 (2005) 25-36
15. Mittal M., and Flora S.J.S. Vitamin E supplementation protects oxidative stress during arsenic and fluoride antagonism in male mice. Drug Chem Toxicol 30 (2007) 263-281
16. Mittal M., and Flora S.J.S. Effects of individual and combined exposure to sodium arsenite and sodium fluoride on tissue oxidative stress, arsenic and fluoride levels in male mice. Chem Biol Inter 162 (2006) 128-139
17. Socci D.J., Bjugstad K.B., Jones H.C., Pattisapu J.V., and Arendash G.W. Evidence that oxidative stress is associated with the pathophysiology of inherited hydrocephalus in the H-Tx rat model. Exp Neurol 155 (1999) 109-117
18. Ohkawa H., Onishi N., and Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 95 (1979) 351-358
19. Kakkar P., Das B., and Viswanathan P.N. A modified spectrophotometric assay of superoxide dismutase. Ind J Biochem Biophys 21 (1984) 130-132
20. Sinha A.K. Colorimetric assay of catalase. Anal Biochem 47 (1972) 389-394
21. Flohe L., and Gunzler W.A. Assays of glutathione peroxidase. Meth Enzymol 105 (1984) 114-121
22. Hissin P.J., and Hilf R. A fluorometric method for the determination of oxidized and reduced glutathione in tissues. Anal Biochem 74 (1973) 214-216
23. Habig W.H., Pabst M.J., and Jakoby W.D. Glutathione transferase, the first enzymatic step in mecapturic acid formation. J Biol Chem 249 (1974) 7130-7139
24. Ornstein L. Disc electrophoresis: background and theory. Ann NY Acad Sci 121 (1964) 321-323
25. Scholl A., and Anders S. Electrophoretic variation of enzyme proteins in Platyfish and Swordtails (Poeciliidae, Teleostei). Arch Fur Genetik 46 (1973) 121-129
26. Ellman G.L., Courtney K.D., Andres V., and Featherstone R.M. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol 7 (1961) 88-95
27. Wurtman R.J., and Axelrod J. A sensitive and specific assay for the estimation of monoamine oxidase. Biochem Pharmacol 12 (1963) 1439-1445
28. Jacobwitz D.W., and Richardson J.S. Method for rapid determination of norepinephrine, dopamine and serotonin in the same brain region. Pharmacol Biochem Behav 8 (1978) 515-519
29. Sambrook J., Fritsch E.F., and Maniatis T. Molecular cloning: a laboratory manual. third edition 1 (2001), Cold Spring Harbor Laboratory Press 6.4-6.11
30. Smedley P.L., and Kinniburgh D.G. A review of the source, behaviour and distribution of arsenic in natural waters. Appl Geochem 17 (2002) 517-568
31. Ng J.C., Wang J., and Shraim A. A global health problem caused by arsenic from natural sources. Chemosphere 52 (2003) 1353-1359
32. Buchanan W.D. Toxicology of arsenic compounds (1962), Elsevier, Amsterdam 28-56
33. Tripathi N., Kannan G.M., Pant B.P., Jaiswal D.K., Malhotra P.R., and Flora S.J.S. Arsenic induced changes in certain neurotransmitters levels and their recoveries following chelation in rat whole brain. Toxicol Lett 92 (1997) 201-208
34. Itoh T., Zhang Y.F., Murai S., Saito H., Nagahama H., Miyaate H., et al. The effects of arsenic trioxide on brain monoamine metabolism and locomotor activity of mice. Toxicol Lett 54 (1990) 345-353
35. Chirumari K., and Reddy P.K. Dose-dependent effects of fluoride on neurochemical milieu in the hippocampus and neocortex of rat brain. Fluoride 40 (2007) 101-110
36. Ashani Y., Segev O., and Balan A. The effect of fluoride on the scavenging of organophosphates by human butyrylcholinesterase in buffer solutions and human plasma. Toxicol Appl Pharmacol 194 (2004) 90-99
37. Wang T.S., Kuo C.F., Jan K.Y., and Huang H. Arsenite induces apoptosis in Chinese hamster ovary cells by generation of reactive oxygen species. J Cell Physiol 169 (1996) 256-268
38. Wang J.D., Ge Y.M., Ning H.M., and Wang S.L. Effects of high fluoride and low iodine on oxidative stress and antioxidant defense of the brain in offspring rats. Fluoride 37 (2004) 264-270
39. Guan Z.Z., Xiao K.Q., Zeng X.Y., Cheng Y.H., Jiang S.F., and Wang Y.N. Changed cellular membrane lipid composition and lipid peroxidation of kidney in rats with chronic fluorosis. Arch Toxicol 74 (2000) 602-608
40. Takahashi M., Sato T., Shinohara F., Echigo S., and Rikiishi H. Possible role of glutathione in mitochondrial apoptosis of human oral squamous cell carcinoma caused by inorganic selenium compounds. Inter J Oncology 27 (2005) 489-495
41. Jones D.P. Redox potential of GSH/GSSG couple: assay and biological significance. Meth Enzymol 348 (2002) 93-112
42. Shivarajashankara Y.M., Shivashankara A.R., Gopalakrishna B.P., and Hanumanth R.S. Effect of fluoride intoxication on lipid Peroxidation and antioxidant systems in rats. Fluoride 34 (2001) 108-113
43. Dierickx P.J. Activation by sodium fluoride of drug-metabolizing enzymes in rat hepatoma-derived Fa32 cells. FEBS Lett 30 (1998) 185-188
44. Maher P., and Schubert D. Signaling by reactive oxygen species in the nervous system. Cell Mol Life Sci 57 (2002) 1287-1305
45. Wajcman H., and Galactéros F. Glucose 6-phosphate dehydrogenase deficiency: a protection against malaria and a risk for hemolytic accidents. C R Biologies 327 (2004) 711-720
46. Del Razo L.M., Quintanilla-Vega B., Brambila-Colombres E., Calderon-Aranda E.S., Manno M., and Albores A. Stress proteins induced by arsenic. Toxicol Appl Pharmacol 177 (2001) 132-148
47. Clarke M.W., Burnett J.R., and Croft K.D. Vitamin E in human health and disease. Crit Rev Clin Lab Sci 45 (2008) 417-450
48. Halliwell B., and Gutteridge J.M.C. Free radicals in biology and medicine vol. 3 (2002), Oxford University Press Inc., New York 105-145
49. Rajnarayan I., Sunderrajan K., and Shah T. Impacts of groundwater contamination with fluoride and arsenic: affliction severity, medical cost and wage loss in some villages of India. Inter J Rural Manag 3 (2007) 69-93
50. Jhala D.D., Chinoy N.J., and Rao M.V. Mitigating effects of some antidotes on fluoride and arsenic induced free radical toxicity in mice ovary. Food Chem Toxicol 46 (2008) 1138-1142
51. Nair S.B., Jhala D.D., and Chinoy N.J. Beneficial effects of certain antidotes in mitigating fluoride and / or arsenic induced hepatotoxicity in mice. Fluoride 37 (2004) 60-70
52. Yao H., and Wang G. Acute and chronic experimental studies on joint effect of fluoride and arsenic. Chin J Prevent Med 22 (1998) 284-286
53. Kao W.F., Deng J.F., Chiang S.C., Heard K., Yen D.H., Lu M.C., et al. A simple, safe, and efficient way to treat severe fluoride poisoning-oral calcium or magnesium. J Toxicol: Clin Toxicol 42 (2004) 33-40
54. Fujisawa C., Hagiwara R., and Ito Y. Dissolution equilibrium of arsenic pentafluoride in anhydrous hydrogen fluoride. J Fluorine Chem 107 (2001) 97-100
55. Schwerdtle T., Walter I., Mackiw I., and Hartwig A. Induction of oxidative DNA damage by arsenite and its trivalent and pentavalent methylated metabolites in cultured human cells and isolated DNA. Carcinogenesis 24 (2003) 967-974
56. Kyogoku Y., Tsuboi M., Shimanouchi T., and Watanabe T. Infrared spectra of formamide treated nucleic acids. J Mol Biol 3 (1961) 741-745
57. Kyogoku Y., Tsuboi M., and Shimanouchi T. Nucleic acids in deuterium oxide solution. Nature 189 (1961) 120-122