Protective effects of pre-germinated brown rice diet on low levels of Pb-induced learning and memory deficits in developing rat

Chemico-Biological Interactions

Volumn 184, Issue 3, 2010, Pages 484-491

  Zhang, Rong ^a   Lu, Hongzhi ^a   Tian, Su ^a   Yin, Jie ^a   Chen, Qing ^a   Ma, Li ^a   Cui, Shijie ^a   Niu, Yujie ^a  

^a HEBEI MEDICAL UNIVERSITY   (China)

Author keywords

Developing nervous system; GABA; Lead (Pb); Oxidative damage; Pre germinated brown rice

Indexed keywords

4 AMINOBUTYRIC ACID; 8 HYDROXYDEOXYGUANOSINE; GLUTAMIC ACID; LEAD; LEAD ACETATE; PHOSPHOLIPID HYDROPEROXIDE GLUTATHIONE PEROXIDASE; REACTIVE OXYGEN METABOLITE; SUPEROXIDE DISMUTASE;

AMNESIA; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANTIOXIDANT ACTIVITY; ARTICLE; BRAIN DEVELOPMENT; CONTROLLED STUDY; DIET SUPPLEMENTATION; ENZYME ACTIVITY; FEMALE; FLOW CYTOMETRY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HIPPOCAMPUS; LEARNING DISORDER; LIPID PEROXIDATION; MALE; MAZE TEST; NONHUMAN; OXIDATIVE STRESS; PASSIVE AVOIDANCE; RAT; RICE; WEANING;

ANIMALS; BRAIN; DEOXYGUANOSINE; DIET; FEMALE; GAMMA-AMINOBUTYRIC ACID; GLUTAMIC ACID; GLUTATHIONE PEROXIDASE; LEAD; LEAD POISONING; MALE; MALONDIALDEHYDE; MAZE LEARNING; MEMORY; ORYZA SATIVA; RATS; RATS, SPRAGUE-DAWLEY; REACTIVE OXYGEN SPECIES; SUPEROXIDE DISMUTASE;

ANIMALIA; RATTUS;

EID: 77949913988     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbi.2010.01.043     Document Type: Article

References (56)

1. Gilbert M.E., Lasley S.M. Developmental lead (Pb) exposure reduces the ability of the NMDA antagonist MK-801 to suppress long-term potentiation (LTP) in the rat dentate gyrus, in vivo. Neurotoxicol. Teratol. 2007, 29(3):385-393.
2. Beck B.D. An update on exposure and effects of lead. Fundam. Appl. Toxicol. 1992, 18:1-16.
3. Regan C.M. Lead-impaired neurodevelopment. Mechanisms and threshold values in the rodent. Neurotoxicol. Teratol. 1989, 11(6):533-537.
4. Bellinger D., Dietrich K.N. Low-level lead exposure and cognitive function in children. Pediatr. Ann. 1994, 23(11):600-605.
5. Gurer H., Ozygunes H., Saygin E., Ercal N. Antioxidant effect of taurine against lead-induced oxidative stress. Arch. Environ. Contam. Toxicol. 2001, 41(4):397-402.
6. Scortegagna M., Chikhale E., Hambauer I. Lead exposure increases oxidative stress in serum deprived E14 mesencephalic cultures. Role of metallothionine and glutathione. Restor. Neurol. Neurosci. 1998, 12(2-3):95-101.
7. Toscano C.D., Guilarte T.R. Lead neurotoxicity: from exposure to molecular effects. Brain Res. Brain Res. Rev. 2005, 49(3):529-554.
8. Chetty C.S., Vemuri M.C., Reddy G.R., Suresh C. Protective effect of 17-β-estradiol in human neurocellular models of lead exposure. NeuroToxicology 2007, 28:396-401.
9. Hammad T.A., Sexton M., Langenberg P. Relationship between blood lead and dietary iron intake in preschool children. A cross-sectional study. Ann. Epidemiol. 1996, 6(1):30-33.
10. Woolf A.D., Goldman R., Bellinger D.C. Update on the clinical management of childhood lead poisoning. Pediatr. Clin. North Am. 2007, 54(2):271-294.
11. Vázquez A., Peña de Ortiz S. Lead (Pb(+2)) impairs long-term memory and blocks learning-induced increases in hippocampal protein kinase C activity. Toxicol. Appl. Pharmacol. 2004, 200(1):27-39.
12. Butsata S., Siriamornpun S. Antioxidant capacities and phenolic compounds of the husk, bran and endosperm of Thai rice. Food Chem. 2010, 119:606-613.
13. Mamiya T, Asanuma T., Kise M., Ito Y., Mizukuchi A., Aoto H., Ukai M. Effects of pre-germinated brown rice on B-amyloid protein-induced learning and memory deficits in mice. Biol. Pharm. Bull. 2004, 27(7):1041-1045.
14. Bolin C.M., Basha R., Cox D., Zawia N.H., Maloney B., Lahiri D.K., Cardozo-Pelaez F. Exposure to lead (Pb) and the developmental origin of oxidative DNA damage in the aging brain. FASEB J. 2006, 20(6):788-790.
15. Usuki S., Ito Y., Morikawa K., Kise M., Ariga T., Rivner M., Yu R.K. Effect of pre-germinated brown rice intake on diabetic neuropathy in streptozotocin-induced diabetic rats. Nutr. Metab. (Lond.) 2007, 4:25.
16. Morris R. Developments of a water-maze procedure for studying spatial learning in the rat. J. Neurosci. Methods 1984, 11(1):47-60.
17. Urban I.J., Ontskul A., Croiset G., Cheng Y., de Wied D. A long-lasting increase and decrease in synaptic excitability in the rat lateral septum are associated with high and low shuttle box performance, respectively. Behav. Brain Res. 1995, 68(2):173-183.
18. Wang H., Joseph J.A. Quantifying cellular oxidative stress by dichlorofluorescein assay using microplate reader. Free Radic. Biol. Med. 1999, 27(5-6):612-616.
19. Zeng T., Guo F.F., Zhang C.L., Zhao S., Dou D.D., Gao X.C., Xie K.Q. The anti-fatty liver effects of garlic oil on acute ethanol-exposed mice. Chem. Biol. Interact. 2008, 176(2-3):234-242.
20. Huang X., Powell J., Mooney L.A., Li C., Frenkel K. Importance of complete DNA digestion in minimizing variability of 8-oxo-dG analyses. Free Radic. Biol. Med. 2001, 31(11):1341-1351.
21. Tomokuni K., Ogata M. Simple method for determination of urinary d-aminolevulinic acid as an index of lead exposure. Clin. Chem. 1972, 18:1534-1536.
22. Rahman S., Sultana S. Chemopreventive activity of glycyrrhizin on lead acetate mediated hepatic oxidative stress and its hyperproliferative activity in Wistar rats. Chem. Biol. Interact. 2006, 160(1):61-69.
23. Bergdahl I.A., Grubb A., Schütz A., Desnick R.J., Wetmur J.G., Sassa S., Skerfving S. Lead binding to delta-aminolevulinic acid dehydratase (ALAD) in human erythrocytes. Pharmacol. Toxicol. 1997, 81(4):153-158.
24. Hermes-Lima M., Pereira B., Bechara E.J. Are free radicals involved in lead poisoning?. Xenobiotica 1991, 21(8):1085-1090.
25. Yusof M., Yildiz D., Ercal N. N-acetyl-L-cysteine protects against delta-aminolevulinic acid-induced 8-hydroxydeoxyguanosine formation. Toxicol. Lett. 1999, 106(1):41-47.
26. Silbergeld E.K. Facilitative mechanisms of lead as a carcinogen. Mutat. Res. 2003, 533(1-2):121-133.
27. Marchetti C. Molecular targets of lead in brain neurotoxicity. Neurotox. Res. 2003, 5(3):221-236.
28. Moreira E.G., Vassilieff I., Vassilieff V.S. Developmental lead exposure: behavioral alterations in the short and long term. Neurotoxicol. Teratol. 2001, 23(5):489-495.
29. Cory-Slechta D.A., Weiss B. Efficacy of the chelating agent CaEDTA in reversing lead-induced changes in behavior. Neurotoxicology 1989, 10(4):685-697.
30. Bellinger D., Sloman J., Leviton A., Rabinowitz M., Needleman H.L., Aternaux C. Low-level lead exposure and children's cognitive function in the preschool years. Pediatrics 1991, 87(2):219-227.
31. Altmann L., Weinsberg F., Sveinsson K., Lilienthal H., Wiegand H., Winneke G. Impairment of long-term potentiation and learning following chronic lead exposure. Toxicol. Lett. 1993, 66(1):105-112.
32. Ma T., Chen H.H., Ho I.K. Effects of chronic lead (Pb) exposure on neurobehavioral function and dopaminergic neurotransmitter receptors in rats. Toxicol. Lett. 1999, 105(2):111-121.
33. Pachauri V., Saxena G., Mehta A., Mishra D., Flora S.J. Combinational chelation therapy abrogates lead-induced neurodegeneration in rats. Toxicol. Appl. Pharmacol. 2009, 240(2):255-264.
34. White L.D., Cory-Slechta D.A., Gilbert M.E., Tiffany-Castiglioni E., Zawia N.H., Virgolini M., Rossi-George A., Lasley S.M., Qian Y.C., Basha M.R. New and evolving concepts in the neurotoxicology of lead. Toxicol. Appl. Pharmacol. 2007, 225(1):1-27.
35. Struzyńska L., Sulkowski G. Relationships between glutamine, glutamate, and GABA in nerve endings under Pb-toxicity conditions. J. Inorg. Biochem. 2004, 98(6):951-958.
36. Gurer H., Ercal N. Can antioxidants be beneficial in the treatment of lead poisoning?. Free Radic. Biol. Med. 2000, 29(10):927-945.
37. Adonaylo V.N., Oteiza P.I. Lead intoxication: antioxidant defenses and oxidative damage in rat brain. Toxicology 1999, 135(2-3):77-85.
38. Zhang J., Wang X.F., Lu Z.B., Liu N.Q., Zhao B.L. The effects of meso-2,3-dimercaptosuccinic acid and oligomeric procyanidins on acute lead neurotoxicity in rat hippocampus. Free Radic. Biol. Med. 2004, 37(7):1037-1050.
39. Gurer H., Ozgunes H., Neal R., Spitz D.R., Ercal N. Antioxidant effects of N-acetylcysteine and succimer in red blood cells from Pb-exposed rats. Toxicology 1998, 128:181-189.
40. Hsu P.C., Liu M.Y., Hsu C.C., Chen L.Y., Guo Y.L. Effects of vitamin E and/or C on reactive oxygen species-related lead toxicity in the rat sperm. Toxicology 1998, 128(3):169-179.
41. Parrado J., Miramontes E., Jover M., Márquez J.C., Angeles Mejias M., Collantes De Teran L., Absi E., Bautista J. Prevention of brain protein and lipid oxidation elicited by a water-soluble oryzanol enzymatic extract derived from rice bran. Eur. J. Nutr. 2003, 42(6):307-314.
42. Miura D., Ito Y., Mizukuchi A., Kise M., Aoto H., Yagasaki K. Hypocholesterolemic action of pre-germinated brown rice in hepatoma-bearing rats. Life Sci. 2006, 79(3):259-264.
43. Patra R.C., Swarup D., Dwivedi S.K. Antioxidant effects of alpha tocopherol, ascorbic acid and l-methionine on lead induced oxidative stress to the liver, kidney and brain in rats. Toxicology 2001, 162(2):81-88.
44. Villeda-Hernández J, Barroso-Moguel R., Méndez-Armenta M., Nava-Ruíz C., Huerta-Romero R., Ríos C. Enhanced brain regional lipid peroxidation in developing rats exposed to low level lead acetate. Brain Res. Bull. 2001, 55(2):247-251.
45. Hsu P.C., Guo Y.L. Antioxidant nutrients and lead toxicity. Toxicology 2002, 180(1):33-44.
46. Sun D.Q., Li A.W., Li J., Li D.G., Li Y.X., Feng H., Gong M.Z. Changes of lipid peroxidation in carbon disulfide-treated rat nerve tissues and serum. Chem. Biol. Interact. 2009, 179:110-117.
47. Wang Q.S., Zhang C.L., Zhao X.L., Yu S.F., Xie K.Q. Malondialdehyde catalase as the serum biomarkers of allyl chloride-induced toxic neuropathy. Toxicology 2006, 227:36-44.
48. Fantone J.C., Ward P.A. Role of oxygen-derived free radicals and metabolites in leukocyte-dependent inflammatory reactions. Am. J. Pathol. 1982, 107(3):395-418.
49. Bechara E.J. Oxidative stress in acute intermittent porphyria and lead poisoning may be triggered by 5-aminolevulinic acid. Braz. J. Med. Biol. Res. 1996, 29(7):841-851.
50. Sakai T., Morita Y. Delta-aminolevulinic acid in plasma or whole blood as a sensitive indicator of lead effects, and its relation to the other heme-related parameters. Int. Arch. Occup. Environ. Health 1996, 68(2):126-132.
51. Yusof M, Yildiz D., Ercal N. N-acetyl-l-cysteine protects against delta-aminolevulinic acid-induced 8-hydroxydeoxyguanosine formation. Toxicol. Lett. 1999, 106(1):41-47.
52. Merzenich H., Hartwig A., Ahrens W., Beyersmann D., Schlepegrell R., Scholze M., Timm J., Jöckel K.H. Biomonitoring on carcinogenic metals and oxidative DNA damage in a cross-sectional study. Cancer Epidemiol. Biomarkers Prev. 2001, 10(5):515-522.
53. Antonio-García M.T., Massó-Gonzalez E.L. Toxic effects of perinatal lead exposure on the brain of rats: involvement of oxidative stress and the beneficial role of antioxidants. Food Chem. Toxicol. 2008, 46(6):2089-2095.
54. Aykin-Burns N., Ercal N. Effects of selenocystine on lead-exposed Chinese hamster ovary (CHO) and PC-12 cells. Toxicol. Appl. Pharmacol. 2006, 214(2):36-43.
55. Rose H.E., Quarterman J. Dietary fibers and heavy metal retention in the rat. Environ. Res. 1987, 42(1):166-175.
56. Ou S., Gao K., Li Y. An in vitro study of wheat bran binding capacity for Hg, Cd, and Pb, J. Agric. Food Chem. 1999, 47(11):4714-4717.