Developmental exposure to pesticides zineb and/or endosulfan renders the nigrostriatal dopamine system more susceptible to these environmental chemicals later in life

NeuroToxicology

Volumn 28, Issue 4, 2007, Pages 727-735

  Jia, Zhenquan ^a   Misra, Hara P ^a,b  

^a VIRGINIA MARYLAND REGIONAL COLLEGE OF VETERINARY MEDICINE   (United States)

^b EDWARD VIA COLLEGE OF OSTEOPATHIC MEDICINE   (United States)

Author keywords

Chemical mixtures; Developmental; Dopamine; Endosulfan; Neurodegeneration; Parkinson's disease; Pesticides; Zineb

Indexed keywords

ACETYLCHOLINESTERASE; ALPHA SYNUCLEIN; DOPAMINE; ENDOSULFAN; NEUROTRANSMITTER; ZINEB;

ADULTHOOD; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BODY WEIGHT; BRAIN CORTEX; CONTROLLED STUDY; DEVELOPMENTAL STAGE; DOPAMINE BRAIN LEVEL; DOPAMINERGIC SYSTEM; ENVIRONMENTAL EXPOSURE; ENZYME ACTIVITY; JUVENILE; MALE; MOUSE; NERVE DEGENERATION; NIGRONEOSTRIATAL SYSTEM; NONHUMAN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN AGGREGATION;

ACETYLCHOLINESTERASE; AGE FACTORS; ANALYSIS OF VARIANCE; ANIMALS; ANIMALS, NEWBORN; BRAIN; DOPAMINE; DRUG INTERACTIONS; ENDOSULFAN; MALE; MICE; MICE, INBRED C57BL; MODELS, BIOLOGICAL; PESTICIDES; SYNUCLEINS; ZINEB;

MUS;

EID: 34447527453     PISSN: 0161813X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuro.2007.04.003     Document Type: Article

References (80)

1. Agrawal A.K., Anand M., Zaidi N.F., and Seth P.K. Involvement of serotonergic receptors in endosulfan neurotoxicity. Biochem Pharmacol 32 (1983) 3591-3593
2. Ahlbom J., Fredriksson A., and Eriksson P. Neonatal exposure to a type-I pyrethroid (bioallethrin) induces dose-response changes in brain muscarinic receptors and behaviour in neonatal and adult mice. Brain Res 645 (1994) 318-324
3. Aleksandrowicz D.R. Endosulfan poisoning and chronic brain syndrome. Arch Toxicol 43 (1979) 65-68
4. Alexander G.E., DeLong M.R., and Strick P.L. Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu Rev Neurosci 9 (1986) 357-381
5. Anand M., Agrawal A.K., Gopal K., Sur R.N., and Seth P.K. Endosulfan and cholinergic (muscarinic) transmission: effect on electroencephalograms and [3H]quinuclidinyl benzilate in pigeon brain. Environ Res 40 (1986) 421-426
6. Andersen J.K. Paraquat and iron exposure as possible synergistic environmental risk factors in Parkinson's disease. Neurotox Res 5 (2003) 307-313
7. Benke G.M., and Murphy S.D. The influence of age on the toxicity and metabolism of methyl parathion and parathion in male and female rats. Toxicol Appl Pharmacol 31 (1975) 254-269
8. Butterfield P.G., Valanis B.G., Spencer P.S., Lindeman C.A., and Nutt J.G. Environmental antecedents of young-onset Parkinson's disease. Neurology 43 (1993) 1150-1158
9. Buttke T.M., and Sandstrom P.A. Oxidative stress as a mediator of apoptosis. Immunol Today 15 (1994) 7-10
10. Campbell B.C., McLean C.A., Culvenor J.G., Gai W.P., Blumbergs P.C., Jakala P., et al. The solubility of alpha-synuclein in multiple system atrophy differs from that of dementia with Lewy bodies and Parkinson's disease. J Neurochem 76 (2001) 87-96
11. Carr R.L., Chambers H.W., Guarisco J.A., Richardson J.R., Tang J., and Chambers J.E. Effects of repeated oral postnatal exposure to chlorpyrifos on open-field behavior in juvenile rats. Toxicol Sci 59 (2001) 260-267
12. Cook J.E. Correlated activity in the CNS: a role on every timescale?. Trends Neurosci 14 (1991) 397-401
13. Correll L., and Ehrich M. A microassay method for neurotoxic esterase determinations. Fundam Appl Toxicol 16 (1991) 110-116
14. Cory-Slechta D.A., Thiruchelvam M., Richfield E.K., Barlow B.K., and Brooks A.I. Developmental pesticide exposures and the Parkinson's disease phenotype. Birth Defects Res A: Clin Mol Teratol 73 (2005) 136-139
15. Di Chiara G., Morelli M., and Consolo S. Modulatory functions of neurotransmitters in the striatum: ACh/dopamine/NMDA interactions. Trends Neurosci 17 (1994) 228-233
16. Dietert R.R., Lee J.E., and Bunn T.L. Developmental immunotoxicology: emerging issues. Hum Exp Toxicol 21 (2002) 479-485
17. el-Agnaf O.M., and Irvine G.B. Aggregation and neurotoxicity of alpha-synuclein and related peptides. Biochem Soc Trans 30 (2002) 559-565
18. Ellman G.L., Courtney K.D., Andres Jr. V., and Feather-Stone R.M. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol 7 (1961) 88-95
19. Eriksson P., Ahlbom J., and Fredriksson A. Exposure to DDT during a defined period in neonatal life induces permanent changes in brain muscarinic receptors and behaviour in adult mice. Brain Res 582 (1992) 277-281
20. Eriksson P., Nilsson-Hakansson L., Nordberg A., Aspberg A., and Fredriksson A. Neonatal exposure to DDT and its fatty acid conjugate: effects on cholinergic and behavioural variables in the adult mouse. Neurotoxicology 11 (1990) 345-354
21. Eriksson P., and Nordberg A. Effects of two pyrethroids, bioallethrin and deltamethrin, on subpopulations of muscarinic and nicotinic receptors in the neonatal mouse brain. Toxicol Appl Pharmacol 102 (1990) 456-463
22. Fasano M., Giraudo S., Coha S., Bergamasco B., and Lopiano L. Residual substantia nigra neuromelanin in Parkinson's disease is cross-linked to alpha-synuclein. Neurochem Int 42 (2003) 603-606
23. Ferraz H.B., Bertolucci P.H., Pereira J.S., Lima J.G., and Andrade L.A. Chronic exposure to the fungicide maneb may produce symptoms and signs of CNS manganese intoxication. Neurology 38 (1988) 550-553
24. Giorgi O., De Montis G., Porceddu M.L., Mele S., Calderini G., Toffano G., et al. Developmental and age-related changes in D1-dopamine receptors and dopamine content in the rat striatum. Brain Res 432 (1987) 283-290
25. Gomez L.E., Cueva-Rolon R., and Lehmann P.A. Disposition kinetics of HEPP in rats after intravenous, oral, and intraperitoneal administration. Correlation of plasma and brain levels with the anticonvulsant effect. Biopharm Drug Dispos 16 (1995) 77-89
26. Gorell J.M., Johnson C.C., Rybicki B.A., Peterson E.L., and Richardson R.J. The risk of Parkinson's disease with exposure to pesticides, farming, well water, and rural living. Neurology 50 (1998) 1346-1350
27. Gupta P.K. Endosulfan-induced neurotoxicity in rats and mice. Bull Environ Contam Toxicol 15 (1976) 708-713
28. Harbison R.D. Comparative toxicity of some selected pesticides in neonatal and adult rats. Toxicol Appl Pharmacol 32 (1975) 443-446
29. Hardy J. The relationship between Lewy body disease, Parkinson's disease, and Alzheimer's disease. Ann N Y Acad Sci 991 (2003) 167-170
30. Hashimoto M., and Masliah E. Alpha-synuclein in Lewy body disease and Alzheimer's disease. Brain Pathol 9 (1999) 707-720
31. Hedera P., Lerner A.J., Castellani R., and Friedland R.P. Concurrence of Alzheimer's disease, Parkinson's disease, diffuse Lewy body disease, and amyotrophic lateral sclerosis. J Neurol Sci 128 (1995) 219-224
32. Hodgson E., and Levi P.E. Pesticides: an important but underused model for the environmental health sciences. Environ Health Perspect 104 Suppl. 1 (1996) 97-106
33. Institute of Medicine (IOM). Gulf war and health. vol 2: Insecticides and solvents (2003), The National Academics Press, Washington, DC p. 412-8
34. Iyaniwura T.T. Mammalian toxicity and combined exposure to pesticides. Vet Hum Toxicol 32 (1990) 58-62
35. Kackar R., Srivastava M.K., and Raizada R.B. Assessment of toxicological effects of mancozeb in male rats after chronic exposure. Indian J Exp Biol 37 (1999) 553-559
36. Kalil RE. Synapse formation in the developing brain. Sci Am 1989; 261:76-9, 82-5.
37. Kimmel C.A., and Makris S.L. Recent developments in regulatory requirements for developmental toxicology. Toxicol Lett 120 (2001) 73-82
38. Kolomiets B.P., Deniau J.M., Glowinski J., and Thierry A.M. Basal ganglia and processing of cortical information: functional interactions between trans-striatal and trans-subthalamic circuits in the substantia nigra pars reticulata. Neuroscience 117 (2003) 931-938
39. Konno N. Neurotoxicity of organophosphorus and dithiocarbamate compounds. Nippon Eiseigaku Zasshi 57 (2003) 645-654
40. Lakshmana M.K., and Raju T.R. Endosulfan induces small but significant changes in the levels of noradrenaline, dopamine and serotonin in the developing rat brain and deficits in the operant learning performance. Toxicology 91 (1994) 139-150
41. Lee F.J., Liu F., Pristupa Z.B., and Niznik H.B. Direct binding and functional coupling of alpha-synuclein to the dopamine transporters accelerate dopamine-induced apoptosis. Faseb J 15 (2001) 916-926
42. Lipton S.A., and Kater S.B. Neurotransmitter regulation of neuronal outgrowth, plasticity and survival. Trends Neurosci 12 (1989) 265-270
43. Lotharius J., and Brundin P. Pathogenesis of Parkinson's disease: dopamine, vesicles and alpha-synuclein. Nat Rev Neurosci 3 (2002) 932-942
44. Manning-Bog A.B., McCormack A.L., Li J., Uversky V.N., Fink A.L., and Di Monte D.A. The herbicide paraquat causes up-regulation and aggregation of alpha-synuclein in mice: paraquat and alpha-synuclein. J Biol Chem 277 (2002) 1641-1644
45. Marchi M., Caviglia A., Paudice P., and Raiteri M. Calcium-dependent [3H]acetylcholine release and muscarinic autoreceptors in rat cortical synaptosomes during development. Neurochem Res 8 (1983) 621-628
46. Marsden C.D. The mysterious motor function of the basal ganglia: the Robert Wartenberg Lecture. Neurology 32 (1982) 514-539
47. Mattson M.P., Dou P., and Kater S.B. Outgrowth-regulating actions of glutamate in isolated hippocampal pyramidal neurons. J Neurosci 8 (1988) 2087-2100
48. McGrew D.M., Irwin I., and Langston J.W. Ethylenebisdithiocarbamate enhances MPTP-induced striatal dopamine depletion in mice. Neurotoxicology 21 (2000) 309-312
49. Mendoza C.E. Toxicity and effects of malathion on esterases of suckling albino rats. Toxicol Appl Pharmacol 35 (1976) 229-238
50. Moser V.C., Shafer T.J., Ward T.R., Meacham C.A., Harris M.W., and Chapin R.E. Neurotoxicological outcomes of perinatal heptachlor exposure in the rat. Toxicol Sci 60 (2001) 315-326
51. Nakai K., and Satoh H. Developmental neurotoxicity following prenatal exposures to methylmercury and PCBs in humans from epidemiological studies. Tohoku J Exp Med 196 (2002) 89-98
52. OTA. United States. Congress. Office of Technology Assessment. Neurotoxicity: identifying and controlling poisons of the nervous system: summary: new developments in neuroscience. Washington, DC: Congress of the U.S. For sale by the Supt. of Docs., U.S. G.P.O.; 1990.
53. Osmond C., and Barker D.J. Fetal, infant, and childhood growth are predictors of coronary heart disease, diabetes, and hypertension in adult men and women. Environ Health Perspect 108 Suppl. 3 (2000) 545-553
54. Perez R.G., Waymire J.C., Lin E., Liu J.J., Guo F., and Zigmond M.J. A role for alpha-synuclein in the regulation of dopamine biosynthesis. J Neurosci 22 (2002) 3090-3099
55. Rajput A.H., and Uitti R.J. Paraquat and Parkinson's disease. Neurology 37 (1987) 1820-1821
56. Ritz B., Yu F., Chapa G., and Fruin S. Effect of air pollution on preterm birth among children born in Southern California between 1989 and 1993. Epidemiology 11 (2000) 502-511
57. Rivera S., Rosa R., Martinez E., Sunol C., Serrano M.T., Vendrell M., et al. Behavioral and monoaminergic changes after lindane exposure in developing rats. Neurotoxicol Teratol 20 (1998) 155-160
58. Rivera S., Sanfeliu C., and Rodriguez-Farre E. Behavioral changes induced in developing rats by an early postnatal exposure to lindane. Neurotoxicol Teratol 12 (1990) 591-595
59. Sanchez-Ramos J.R., Hefti F., and Weiner W.J. Paraquat and Parkinson's disease. Neurology 37 (1987) 728
60. Savolainen K., and Hervonen H. Dithiocarbamate fungicides decrease histochemical reactivity of cholinesterases in the gut wall of the rat. Arch Toxicol Suppl 8 (1985) 272-276
61. Seaton T.A., Cooper J.M., and Schapira A.H. Free radical scavengers protect dopaminergic cell lines from apoptosis induced by complex I inhibitors. Brain Res 777 (1997) 110-118
62. Segawa M. Development of the nigrostriatal dopamine neuron and the pathways in the basal ganglia. Brain Dev 22 Suppl. 1 (2000) S1-S4
63. Semchuk K.M., Love E.J., and Lee R.G. Parkinson's disease and exposure to agricultural work and pesticide chemicals. Neurology 42 (1992) 1328-1335
64. Seth P.K., Saidi N.F., Agrawal A.K., and Anand M. Neurotoxicity of endosulfan in young and adult rats. Neurotoxicology 7 (1986) 623-635
65. Shafer T.J., Meyer D.A., and Crofton K.M. Developmental neurotoxicity of pyrethroid insecticides: critical review and future research needs. Environ Health Perspect 113 (2005) 123-136
66. Shatz C.J. Impulse activity and the patterning of connections during CNS development. Neuron 5 (1990) 745-756
67. Shin E.J., Jhoo J.H., Kim W.K., Jhoo W.K., Lee C., Jung B.D., et al. Protection against kainate neurotoxicity by pyrrolidine dithiocarbamate. Clin Exp Pharmacol Physiol 31 (2004) 320-326
68. Sidhu A., Wersinger C., and Vernier P. alpha-Synuclein regulation of the dopaminergic transporter: a possible role in the pathogenesis of Parkinson's disease. FEBS Lett 565 (2004) 1-5
69. Simmons J.E. Chemical mixtures: challenge for toxicology and risk assessment. Toxicology 105 (1995) 111-119
70. Slater A.F., Nobel C.S., and Orrenius S. The role of intracellular oxidants in apoptosis. Biochim Biophys Acta 1271 (1995) 59-62
71. Surgucheva I., Park B.C., Yue B.Y., Tomarev S., and Surguchov A. Interaction of myocilin with gamma-synuclein affects its secretion and aggregation. Cell Mol Neurobiol 25 (2005) 1009-1033
72. Takahashi R.N., Rogerio R., and Zanin M. Maneb enhances MPTP neurotoxicity in mice. Res Commun Chem Pathol Pharmacol 66 (1989) 167-170
73. Thiruchelvam M., Brockel B.J., Richfield E.K., Baggs R.B., and Cory-Slechta D.A. Potentiated and preferential effects of combined paraquat and maneb on nigrostriatal dopamine systems: environmental risk factors for Parkinson's disease?. Brain Res 873 (2000) 225-234
74. Thiruchelvam M., McCormack A., Richfield E.K., Baggs R.B., Tank A.W., Di Monte D.A., et al. Age-related irreversible progressive nigrostriatal dopaminergic neurotoxicity in the paraquat and maneb model of the Parkinson's disease phenotype. Eur J Neurosci 18 (2003) 589-600
75. Thiruchelvam M., Richfield E.K., Goodman B.M., Baggs R.B., and Cory-Slechta D.A. Developmental exposure to the pesticides paraquat and maneb and the Parkinson's disease phenotype. Neurotoxicology 23 (2002) 621-633
76. Tilson H.A. Developmental neurotoxicology of endocrine disruptors and pesticides: identification of information gaps and research needs. Environ Health Perspect 106 Suppl. 3 (1998) 807-811
77. Tilson H.A. Neurotoxicology risk assessment guidelines: developmental neurotoxicology. Neurotoxicology 21 (2000) 189-194
78. Voorn P., Kalsbeek A., Jorritsma-Byham B., and Groenewegen H.J. The pre- and postnatal development of the dopaminergic cell groups in the ventral mesencephalon and the dopaminergic innervation of the striatum of the rat. Neuroscience 25 (1988) 857-887
79. Zaidi N.F., Agrawal A.K., Anand M., and Seth P.K. Neonatal endosulfan neurotoxicity: behavioral and biochemical changes in rat pups. Neurobehav Toxicol Teratol 7 (1985) 439-442
80. Zhang J., Fitsanakis V.A., Gu G., Jing D., Ao M., Amarnath V., et al. Manganese ethylene-bis-dithiocarbamate and selective dopaminergic neurodegeneration in rat: a link through mitochondrial dysfunction. J Neurochem 84 (2003) 336-346