Effects of oral exposure to mining waste on in vivo dopamine release from rat striatum

Environmental Health Perspectives

Volumn 106, Issue 8, 1998, Pages 487-491

  Rodríguez, Verónica M ^a   Dufour, Leticia ^a   Carrizales, Leticia ^a   Díaz Barriga, Fernando ^a   Jiménez Capdaville, María E ^a  

^a UNIVERSIDAD AUTÓNOMA DE SAN LUIS POTOSÍ   (Mexico)

Author keywords

Chemical mixtures; Dopamine; Manganese; Metals; Mining waste; Toxic waste

Indexed keywords

3,4 DIHYDROXYPHENYLACETIC ACID; ARSENIC; ARSENITE SODIUM; BARIUM; CADMIUM; CHROMIUM; COPPER; DOPAMINE; HOMOVANILLIC ACID; LEAD; MANGANESE; METAL; NICKEL; POTASSIUM; ZINC;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; CORPUS STRIATUM; DEPOLARIZATION; DOPAMINE RELEASE; EXPOSURE; HEALTH HAZARD; INDUSTRIAL WASTE; MALE; MICRODIALYSIS; MINING; NEUROCHEMISTRY; NONHUMAN; PERFUSION; PRIORITY JOURNAL; RAT; STIMULATION;

ANIMALIA; VILLA;

EID: 0031658993     PISSN: 00916765     EISSN: None     Source Type: Journal    
DOI: 10.1289/ehp.98106487     Document Type: Article

References (41)

1. Informe de le Situación Generel en Materia de Equilibrio y Protección al Ambiente 1991-1992. Mexico, City:Sedesol (Secretaria de Desarrollo Social), 1993.
2. Montgomery EB. Heavy metals and the etiology of Parkinson's disease and other movement disorders. Toxicology 97:3-9 (1995).
3. Iregren A. Using psychological tests for the early detection of neurotoxic effects of low level manganese exposure. Neurotoxicology 15:671-677 (1994).
4. Defazio G, Soleo L, Zefferino R, Livrea P. Manganese toxicity In serumless dissociated mesencephalic and striatal primary culture. Brain Res Bull 40:257-262 (1996).
5. Ono J, Harada K, Kodaka R, Sakurai K, Tajiri H, Takagi Y, Nagai T, Harada T, Nihei A, Okada A. Manganese deposition In the brain during long-term total parenteral nutrition. J Parenter Enter Nutr 19:310-312 (1995).
6. Sloot WN, van der Sluijs-Gelling AJ, Gramsbergen JB. Selective lesions by manganese and extensive damage by iron after injection into rat striatum or hippocampus. J Neurochem 62:205-216 (1994).
7. Mejía JJ, Díaz-Barriga F, Calderón J, Ríos C, Jiménez-Capdeville ME. Effects of lead-arsenic combined exposure on central monoaminergic systems. Neurotoxicol Teratol 19:489-497 (1997).
8. Nagaraja TN, Desiraju T. Regional alterations in the levels of brain biogenic amines, glutamate, GABA and GAD activity due to chronic consumption of inorganic arsenic in developing and adult rats. Bull Environ Contam Toxicol 50:100-107 (1993).
9. Cory-Slechta DA, Pokora MJ, Fox RA, O'Mara DJ. Lead-induced changes in dopamine D1 sensitivity: modulation by drug discrimination training. Neurotoxicology 17:445-457 (1996).
10. Cory-Slechta DA. Relationships between lead-induced learning impairments and changes in dopaminergic, cholinergic, and glutamatergic neurotransmitter system functions. Annu Rev Pharmacol Toxicol 35:391-415 (1995).
11. Lasley SM, Greenland RD, Minnema DJ, Michaelson IA. Influence of chronic inorganic lead exposure on regional dopamine and 5-hydroxytryptamine turnover in rat brain. Neurochem Res 9:1675-1687 (1984).
12. Cory-Slechta DA, Pokora MJ, Preston RA. The effects of dopamine agonists on fixed interval schedule-controlled behavior are selectively altered by low-level lead exposure. Neurotoxicol Teratol 18:565-575 (1996).
13. Cory-Slechta DA, Widzowski DV, Pokora MJ. Functional alterations in dopamine systems assessed using drug discrimination procedures. Neurotoxicology 14:105-114 (1993).
14. Rehman S. Effects of lead on the behavioral complex stereotypes and regional brain dopamine levels in rats. Arch Environ Contam Toxicol 20:527-530 (1991).
15. Meredith PA, McIntosh MJ, Petty MA, Reid JL. Effects of lead exposure on rat brain catecholaminergic neurochemistry. Comp Biochem Physiol 89:215-219 (1988).
16. Govoni S, Memo M, Spano PF, Trabucchi M. Chronic lead treatment differentially affects dopamine synthesis in various brain areas. Toxicol 12:343-349 (1979).
17. Jadhav AL, Wellman PJ. Acute infusion of Pb causes dopamine release in rat brain (abstract). Fundam Appl Toxicol 36:933 (1997).
18. Rastogi RB, Merali Z, Singhal RL. Cadmium alters behaviour and the biosynthetic capacity for catecholamines and serotonin in neonatal rat brain. J Neurochem 28:789-794 (1977).
19. Gutiérrez-Reyes EY, Albores A, Ríos C. Cadmium stimulates dopamine release from rat striatal slices (abstract). Society of Toxicology 14:292 (1994).
20. Díaz-Barriga F. Riesgos para la salud y el ambiente por el manejo inadecuado de resiuos peligrosos. In: Residues Peligrosos (Rivero Serrano O, Garfias Vásquez M, González Martínez S, eds). México City:UNAM: 1996;196-229.
21. Ebdon L, Wilkinson JR, Jackson KW. A simple and sensitive continuous hydride generation system for determination of arsenic and selenium by atomic absortion and atomic fluorescence spectrometry. Anal Chim Acta 136:191-199 (1982).
22. Ediger DR. Determination of arsenic and selenium in biological and botanical materials by atomic absortion. Atomic Absortion Application Study No. 550. Norwalk, CT:Perkin-Elmer Co., 1973.
23. Subramanian KS, Méranger JC. Rapid hydride evolution-electrothermal atomisation atomic-absortion spectrophotometric method for determining arsenic and selenium in human kidney and liver. Analyst 107:157-162 (1982).
24. Vahter M, Berglund M, Slorach S, Friberg L, Saric M, Fujita M. Methods for integrated exposure monitoring of lead end cadmium. Environ Res 56:78-89 (1991).
25. Paxinos G, Watson C. The Rat Brain in Stereotaxic Coordinates. Marrickville, NSW:Academic Press Australia, 1982.
26. Mejía JJ, Carrizales L, Rodríguez VM, Jiménez-Capdeville ME, Díaz-Barriga F. Riesgos en salud por la exposición a residues mineros. Salud Publica de México (in press).
27. Freeman GB, Johnson JD, Killinger JM, et al. Biosvailability of arsenic in soil impacted by smelter activities following oral administration in rabbits. Fundam Appl Toxicol 21:83-88 (1993).
28. Freeman GB, Dill JA, Johnson JD, Kurtz PJ, Parham F, Matthews HB. Comparative absorption of leed from contaminated soil and lead selts by weening Fischer 344 rats. Fundam Appl Toxicol 33:109-119 (1996).
29. Calderón J, Navarro ME, Jiménez-Cepdeville ME, Golden A, Santos MA, Borja-Aburto V, Díaz-Barrige F. Growth deficit end chronic exposure to arsenic and lead modify neuropsychologicel responses in children. (Submitted).
30. Sharp T, Zetterström T, Ungerstedt U. An in vivo study of dopamine release and metabolism in rat brain regions using intracerebral dialysis. J Neurochem 47:113-122 (1986).
31. Osborne PG, O'Connor WT, Kehr J, Ungerstedt U. In vivo microdialysis of extracellular dopamine: GABA and acetylcholine from the dorsolateral striatum of awake freely moving rats by chronic microdialysis. J Neurosci Methods 37:93-102 (1991).
32. Imperato A, Di Chiara G. Trans-striatal dialysis coupled to reverse phase high performance liquid chromatography with electrochemical detection: a new method study of the in vivo release of endogenous dopamine and metabolites. J Neurosci 4:966-977 (1984).
33. Westerink BHC, Hofsteede HM, Damsma G, de Vries JB. The significance of extracellular calcium for the release of dopamine, acetylcholine and amino acids in conscious rats, evaluated by brain microdialysis. Naunyn-Schmiedebergs Arch Pharmacol 337:373-378 (1988).
34. Moghaddam B, Roth RH, Bunney BS. Characterization of dopamine release in the rat medial prsfrontal cortex as assesed by in vivo microdialysis: comparaison to the striatum. Neuroscience 36:669-676 (1990).
35. Westerink BHC, Tuinte MHJ. Chronic use of intracerebral dialysis for the in vivo measurement of 3,4- dihydroxyphenylethylamine and its metabolite 3,4-dihydroxyphenylacetic acid. J Neurochem 46:181-185 (1986).
36. Mark GP, Reda P, Pothos E, Hoebel BG. Effects of feeding and drinking on acetylcholine release in the nucleus accumbens: striatum, and hippocampus of freely behaving rats. J Neurochem 58:2269-2274 (1992).
37. Adams FS, Schwarting RKW, Boix F, Huston JP. Lateralized changes in behavior and striatal dopamine release following unilateral tactile stimulation of the perioral region: a microdialysis study. Brain Res 553:318-322 (1991).
38. Jiménez-Capdeville ME, Dykes RW. Daily changes in the release of acetylcholine from rat primary somatosensory cortex. Brain Res 625:152-158 (1993).
39. Inglis FM, Fibiger HC. Increases in hippocampal and frontal cortical acetylcholine release associated with presentation of sensory stimuli. Neuroscience 66:81-86 (1995).
40. Inglis FM, Day JC, Fibiger HC. Enhanced acetylcholine release in hippocampus and cortex during the anticipation and consumption of a palatable meal. Neuroscience 62:1049-1056 (1994).
41. Yang RSH, Hong HL, Boorman GA. Toxicology of chemical mixtures: experimental approaches, underlying concepts, and some results. Toxicol Lett 49:183-197 (1989).